79 jobs found in Basel-Stadt

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    • basel, basel-stadt
    • temp to perm
    Für wiederkehrende und längere Einsätze und unserem Pool suchen wirKoch / KöchinAufgabenZubereitung und anrichten einzelner Gerichte sowie ganzer Menüs und à la carteVerantwortung auf allen PostenKontrolle und Verwaltung des WarenbestandsVerantwortung für die Einhaltung der strengen Hygienevorschriften gemäss HACCP
    Für wiederkehrende und längere Einsätze und unserem Pool suchen wirKoch / KöchinAufgabenZubereitung und anrichten einzelner Gerichte sowie ganzer Menüs und à la carteVerantwortung auf allen PostenKontrolle und Verwaltung des WarenbestandsVerantwortung für die Einhaltung der strengen Hygienevorschriften gemäss HACCP
    • basel, basel-stadt
    • temporary
    Wenn du dir neben deinem Studium etwas dazu verdienen willst oder nach einer Möglichkeit suchst dein Taschengeld etwas aufzustockenDann bist du genau richtig bei uns!Für unseren Mitarbeiter-Pool suchen wir flexible und motivierteservicemitarbeiter (m/w)Hauptaufgaben:bedienen und beraten der Gästeführen einer eigenen Stationmithilfe bei Banketten, Caterings, Events oder in Kantinenmise en place Aufgabenallgemeine Aufräum- und Reinigungsarbeiten
    Wenn du dir neben deinem Studium etwas dazu verdienen willst oder nach einer Möglichkeit suchst dein Taschengeld etwas aufzustockenDann bist du genau richtig bei uns!Für unseren Mitarbeiter-Pool suchen wir flexible und motivierteservicemitarbeiter (m/w)Hauptaufgaben:bedienen und beraten der Gästeführen einer eigenen Stationmithilfe bei Banketten, Caterings, Events oder in Kantinenmise en place Aufgabenallgemeine Aufräum- und Reinigungsarbeiten
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden im Raum Liestal, suchen wir per sofort oder nach Vereinbarung einen Elektroinstallateur (m/w) 100%Deine Aufgaben-Unterhalt und Reparatur von Elektroinstallationen-Installation von Elektroanlagen, Hausanschluss bis zur Steckdose-Materialmengenberechnungen-Arbeiten nach technischen Plänen und Schemata-Service- und Reparaturdienst
    Exklusiv für unseren Kunden im Raum Liestal, suchen wir per sofort oder nach Vereinbarung einen Elektroinstallateur (m/w) 100%Deine Aufgaben-Unterhalt und Reparatur von Elektroinstallationen-Installation von Elektroanlagen, Hausanschluss bis zur Steckdose-Materialmengenberechnungen-Arbeiten nach technischen Plänen und Schemata-Service- und Reparaturdienst
    • basel, basel-stadt
    • temp to perm
    Wir suchenLogistiker (m/w)Aufgaben· Be- und Entladen von LKW· Kommissionierung, Labeln und Verpackung der Ware· Eingangskontrolle und Einlagern von Waren· Kontrolle der ausgehenden Sendungen· Bearbeiten von Retouren· Mitarbeit bei der Inventurdurchführung· Disponieren der eingehenden und ausgehenden Sendungen· Diverse administrative Tätigkeiten
    Wir suchenLogistiker (m/w)Aufgaben· Be- und Entladen von LKW· Kommissionierung, Labeln und Verpackung der Ware· Eingangskontrolle und Einlagern von Waren· Kontrolle der ausgehenden Sendungen· Bearbeiten von Retouren· Mitarbeit bei der Inventurdurchführung· Disponieren der eingehenden und ausgehenden Sendungen· Diverse administrative Tätigkeiten
    • basel, basel-stadt
    • contract
    For our customer, one of the world's leading pharmaceutical company in Basel, Switzerland, we are looking for a committed and reliable personality as a Data Anonymization Specialist .As a skilled Biomedical Data Curation and Anonymization Specialist you will support research and development projects in digital pathology. You will curate pathology image datasets and associated metadata so that they are well organized and accurate, and will apply data anonymization tools to anonymize digital pathology images and associated image, clinical and genetic metadata. You will work with multiple stakeholders to locate, transfer, and prepare the data for use by pathologists and data scientists.Tasks and Responsibilities:You will be responsible for ensuring digital pathology (DP) images and multidimensional associated metadata ingested into the DP storage platform are well organized, anonymized and meet technical quality standards required for DP algorithm development. The role will not require visual assessment of image content; however, previous experience working with DP or other imaging modalities will help the successful candidate accomplish the listed tasks:Run data anonymization algorithms on digital pathology images, image metadata, clinical data, and genetic dataContribute to the maintenance and optimization of digital pathology image/data anonymization algorithmsUse and improve metadata storage and management toolsManage digital pathology project data, curate image, clinical, and genetic metadataSupport data transfers and ingestion from internal and external parties, carry out technical quality control on ingested dataCommunicate with external data providers about data transfer requirements, share technical issues with vendors, oversee and contribute to their resolutionWork closely with groups across the organization to locate and access data from diverse company internal systemsMust Haves:Min. Master’s degree in Computer Science, Data Science, or related field, or 3+ years working experience in a data curation, data anonymization or data management role Experience with general tools and techniques used in anonymization workflows and practical experience with R and PythonDemonstrated communication skills of technical information, both understanding and expressing requirements from stakeholders with a high level of bioinformatics expertise (i.e. an ability to both work with and communicate about large datasets containing imaging, clinical, demographic, genetic etc. data) Practical experience with cloud services (AWS, Azure, GCP) Experience in managing large datasetsBusiness fluency in English (written and spoken)Ability to work independently, follow up on verbal discussions with concrete action steps, and take initiativeStrong organizational skills with meticulous attention to detailOpen to embrace new ideas and ability to operate in a flexible mannerStrong interpersonal skills and a consultative mindset, with the ability to influence without direct authority, and to develop strong partnerships“Self-starter”; strong sense of responsibility with demonstrable comfort in an entrepreneurial environmentGood problem-solving ability, breaking down complex problems into distinct parts, managing uncertainty, understanding, anticipating interdependencies.Nice to Haves:Prior experience with digital pathology or imaging and clinical dataFamiliarity with Data modelingFamiliarity with database software and organizational systems such as LIMSIf this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today. Please note that we are only considering applications from Swiss and EU-27/EFTA nationals or Swiss work permit holders for our open positions in Switzerland.
    For our customer, one of the world's leading pharmaceutical company in Basel, Switzerland, we are looking for a committed and reliable personality as a Data Anonymization Specialist .As a skilled Biomedical Data Curation and Anonymization Specialist you will support research and development projects in digital pathology. You will curate pathology image datasets and associated metadata so that they are well organized and accurate, and will apply data anonymization tools to anonymize digital pathology images and associated image, clinical and genetic metadata. You will work with multiple stakeholders to locate, transfer, and prepare the data for use by pathologists and data scientists.Tasks and Responsibilities:You will be responsible for ensuring digital pathology (DP) images and multidimensional associated metadata ingested into the DP storage platform are well organized, anonymized and meet technical quality standards required for DP algorithm development. The role will not require visual assessment of image content; however, previous experience working with DP or other imaging modalities will help the successful candidate accomplish the listed tasks:Run data anonymization algorithms on digital pathology images, image metadata, clinical data, and genetic dataContribute to the maintenance and optimization of digital pathology image/data anonymization algorithmsUse and improve metadata storage and management toolsManage digital pathology project data, curate image, clinical, and genetic metadataSupport data transfers and ingestion from internal and external parties, carry out technical quality control on ingested dataCommunicate with external data providers about data transfer requirements, share technical issues with vendors, oversee and contribute to their resolutionWork closely with groups across the organization to locate and access data from diverse company internal systemsMust Haves:Min. Master’s degree in Computer Science, Data Science, or related field, or 3+ years working experience in a data curation, data anonymization or data management role Experience with general tools and techniques used in anonymization workflows and practical experience with R and PythonDemonstrated communication skills of technical information, both understanding and expressing requirements from stakeholders with a high level of bioinformatics expertise (i.e. an ability to both work with and communicate about large datasets containing imaging, clinical, demographic, genetic etc. data) Practical experience with cloud services (AWS, Azure, GCP) Experience in managing large datasetsBusiness fluency in English (written and spoken)Ability to work independently, follow up on verbal discussions with concrete action steps, and take initiativeStrong organizational skills with meticulous attention to detailOpen to embrace new ideas and ability to operate in a flexible mannerStrong interpersonal skills and a consultative mindset, with the ability to influence without direct authority, and to develop strong partnerships“Self-starter”; strong sense of responsibility with demonstrable comfort in an entrepreneurial environmentGood problem-solving ability, breaking down complex problems into distinct parts, managing uncertainty, understanding, anticipating interdependencies.Nice to Haves:Prior experience with digital pathology or imaging and clinical dataFamiliarity with Data modelingFamiliarity with database software and organizational systems such as LIMSIf this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today. Please note that we are only considering applications from Swiss and EU-27/EFTA nationals or Swiss work permit holders for our open positions in Switzerland.
    • basel, basel-stadt
    • contract
    We are currently supporting a leading pharmaceutical company in the area of Basel, in their search for an experienced Senior Project Manager for Pharma Informatics (IT).Tasks and Responsibilities:As a Project Manager, you will assemble, guide, empower and serve the team through excellence in project delivery resulting in value creation for our business and eventually, our patients. You will be responsible for leading a team to deliver project outcomes, products and services in a complex IT environment by selecting the best project delivery method (i.e. Agile principles and practices or Waterfall) that best fit the business needs. Therefore, the Project Manager can take on one, or a combination, of the following roles in a squad, project or program: Program Manager, Project Manager, Squad Lead, Agile Coach or Scrum MasterAs part of one or more of those roles, you will be:Engage with Leadership, both business and IT, to collaborate on the delivery of value at a rate that is sustainable and digestible for the team and businessEnsure promised business value is being earned by leveraging the value creation or value maintenance frameworkOrchestrate the formation of a squad and once established, closely interact with the product owner, partners and the development teamSource of skills that are supplied by Pharma Informatics or other Technology partnersGuide the squad on self-organising to fill in the intentional gaps left in the Agile/Scrum frameworksCoach the team to learn and adopt agreed ways of working and reacting to potential challenges and questionsYour Profile:Has an agile mindset with ability to pivot between roles and approaches based on team needsChampions Agile principles and practices within the squad and leads by exampleHas a strong focus on delivering MVP’s, focused on incremental value rather than perfection.Has strong soft skills typically required in stakeholder engagement (empowering people, influencing, negotiation, conflict management)Exhibits servant leadership style towards the product owner, scrum master, development team and the wider organizationThis is a challenging and exciting job opportunity. Are you ready for it? Then don`t hesitate to send your application.
    We are currently supporting a leading pharmaceutical company in the area of Basel, in their search for an experienced Senior Project Manager for Pharma Informatics (IT).Tasks and Responsibilities:As a Project Manager, you will assemble, guide, empower and serve the team through excellence in project delivery resulting in value creation for our business and eventually, our patients. You will be responsible for leading a team to deliver project outcomes, products and services in a complex IT environment by selecting the best project delivery method (i.e. Agile principles and practices or Waterfall) that best fit the business needs. Therefore, the Project Manager can take on one, or a combination, of the following roles in a squad, project or program: Program Manager, Project Manager, Squad Lead, Agile Coach or Scrum MasterAs part of one or more of those roles, you will be:Engage with Leadership, both business and IT, to collaborate on the delivery of value at a rate that is sustainable and digestible for the team and businessEnsure promised business value is being earned by leveraging the value creation or value maintenance frameworkOrchestrate the formation of a squad and once established, closely interact with the product owner, partners and the development teamSource of skills that are supplied by Pharma Informatics or other Technology partnersGuide the squad on self-organising to fill in the intentional gaps left in the Agile/Scrum frameworksCoach the team to learn and adopt agreed ways of working and reacting to potential challenges and questionsYour Profile:Has an agile mindset with ability to pivot between roles and approaches based on team needsChampions Agile principles and practices within the squad and leads by exampleHas a strong focus on delivering MVP’s, focused on incremental value rather than perfection.Has strong soft skills typically required in stakeholder engagement (empowering people, influencing, negotiation, conflict management)Exhibits servant leadership style towards the product owner, scrum master, development team and the wider organizationThis is a challenging and exciting job opportunity. Are you ready for it? Then don`t hesitate to send your application.
    • basel, basel-stadt
    • contract
    Are you an experienced Project Manager in IT and you are looking for a long-term contracting challenge in Basel? Then do not hesitate to apply!This Senior Project Support Management position will be responsible for co-managing the main activities on a global scale and supporting the integration of this project with other program initiatives. Together with this, the position will be very focused on the End-to-End integration of the overall solution across the different work streams and for that reason the appropriate candidate must have excellent communication and socialization skills to build a strong network in Aspire and outside Aspire.his position is also expected to provide timely status reports to all stakeholders and escalate issues to the appropriate management level. Additionally, this position must effectively manage the projects across global locations and time zones and be able to travel internationally as needed. Tasks and responsibilities:Execution of multiple initiatives across the Global Template project and beyond, including interaction with other multidisciplinary teamsCoordinate the project activities with 3rd party software vendor and/or System Integrator resources as needed to ensure project delivery and the different work streams when requiredManage relationships with various technology and business communities to achieve project objectivesFacilitate project management activities across the entire project management methodologyTrack progress of activities against baseline scheduleConduct risk management planning, identification, analysis and monitoring on projects, formulating risk mitigation strategies and recommend solutionsManage the processes required to ensure timely and appropriate generation, collection, distribution, storage, retrieval, and ultimate disposition of project information and documentation necessary for successful communications across all stakeholders and any required updates to living system documents for validated systemsActively seek opportunities to and mentor to other project managersPromote and hold multidisciplinary conversations/discussion between different work streams and teams outside ASPIRESupport the definition and implementation of Data Governance around Aspire and group wiseSupport the implementation of an integrated view of the business through E2E scenarios following the business guidelinesSuggest improvements where necessary / appropriate to improve operational efficienciesEngage with interested parties within the company, verify business use cases and provide expert consultancy. Guide new projects and help our internal customers to understand how they benefit the mostPartner actively with Business as well as IT Business Partners Must haves:Min. Bachelor's degree in Computer Sciences, Life Sciences, Business, Analytics and Reporting; or equivalent work experience or any other higher certification 10+ years of experience as a successful Information Technology Project Manager with a strong IT BackgroundExperience in using structured project management processes with deep understanding of various SDLCs (Waterfall, Agile, iterative, etc.), SAP A&R technology and solutions and new Analytics implementation challenges  Experience in Change Management is needed Proven leadership abilities, experience in leading multifunctional teams Excellent oral and written communication skills English fluent (C1), German is a plusAbility to manage relationships with various technology and business communities to achieve project objectivesVery experience communicator which is used to talk with different stakeholders on different levels and feels confident in project setupsProven ability to obtain results in a global, matrix environmentDemonstrated success communicating across a variety of audiences, including business people and technologists (both up and down the organization)Exceptional listening, problem solving, negotiation, and facilitation skillsDemonstrated success handling initiatives of significant complexity and risk Nice to have:Experience within the Pharmaceutical and BioTech industryExperience managing IT projects in GxP validated environmentsCertification as Project Manager or Scrum Master is a plus If this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today.
    Are you an experienced Project Manager in IT and you are looking for a long-term contracting challenge in Basel? Then do not hesitate to apply!This Senior Project Support Management position will be responsible for co-managing the main activities on a global scale and supporting the integration of this project with other program initiatives. Together with this, the position will be very focused on the End-to-End integration of the overall solution across the different work streams and for that reason the appropriate candidate must have excellent communication and socialization skills to build a strong network in Aspire and outside Aspire.his position is also expected to provide timely status reports to all stakeholders and escalate issues to the appropriate management level. Additionally, this position must effectively manage the projects across global locations and time zones and be able to travel internationally as needed. Tasks and responsibilities:Execution of multiple initiatives across the Global Template project and beyond, including interaction with other multidisciplinary teamsCoordinate the project activities with 3rd party software vendor and/or System Integrator resources as needed to ensure project delivery and the different work streams when requiredManage relationships with various technology and business communities to achieve project objectivesFacilitate project management activities across the entire project management methodologyTrack progress of activities against baseline scheduleConduct risk management planning, identification, analysis and monitoring on projects, formulating risk mitigation strategies and recommend solutionsManage the processes required to ensure timely and appropriate generation, collection, distribution, storage, retrieval, and ultimate disposition of project information and documentation necessary for successful communications across all stakeholders and any required updates to living system documents for validated systemsActively seek opportunities to and mentor to other project managersPromote and hold multidisciplinary conversations/discussion between different work streams and teams outside ASPIRESupport the definition and implementation of Data Governance around Aspire and group wiseSupport the implementation of an integrated view of the business through E2E scenarios following the business guidelinesSuggest improvements where necessary / appropriate to improve operational efficienciesEngage with interested parties within the company, verify business use cases and provide expert consultancy. Guide new projects and help our internal customers to understand how they benefit the mostPartner actively with Business as well as IT Business Partners Must haves:Min. Bachelor's degree in Computer Sciences, Life Sciences, Business, Analytics and Reporting; or equivalent work experience or any other higher certification 10+ years of experience as a successful Information Technology Project Manager with a strong IT BackgroundExperience in using structured project management processes with deep understanding of various SDLCs (Waterfall, Agile, iterative, etc.), SAP A&R technology and solutions and new Analytics implementation challenges  Experience in Change Management is needed Proven leadership abilities, experience in leading multifunctional teams Excellent oral and written communication skills English fluent (C1), German is a plusAbility to manage relationships with various technology and business communities to achieve project objectivesVery experience communicator which is used to talk with different stakeholders on different levels and feels confident in project setupsProven ability to obtain results in a global, matrix environmentDemonstrated success communicating across a variety of audiences, including business people and technologists (both up and down the organization)Exceptional listening, problem solving, negotiation, and facilitation skillsDemonstrated success handling initiatives of significant complexity and risk Nice to have:Experience within the Pharmaceutical and BioTech industryExperience managing IT projects in GxP validated environmentsCertification as Project Manager or Scrum Master is a plus If this role excites you, and you feel you could take this next challenge in your career, then I look forward to receiving your application today.
    • basel, basel-stadt
    • temporary
    We are looking for a Capex Procurement Lead Buyer (m/f/d) for Lonza AG (100%). This is a temporary position for 12 months, with an option of extension. Remote work within Switzerland is possible, with regular days on site in Visp. Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of. Key responsibilities: Supporting Procurement Category Manager to:Develop and execute a category strategy for Engineering Services that matches supply market capabilities with Lonza business needs.Lead supplier relationship management (SRM) and supplier development activities to ensure reliable supply and maximize the full value of supplier relationships.Drive supplier performance, compliance and accountability through supplier scorecards and performance metricsDevelop supply risk management strategies and drive development and implementation of appropriate risk mitigation plans.Manage relationships with suppliers acting as the primary point of contact for assigned suppliers.Work closely with Project Procurement colleagues to ensure category strategies are translated into project execution plans.Plan, lead and execute negotiations of commercial terms and contracting for framework, master and other major supply agreements.Ensure project sourcing objectives, actions and priorities are aligned both within Global Capex Procurement, Global Engineering and project stakeholders.Work closely with key stakeholders to develop cost reduction strategies and implementation plans that meet projects / business needs.Report savings monthly as well as maintain the project savings pipeline.Project procurement tasks, including:Procurement of services (consulting, engineering and planning) for the assigned investment projects.Development of project purchasing strategy, execution and coordination of procurement activities for assigned investment projects. Drive awareness of supply issues within the project, clarifying business impact and lead resolution plans.
    We are looking for a Capex Procurement Lead Buyer (m/f/d) for Lonza AG (100%). This is a temporary position for 12 months, with an option of extension. Remote work within Switzerland is possible, with regular days on site in Visp. Today, Lonza is a global leader in life sciences operating across three continents. While Lonza works in science, there's no magic formula to how they do it. Their greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, they let their people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work Lonza wants to be part of. Key responsibilities: Supporting Procurement Category Manager to:Develop and execute a category strategy for Engineering Services that matches supply market capabilities with Lonza business needs.Lead supplier relationship management (SRM) and supplier development activities to ensure reliable supply and maximize the full value of supplier relationships.Drive supplier performance, compliance and accountability through supplier scorecards and performance metricsDevelop supply risk management strategies and drive development and implementation of appropriate risk mitigation plans.Manage relationships with suppliers acting as the primary point of contact for assigned suppliers.Work closely with Project Procurement colleagues to ensure category strategies are translated into project execution plans.Plan, lead and execute negotiations of commercial terms and contracting for framework, master and other major supply agreements.Ensure project sourcing objectives, actions and priorities are aligned both within Global Capex Procurement, Global Engineering and project stakeholders.Work closely with key stakeholders to develop cost reduction strategies and implementation plans that meet projects / business needs.Report savings monthly as well as maintain the project savings pipeline.Project procurement tasks, including:Procurement of services (consulting, engineering and planning) for the assigned investment projects.Development of project purchasing strategy, execution and coordination of procurement activities for assigned investment projects. Drive awareness of supply issues within the project, clarifying business impact and lead resolution plans.
    • basel, basel-stadt
    • temporary
    Du bist eine neugierige, proaktive und teamfähige Person, die sich mit Gourmetkaffee von der Marke Nespresso identifiziert und bei Kunden als Botschafter die Philosophie vermittelst. Für den Standort in Basel suchen wir engagierte Verkäufer / Promoter für Nespresso (m/w) 40-60%Deine Aufgaben:Du begrüsst und informierst Kunden proaktiv als Erstkontakt über die Marke Nespresso und schaffst so ein unvergessliches KauferlebnisDu führst Kaffeedegustationen durch und gewährleistest eine fachkompetente Beratung und Verkauf von Nespresso Kaffee und Maschinen Durch deine offene Art kann der Assessoires, Maschinen und Kaffee Verkauf gesteigert werdenBei Fragen zu einfachen Störungen kannst du den Kunden kompetent beraten und eine Lösung anbietenDie monatliche Führung von Verkaufsrapporten, administrativen Aufgaben sowie die Sicherstellung der Sauberkeit des Verkaufspunkts gehören ebenfalls zu deinen Aufgaben
    Du bist eine neugierige, proaktive und teamfähige Person, die sich mit Gourmetkaffee von der Marke Nespresso identifiziert und bei Kunden als Botschafter die Philosophie vermittelst. Für den Standort in Basel suchen wir engagierte Verkäufer / Promoter für Nespresso (m/w) 40-60%Deine Aufgaben:Du begrüsst und informierst Kunden proaktiv als Erstkontakt über die Marke Nespresso und schaffst so ein unvergessliches KauferlebnisDu führst Kaffeedegustationen durch und gewährleistest eine fachkompetente Beratung und Verkauf von Nespresso Kaffee und Maschinen Durch deine offene Art kann der Assessoires, Maschinen und Kaffee Verkauf gesteigert werdenBei Fragen zu einfachen Störungen kannst du den Kunden kompetent beraten und eine Lösung anbietenDie monatliche Führung von Verkaufsrapporten, administrativen Aufgaben sowie die Sicherstellung der Sauberkeit des Verkaufspunkts gehören ebenfalls zu deinen Aufgaben
    • basel, basel-stadt
    • contract
    Do you want to work in a big pharmaceutical company? Do you have experience in GCP and Pulmonary Hypertension Therapeutic Area or Cardiovascular/Cardiopulmonary? You should then read the following lines! Our client, based in Basel area, is looking for a Clinical Project Physician for a one year contract. The Project Physician is a responsible member of a clinical team dedicated to the development and execution of medical strategies and the clinical and operational implementation of a complex compound program. The Project Physician provides active medical and scientific contribution to a cross-functional clinical team. The Project Physician provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes ownership for the content of clinical study reports and relevant documents for regulatory filings. Team matrix interactions include project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management,medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology and other scientific and business related disciplines. The Project Physician may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area Essential Functions: Responsible for medical monitoring/reporting and company safety officer activitiesWorks on clinical development plans, trial protocols and takes ownership of clinical study reportsEvaluates adverse events (pre and post-marketing) for relationship to treatmentAssists Regulatory Affairs in determining requirements for any corrective actions or health authority reportingMay act as a medical contact at the company for health authorities concerning clinical/medical issuesInterprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissionsClose interactions with Project Scientists and Physicians across programs Other Responsibilities : Assists Regulatory Affairs in the development of drug regulatory strategiesHelps explore and evaluate new product ideas to assist in identifying new market opportunitiesSupport general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillanceParticipate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.Reviews medical literature and related new technologiesMay be asked to assess medical publications emerging from the Team and its affiliatesMay be responsible, with appropriate colleagues, for review of Company advertising and promotional materials Candidate Profile: MD (or equivalent) in relevant area with appropriate post-doctoral training and certificationExperience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filingsSpecific experience in phase II and III studies is a strong advantage.Submission experience a strong advantage.Experience in medical review.Ideally previous experience in the Pulmonary Hypertension Therapeutic Area, otherwise Cardiovascular/Cardiopulmonary experience is appreciated.English Fluent Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
    Do you want to work in a big pharmaceutical company? Do you have experience in GCP and Pulmonary Hypertension Therapeutic Area or Cardiovascular/Cardiopulmonary? You should then read the following lines! Our client, based in Basel area, is looking for a Clinical Project Physician for a one year contract. The Project Physician is a responsible member of a clinical team dedicated to the development and execution of medical strategies and the clinical and operational implementation of a complex compound program. The Project Physician provides active medical and scientific contribution to a cross-functional clinical team. The Project Physician provides input to the clinical development plan, works on the development of the clinical trial protocol, clinical trial materials, and takes ownership for the content of clinical study reports and relevant documents for regulatory filings. Team matrix interactions include project management, finance, legal, quality assurance, quality monitoring & compliance, clinical supplies unit, TA strategy, regulatory affairs, data management,medical writing, biostatistics, global medical affairs, clinical pharmacology, clinical operations, health economics, epidemiology and other scientific and business related disciplines. The Project Physician may be asked to contribute to the evaluation of scientific opportunities in the therapeutic area Essential Functions: Responsible for medical monitoring/reporting and company safety officer activitiesWorks on clinical development plans, trial protocols and takes ownership of clinical study reportsEvaluates adverse events (pre and post-marketing) for relationship to treatmentAssists Regulatory Affairs in determining requirements for any corrective actions or health authority reportingMay act as a medical contact at the company for health authorities concerning clinical/medical issuesInterprets, reports and prepares oral and written results of product research, in concert with senior clinical personnel, in preparation for health authority submissionsClose interactions with Project Scientists and Physicians across programs Other Responsibilities : Assists Regulatory Affairs in the development of drug regulatory strategiesHelps explore and evaluate new product ideas to assist in identifying new market opportunitiesSupport general Clinical/Medical Affairs activities involving product evaluation, labeling and surveillanceParticipate on and may lead cross-functional teams for evaluation of new product ideas, implement franchise business strategies, etc.Reviews medical literature and related new technologiesMay be asked to assess medical publications emerging from the Team and its affiliatesMay be responsible, with appropriate colleagues, for review of Company advertising and promotional materials Candidate Profile: MD (or equivalent) in relevant area with appropriate post-doctoral training and certificationExperience and knowledge of Good Clinical Practices and regulatory requirements for the conduct of clinical trials and for the appropriate contributions to regulatory filingsSpecific experience in phase II and III studies is a strong advantage.Submission experience a strong advantage.Experience in medical review.Ideally previous experience in the Pulmonary Hypertension Therapeutic Area, otherwise Cardiovascular/Cardiopulmonary experience is appreciated.English Fluent Do not waste any minutes, apply now!  We are looking forward to receiving your application.Please note that only candidates with a valid work permit or who are EU/EFTA citizens will be considered.
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden - suchen wir genau dich per sofort oder nach Vereinbarung - einen qualifizierten Sanitärinstallateur EFZ (m/w/d) Deine AufgabenDu bist für die Beratung und Bedienung der Kunden verantwortlichKontrolle des Wareneingangs Unterstützung bei Materialbeschaffung, Ausmass und KoordinationArbeiten nach Skizzen und BauplänenErfassen von Lieferscheine mittels EDV System ( SAP )
    Exklusiv für unseren Kunden - suchen wir genau dich per sofort oder nach Vereinbarung - einen qualifizierten Sanitärinstallateur EFZ (m/w/d) Deine AufgabenDu bist für die Beratung und Bedienung der Kunden verantwortlichKontrolle des Wareneingangs Unterstützung bei Materialbeschaffung, Ausmass und KoordinationArbeiten nach Skizzen und BauplänenErfassen von Lieferscheine mittels EDV System ( SAP )
    • basel, basel-stadt
    • temporary
    Bezeichnest Du Dich als eine/n Steuerfachspezielisten/in und bist interessiert, unseren Kunden für einen befristeten Zeitraum mit Deinen Kenntnissen und Erfahrungen zu unterstützen? Dann suche ich genau Dich alsFachspezialist Steuern 100% (m/w/d)Dein Aufgabenbereich:Erstellung von SteuerunterlagenKorrekte und fristgerechte Abgabe von EinkommenssteuererklärungenVorbereitung von Steuerzahlungen und Verlängerungen Berechnung, Validierung und Einreichung von Steuererklärungen Durchführen von Abstimmungen für die QuartalsendprüfungBeantwortung verschiedener Anfragen der staatlichen SteuerbehördenUnterstützung bei der Konzernsteuerplanung/-vorhersage, der Cashflow-Planung und der monatlichen SteuerberechnungVerfolgung der Steuerpositionen in der Bilanz und der Gewinn- und Verlustrechnung im Laufe des Jahres und Abgleich mit Cash-Flow-Prognosen/Planung
    Bezeichnest Du Dich als eine/n Steuerfachspezielisten/in und bist interessiert, unseren Kunden für einen befristeten Zeitraum mit Deinen Kenntnissen und Erfahrungen zu unterstützen? Dann suche ich genau Dich alsFachspezialist Steuern 100% (m/w/d)Dein Aufgabenbereich:Erstellung von SteuerunterlagenKorrekte und fristgerechte Abgabe von EinkommenssteuererklärungenVorbereitung von Steuerzahlungen und Verlängerungen Berechnung, Validierung und Einreichung von Steuererklärungen Durchführen von Abstimmungen für die QuartalsendprüfungBeantwortung verschiedener Anfragen der staatlichen SteuerbehördenUnterstützung bei der Konzernsteuerplanung/-vorhersage, der Cashflow-Planung und der monatlichen SteuerberechnungVerfolgung der Steuerpositionen in der Bilanz und der Gewinn- und Verlustrechnung im Laufe des Jahres und Abgleich mit Cash-Flow-Prognosen/Planung
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Laborant (m/w/d) 100%In dieser Position bist Du zuständig für die Durchführung praktischer Arbeiten im Labor zur Qualifizierung von Referenzstandards (HPLC, NMR, Titrationen, IR, MS, Restlösungsmittelbestimmungen etc.)Du dokumentierst GMP-konform die durchgeführten Arbeiten im LIMS sowie die Auswertung der resultierenden RohdatenDu hilfst mit bei der Erstellung von Protokollen, Berichten und AnalysenzertifikatenDu unterstützt bei der Verwaltung von Referenzstandards (Ausgabe der Standards, Überwachung von Ablaufdaten und Restmengen)Du hilfst mit bei Qualifizierungen, Kalibrierungen und Wartungen der analytischen LaborgeräteDein Tätigkeitsgebiet wird abgerundet durch Deine Unterstützung bei der Erstellung von Vorgabedokumenten (SOP's) und Analysenvorschriften
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Laborant (m/w/d) 100%In dieser Position bist Du zuständig für die Durchführung praktischer Arbeiten im Labor zur Qualifizierung von Referenzstandards (HPLC, NMR, Titrationen, IR, MS, Restlösungsmittelbestimmungen etc.)Du dokumentierst GMP-konform die durchgeführten Arbeiten im LIMS sowie die Auswertung der resultierenden RohdatenDu hilfst mit bei der Erstellung von Protokollen, Berichten und AnalysenzertifikatenDu unterstützt bei der Verwaltung von Referenzstandards (Ausgabe der Standards, Überwachung von Ablaufdaten und Restmengen)Du hilfst mit bei Qualifizierungen, Kalibrierungen und Wartungen der analytischen LaborgeräteDein Tätigkeitsgebiet wird abgerundet durch Deine Unterstützung bei der Erstellung von Vorgabedokumenten (SOP's) und Analysenvorschriften
    • basel, basel-stadt
    • temp to perm
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Chemielaborant (m/w/d) 100%Herstellung von sterilen und nicht sterilen halbfesten und flüssigen ArzneiformenVor- und Nachbereitung der Herstellung (wie Sterilisations- und Reinigungsprozesse)Bedienen der ProduktionsanlagenProtokollieren der durchgeführten Arbeiten in der ProduktionsdokumentationArbeiten unter GMP Bedingungen
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Chemielaborant (m/w/d) 100%Herstellung von sterilen und nicht sterilen halbfesten und flüssigen ArzneiformenVor- und Nachbereitung der Herstellung (wie Sterilisations- und Reinigungsprozesse)Bedienen der ProduktionsanlagenProtokollieren der durchgeführten Arbeiten in der ProduktionsdokumentationArbeiten unter GMP Bedingungen
    • basel, basel-stadt
    • temp to perm
    Für unseren Kunden im Baselbiet suchen wir genau dich Operator Utilities / Instandhaltungsfachmann (m/w/d)Deine Hauptaufgaben:Sicherstellung von Betrieb, Unterhalt und Störungsbehebung an VersorgungsanlagenAusführen von Unterhaltsarbeiten, Revisionsarbeiten Behebung von Störungen an wichtigen technischen Anlagen mit hoher Priorität Protokoll über die durchgeführten Kontroll- und UnterhaltsarbeitenUnterstützung bei Audit und InspektionsanforderungenUnterstützung bei der Erstellung und / oder Support von Notice of Events (NOE), CAPAs, Abweichungen sowie Charge ControlsSchichtdienst 24h Betrieb
    Für unseren Kunden im Baselbiet suchen wir genau dich Operator Utilities / Instandhaltungsfachmann (m/w/d)Deine Hauptaufgaben:Sicherstellung von Betrieb, Unterhalt und Störungsbehebung an VersorgungsanlagenAusführen von Unterhaltsarbeiten, Revisionsarbeiten Behebung von Störungen an wichtigen technischen Anlagen mit hoher Priorität Protokoll über die durchgeführten Kontroll- und UnterhaltsarbeitenUnterstützung bei Audit und InspektionsanforderungenUnterstützung bei der Erstellung und / oder Support von Notice of Events (NOE), CAPAs, Abweichungen sowie Charge ControlsSchichtdienst 24h Betrieb
    • basel, basel-stadt
    • permanent
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen motivierten Automobil-MechatronikerDeine Aufgaben:Service-,Reparatur-Diagnose-Arbeiten führst du nach Hersteller-Richtlinien gewissenhaft durch.Selbständige Überprüfung des Unterhaltes im Tram. Dabei erkennst du mögliche Störungen und behebst diese Sorgfältig.Du leistest einen hohen Beitrag zur Kundenzufriedenheit
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen motivierten Automobil-MechatronikerDeine Aufgaben:Service-,Reparatur-Diagnose-Arbeiten führst du nach Hersteller-Richtlinien gewissenhaft durch.Selbständige Überprüfung des Unterhaltes im Tram. Dabei erkennst du mögliche Störungen und behebst diese Sorgfältig.Du leistest einen hohen Beitrag zur Kundenzufriedenheit
    • basel, basel-stadt
    • temp to perm
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Polymechaniker EFZ (m/w)Deine Aufgaben:Verantwortung für Service, Reparatur und Wartung Ansprechpartner bei technischen Problemen Organisation und Unterstützung externer Firmen Unterstützung bei Um-und Neubaumassnahmen Umsetzung von technischen Optimierungen Nachführen von technischen Unterlagen
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Polymechaniker EFZ (m/w)Deine Aufgaben:Verantwortung für Service, Reparatur und Wartung Ansprechpartner bei technischen Problemen Organisation und Unterstützung externer Firmen Unterstützung bei Um-und Neubaumassnahmen Umsetzung von technischen Optimierungen Nachführen von technischen Unterlagen
    • basel, basel-stadt
    • temp to perm
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Betriebselektriker oder Automatiker. (m/w)Deine Aufgaben:Störungsanalyse, Fehlerbehebung und Reparatur an Produktionsanlagen und InfrastrukturUmsetzung von technischen Optimierungen (Steuerung- , Regel und Antriebstechnik)Projektmitarbeit bei Umbauten, Neuinstallationen und Inbetriebnahmen von Maschinen und AnlagenNachführen von technischen Unterlagen und Schemas
    Für die Region Basel suchen wir per sofort oder nach Vereinbarung einen hoch motivierten Betriebselektriker oder Automatiker. (m/w)Deine Aufgaben:Störungsanalyse, Fehlerbehebung und Reparatur an Produktionsanlagen und InfrastrukturUmsetzung von technischen Optimierungen (Steuerung- , Regel und Antriebstechnik)Projektmitarbeit bei Umbauten, Neuinstallationen und Inbetriebnahmen von Maschinen und AnlagenNachführen von technischen Unterlagen und Schemas
    • basel, basel-stadt
    • permanent
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Rohschlosser (m/w/d) 100%Deine AufgabenEntwicklung und Fertigung von Rohrleitungen und Anlagen Verarbeiten von Stahl- & Edelstahlrohren Diverse Schweiß-Arbeiten
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Rohschlosser (m/w/d) 100%Deine AufgabenEntwicklung und Fertigung von Rohrleitungen und Anlagen Verarbeiten von Stahl- & Edelstahlrohren Diverse Schweiß-Arbeiten
    • basel, basel-stadt
    • permanent
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Maurer (m/w/d) 100%Erstellen von MauerwerkenAllgemeine Schalungsarbeiten wie Doka, Peri SchalungenMess- und Nivellierarbeiten BetonierenVerputzarbeiten
    Exklusiv für unseren Kunden im Raum Basel , suchen wir genau Dich ein Motivierten Maurer (m/w/d) 100%Erstellen von MauerwerkenAllgemeine Schalungsarbeiten wie Doka, Peri SchalungenMess- und Nivellierarbeiten BetonierenVerputzarbeiten
    • basel, basel-stadt
    • permanent
    Für unseren Kunden im Raum Basel suchen wir genau dich ab sofort oder nach Vereinbarung einen:Kältetechniker (m/w/d)Deine Hauptaufgaben:Instandhaltung und Umbau von kältetechnischen Anlagen und SystemenStörungsbehebungen an kältetechnischen AnlagenDurchführung der periodischen WartungenPlanung, Kontrolle und Ausführung aller notwendigen Arbeiten in Zusammenarbeit mit den zuständigen internen und kundenseitigen StellenErstellen der notwendigen Dokumentationen, Rapporte etc.Leisten von Pikettdienst
    Für unseren Kunden im Raum Basel suchen wir genau dich ab sofort oder nach Vereinbarung einen:Kältetechniker (m/w/d)Deine Hauptaufgaben:Instandhaltung und Umbau von kältetechnischen Anlagen und SystemenStörungsbehebungen an kältetechnischen AnlagenDurchführung der periodischen WartungenPlanung, Kontrolle und Ausführung aller notwendigen Arbeiten in Zusammenarbeit mit den zuständigen internen und kundenseitigen StellenErstellen der notwendigen Dokumentationen, Rapporte etc.Leisten von Pikettdienst
    • basel, basel-stadt
    • permanent
    Exklusiv für unseren Kunden, ein international erfolgreiches Unternehmen, suchen wir genau DichMetallbauer/ EFZSelbständiges ArbeitenAllgemeine Schlosserarbeiten Schweißen Durchführung der Qualitätskontrolle
    Exklusiv für unseren Kunden, ein international erfolgreiches Unternehmen, suchen wir genau DichMetallbauer/ EFZSelbständiges ArbeitenAllgemeine Schlosserarbeiten Schweißen Durchführung der Qualitätskontrolle
    • basel, basel-stadt
    • permanent
    Dein Aufgabenbereich• Die Betreuung der Kundenanliegen und eine rasche Umsetzung des Sollzustandes.• Eine proaktive und saubere Kommunikation mit dem Kunden und Vorgesetzten• Das selbstständige Beheben von Mängel unter Einbezug der Internen und externen Lieferanten• Die Mithilfe bei Rundgängen, Inspektionen und Wartungsarbeiten• Die Koordination der Instandsetzung von Geräten in Produktions- und Bürogebäuden• Einholen von Offerten für Dienstleistungen und Waren bei Intern und Externen Lieferanten
    Dein Aufgabenbereich• Die Betreuung der Kundenanliegen und eine rasche Umsetzung des Sollzustandes.• Eine proaktive und saubere Kommunikation mit dem Kunden und Vorgesetzten• Das selbstständige Beheben von Mängel unter Einbezug der Internen und externen Lieferanten• Die Mithilfe bei Rundgängen, Inspektionen und Wartungsarbeiten• Die Koordination der Instandsetzung von Geräten in Produktions- und Bürogebäuden• Einholen von Offerten für Dienstleistungen und Waren bei Intern und Externen Lieferanten
    • basel, basel-stadt
    • temporary
    Für unseren Kunden suchen wir top motivierte/n Maler/in mit EFZDeine AufgabenAbdecken/Abkleben Arbeitsflächen Grundierungsarbeiten und Spachtelarbeiten Einsatz im Neu-, Umbau- und Renovation Streichen von: Fassaden/ Fenster/ Türen/Holz/ Metall/ Kunststoff Tapezieren/ Kleistern/ Kleben/ Aufziehen
    Für unseren Kunden suchen wir top motivierte/n Maler/in mit EFZDeine AufgabenAbdecken/Abkleben Arbeitsflächen Grundierungsarbeiten und Spachtelarbeiten Einsatz im Neu-, Umbau- und Renovation Streichen von: Fassaden/ Fenster/ Türen/Holz/ Metall/ Kunststoff Tapezieren/ Kleistern/ Kleben/ Aufziehen
    • basel, basel-stadt
    • temp to perm
    Betriebselektriker (w/m)Ihre AufgabenWartungen und Instandhaltungen an elektrischen Anlagen Erstellen von technischen Dokumenten Störungsanalyse und Störungsbehebung Beaufsichtigen von Fremdfirmen Unterstützung der Inbetriebnahme von Automationsanlagen Stetige Weiterbildung im Aufgabenbereich
    Betriebselektriker (w/m)Ihre AufgabenWartungen und Instandhaltungen an elektrischen Anlagen Erstellen von technischen Dokumenten Störungsanalyse und Störungsbehebung Beaufsichtigen von Fremdfirmen Unterstützung der Inbetriebnahme von Automationsanlagen Stetige Weiterbildung im Aufgabenbereich
    • basel, basel-stadt
    • contract
    Randstad Professionals is looking for an Associate Director, Signal Management for a major client. This position will be based in Basel .Startdate: ASAP (up to 3 month notice period possible)Contract: 12 monthsThis position will have a high degree of visibility and impact across the organization and will collaborate closely cross-functionally and cross-regionally. Your responsibilities:Provide dynamic strategic contribution to the direction and senior leaders of key pharmacovigilance activities across portfolio and throughout the clinical development and post-marketing phases of the life cycle including: Lead all signal management activities for assigned product(s)  Support implantation of signal detection strategy approved by VP of Pharmacovigilance  Review adverse event data, literature and other safety-related data for the purpose of signal detection  Collaborate with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues to review safety data for signal validation, prioritization, assessment and proposed action plans Partner with the Director, Pharmacovigilance – Signal Management to oversee digital signal detection and management tool.  Serve as an administrator of the tool  Propose and implement signal detection methods in the tool  Train, mentor and assist CSRM staff in using the tool.  Oversee signal tracking and signal notifications to external stakeholders  Generate periodic signal management compliance metrics Provide safety contents for risk management plans and periodic aggregate safety reports, including but not limited to PBRER/PSUR, PADER, DSUR, and IND annual reports in collaboration with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues Assess document requirements, gauge document complexity, and identify information gaps or other potential issues. In collaboration with the relevant project team, the author proposes or contributes to strategies to resolve any identified issues  Reviews applicable regulatory intelligence on global regulations/guidance documents and be able to advise report project teams as a Subject Matter Expert (SME) for signal management.  Understand relationships and dependencies between signal management and documents/analyses produced for regulators across the development of RMPs, DSURs, PBRERs, and other annual reports and/or deliverables  Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission  Provide project teams with expertise and strategic guidance on analysis and presentation of safety data and on benefit-risk assessment in documents  Produce high quality, accurate, and fit-for-purpose evaluation documents with clear conclusions, in response to internal or regulatory authority request for safety reasons  Review the worldwide medical/scientific literature to identify signals and applicable information for inclusion in aggregate safety reports in collaboration with CSRM colleagues  Draft regulatory response documents such as PRAC assessment reports  Draft other medical writing deliverables as needed If you are interested to take on these responsibilities you should have the following requirements:Degree in Pharmacy, Nursing, Epidemiology, Biosciences or equivalent healthcare degree with pharmaceutical industry background  Minimum 8 years relevant medical, scientific/clinical, or pharmaceutical experience, including at least 5 years’ experience in Pharmacovigilance  Excellent written and verbal communication skills with the ability to interpret and present safety data  Knowledge of FDA and EMA regulations, ICH guidelines, Good Clinical Practices, and the drug development process  Knowledge of drug safety/pharmacovigilance practices and tools  Ability to coordinate and prioritize multiple projects in a fast-paced environment with limited to little supervision  Background in vaccines is a plus  Demonstrated ability to develop, execute and follow-through complex projects to completion  Skilled at working effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view  Independently motivated, detail oriented and strong problem-solving ability  Excellent organizational skills and demonstrated ability to multitask in a fast-paced environment with changing priorities  Excellent written and verbal communication skills with the ability to interact across multiple functions Did we spark your interest? We look forward to receiving your online application. Please note a Swiss Work permit is mandatory and your residence needs to be in Switzerland for this position. 
    Randstad Professionals is looking for an Associate Director, Signal Management for a major client. This position will be based in Basel .Startdate: ASAP (up to 3 month notice period possible)Contract: 12 monthsThis position will have a high degree of visibility and impact across the organization and will collaborate closely cross-functionally and cross-regionally. Your responsibilities:Provide dynamic strategic contribution to the direction and senior leaders of key pharmacovigilance activities across portfolio and throughout the clinical development and post-marketing phases of the life cycle including: Lead all signal management activities for assigned product(s)  Support implantation of signal detection strategy approved by VP of Pharmacovigilance  Review adverse event data, literature and other safety-related data for the purpose of signal detection  Collaborate with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues to review safety data for signal validation, prioritization, assessment and proposed action plans Partner with the Director, Pharmacovigilance – Signal Management to oversee digital signal detection and management tool.  Serve as an administrator of the tool  Propose and implement signal detection methods in the tool  Train, mentor and assist CSRM staff in using the tool.  Oversee signal tracking and signal notifications to external stakeholders  Generate periodic signal management compliance metrics Provide safety contents for risk management plans and periodic aggregate safety reports, including but not limited to PBRER/PSUR, PADER, DSUR, and IND annual reports in collaboration with Clinical Safety and Risk Management (CSRM) physicians, safety scientists, and medical colleagues Assess document requirements, gauge document complexity, and identify information gaps or other potential issues. In collaboration with the relevant project team, the author proposes or contributes to strategies to resolve any identified issues  Reviews applicable regulatory intelligence on global regulations/guidance documents and be able to advise report project teams as a Subject Matter Expert (SME) for signal management.  Understand relationships and dependencies between signal management and documents/analyses produced for regulators across the development of RMPs, DSURs, PBRERs, and other annual reports and/or deliverables  Provide project teams with expertise on regulatory requirements and corporate policies governing documents for regulatory submission  Provide project teams with expertise and strategic guidance on analysis and presentation of safety data and on benefit-risk assessment in documents  Produce high quality, accurate, and fit-for-purpose evaluation documents with clear conclusions, in response to internal or regulatory authority request for safety reasons  Review the worldwide medical/scientific literature to identify signals and applicable information for inclusion in aggregate safety reports in collaboration with CSRM colleagues  Draft regulatory response documents such as PRAC assessment reports  Draft other medical writing deliverables as needed If you are interested to take on these responsibilities you should have the following requirements:Degree in Pharmacy, Nursing, Epidemiology, Biosciences or equivalent healthcare degree with pharmaceutical industry background  Minimum 8 years relevant medical, scientific/clinical, or pharmaceutical experience, including at least 5 years’ experience in Pharmacovigilance  Excellent written and verbal communication skills with the ability to interpret and present safety data  Knowledge of FDA and EMA regulations, ICH guidelines, Good Clinical Practices, and the drug development process  Knowledge of drug safety/pharmacovigilance practices and tools  Ability to coordinate and prioritize multiple projects in a fast-paced environment with limited to little supervision  Background in vaccines is a plus  Demonstrated ability to develop, execute and follow-through complex projects to completion  Skilled at working effectively in a collaborative team environment where results are achieved through influence and the incorporation of multiple points of view  Independently motivated, detail oriented and strong problem-solving ability  Excellent organizational skills and demonstrated ability to multitask in a fast-paced environment with changing priorities  Excellent written and verbal communication skills with the ability to interact across multiple functions Did we spark your interest? We look forward to receiving your online application. Please note a Swiss Work permit is mandatory and your residence needs to be in Switzerland for this position. 
    • basel, basel-stadt
    • temporary
    Do you have good communication skills and strong experience in the bio-pharmaceutical industry?Are you experienced working with partner organizations (CMOs)?In this case you should have a look at this opportunity!To work for our client, a pioneering biotechnology company, we are looking for a: Senior Specialist, International Fill FinishLocation: BaselContract duration: to start asap for 12 monthsHere’s What You’ll Do: Support the (Associate) Director, International Fill Finish in various tasks related to the buildup of GMP production at Fill Finish Contract Manufacturing Organizations (FF CMOs). Act as a counterpart for FF CMOs team members to ensure on-time and in-full deliveries. Partner with Quality, Technical Development, Manufacturing Science and Technology, and Regulatory colleagues on specific aspects of the relationships with the FF CMOs.Ensure operational related activities at the FF CMOs are conducted to meet Company’s requirements (Compliance, Meeting Orders, Dispute resolution, Production Planning, Materials Management, Technology Issues, OpEx). Ensure externally manufactured drug products are produced and stored according to the appropriate documentation in order to obtain the required quality. Ensure that instructions relating to external production operations are strictly implemented by the  CMOs.Ensure in collaboration with quality that the appropriate qualification, maintenance, training and validations are performed to meet the appropriate Company requirements. Support and perform the reviews for process performance at FF CMOs. Monitor Key Performance Indicators of FF CMOs. Support preparation of periodic business and operations review meetings.  Drive for and implement agreed continuous improvements at FF CMOs. Coordinate reviews and approvals of various documentations from FF CMOs. In collaboration with Quality coordinate investigations and troubleshooting efforts at FF CMOsWrite or revise the appropriate GMP documentations. Frequently visit and maintain presence at the external partners’ sites and build strong interdependent relationships with the CMO Counterparts in order to assess the as is state & risks for action-oriented improvement plans. Performs other administrative duties as required. Here’s What You’ll Bring to the Table:Bachelor's Degree with 5-8 years of experience in biopharmaceutical operations or a Master’s Degree with 2-5 years industry experience; Degree in Engineering or Life Sciences is preferred.Proficiency in English required. Spanish and German are a plus. Good communication skills (verbal and written) to collaborate with other CMC team members and managers in a dynamic, cross-functional matrix environment.Ability to work with members of partner organizations (CMOs).Well organized – a natural ability to be organized in how you think, communicate and conduct your work.You drive for results – you set a high bar for yourself and others.Good critical thinker that can anticipate the needed next step and therefore can work independently.A curious mindset that allows you to constantly learn and challenge the status quo.Ability to navigate through ambiguity and rapid growth and adapt to change.  You would like to contribute to a fast-thinking and innovative company, changing the industry ?Apply now! Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    Do you have good communication skills and strong experience in the bio-pharmaceutical industry?Are you experienced working with partner organizations (CMOs)?In this case you should have a look at this opportunity!To work for our client, a pioneering biotechnology company, we are looking for a: Senior Specialist, International Fill FinishLocation: BaselContract duration: to start asap for 12 monthsHere’s What You’ll Do: Support the (Associate) Director, International Fill Finish in various tasks related to the buildup of GMP production at Fill Finish Contract Manufacturing Organizations (FF CMOs). Act as a counterpart for FF CMOs team members to ensure on-time and in-full deliveries. Partner with Quality, Technical Development, Manufacturing Science and Technology, and Regulatory colleagues on specific aspects of the relationships with the FF CMOs.Ensure operational related activities at the FF CMOs are conducted to meet Company’s requirements (Compliance, Meeting Orders, Dispute resolution, Production Planning, Materials Management, Technology Issues, OpEx). Ensure externally manufactured drug products are produced and stored according to the appropriate documentation in order to obtain the required quality. Ensure that instructions relating to external production operations are strictly implemented by the  CMOs.Ensure in collaboration with quality that the appropriate qualification, maintenance, training and validations are performed to meet the appropriate Company requirements. Support and perform the reviews for process performance at FF CMOs. Monitor Key Performance Indicators of FF CMOs. Support preparation of periodic business and operations review meetings.  Drive for and implement agreed continuous improvements at FF CMOs. Coordinate reviews and approvals of various documentations from FF CMOs. In collaboration with Quality coordinate investigations and troubleshooting efforts at FF CMOsWrite or revise the appropriate GMP documentations. Frequently visit and maintain presence at the external partners’ sites and build strong interdependent relationships with the CMO Counterparts in order to assess the as is state & risks for action-oriented improvement plans. Performs other administrative duties as required. Here’s What You’ll Bring to the Table:Bachelor's Degree with 5-8 years of experience in biopharmaceutical operations or a Master’s Degree with 2-5 years industry experience; Degree in Engineering or Life Sciences is preferred.Proficiency in English required. Spanish and German are a plus. Good communication skills (verbal and written) to collaborate with other CMC team members and managers in a dynamic, cross-functional matrix environment.Ability to work with members of partner organizations (CMOs).Well organized – a natural ability to be organized in how you think, communicate and conduct your work.You drive for results – you set a high bar for yourself and others.Good critical thinker that can anticipate the needed next step and therefore can work independently.A curious mindset that allows you to constantly learn and challenge the status quo.Ability to navigate through ambiguity and rapid growth and adapt to change.  You would like to contribute to a fast-thinking and innovative company, changing the industry ?Apply now! Please note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    • basel, basel-stadt
    • temporary
    Do you wish to be part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative ?For our client, this pioneering biotechnology company, we are looking for a: Senior Associate, International Manufacturing Operations Location:BaselContract: Temporary for one year. This role is an exciting opportunity to be part of a growing Supply Chain/Manufacturing group. Reporting to Director of International Manufacturing, the successful candidate will work closely with the CMO manufacturing function and Supply Chain function to ensure that the SAP operations are accurate, on track, and in line with GMP compliance and regulatory requirements.Your Responsibilities: Weekly open order book management in collaboration with Manufacturing/Supply Chain in the CMO. The objective is to ensure that the CMO is on track to deliver all released process orders, on-time and in-full. Risks, Opportunities and Issues should be raised and resolved daily.  Daily, or Weekly, Toll material reconciliation process to ensure: All usage of company-owned toll manufacturing materials, by the CMO, is reconciled and accounted for, and that investigations are performed when reconciliation results are outside pre-defined thresholds. That material usage, and inventory transactions, at the CMO are accurately reflected in the SAP system, in a timely way. This can be achieved either through company/CMO system interfaces, or through a manual toll-reconciliation process owned by the Planner.  Execute good receipt and inventory movement transactions required to ensure cross system inventory placement / inventory accuracy Execute the regular raw materials booking within the open process orders in line with CMOs information.Executed Process Orders TECO once that the process orders operations are completed  Ensure compliance with GMP and regulatory requirements (including records management) and spearheads continuous improvements for quality financial flow processes. Your profile:Bachelor level degree in Supply Chain, Business or related field  Between 2 and 3 years of experience in the manufacturing Site preferably as Batch Record Reviewer  Experience in Operation of a highly regulated industry, like Pharmaceutical or related field.  Experience executing SAP Process Orders Raw Materials consumption/Booking .  Ability to manage multiple topics in a fast-paced environment and deal with different stakeholders from different domains in the organization.  Demonstrated ability to critically think and identify solutions.  Well organized – a natural ability to be organized in how you think, communicate and conduct your work  A curious mindset that allows you to constantly learn and challenge the status quo You would like to contribute to a fast-thinking and innovative company, changing the industry ? Apply nowPlease note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    Do you wish to be part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative ?For our client, this pioneering biotechnology company, we are looking for a: Senior Associate, International Manufacturing Operations Location:BaselContract: Temporary for one year. This role is an exciting opportunity to be part of a growing Supply Chain/Manufacturing group. Reporting to Director of International Manufacturing, the successful candidate will work closely with the CMO manufacturing function and Supply Chain function to ensure that the SAP operations are accurate, on track, and in line with GMP compliance and regulatory requirements.Your Responsibilities: Weekly open order book management in collaboration with Manufacturing/Supply Chain in the CMO. The objective is to ensure that the CMO is on track to deliver all released process orders, on-time and in-full. Risks, Opportunities and Issues should be raised and resolved daily.  Daily, or Weekly, Toll material reconciliation process to ensure: All usage of company-owned toll manufacturing materials, by the CMO, is reconciled and accounted for, and that investigations are performed when reconciliation results are outside pre-defined thresholds. That material usage, and inventory transactions, at the CMO are accurately reflected in the SAP system, in a timely way. This can be achieved either through company/CMO system interfaces, or through a manual toll-reconciliation process owned by the Planner.  Execute good receipt and inventory movement transactions required to ensure cross system inventory placement / inventory accuracy Execute the regular raw materials booking within the open process orders in line with CMOs information.Executed Process Orders TECO once that the process orders operations are completed  Ensure compliance with GMP and regulatory requirements (including records management) and spearheads continuous improvements for quality financial flow processes. Your profile:Bachelor level degree in Supply Chain, Business or related field  Between 2 and 3 years of experience in the manufacturing Site preferably as Batch Record Reviewer  Experience in Operation of a highly regulated industry, like Pharmaceutical or related field.  Experience executing SAP Process Orders Raw Materials consumption/Booking .  Ability to manage multiple topics in a fast-paced environment and deal with different stakeholders from different domains in the organization.  Demonstrated ability to critically think and identify solutions.  Well organized – a natural ability to be organized in how you think, communicate and conduct your work  A curious mindset that allows you to constantly learn and challenge the status quo You would like to contribute to a fast-thinking and innovative company, changing the industry ? Apply nowPlease note that a valid Swiss work permit or Swiss or EU-25/EFTA citizenship is required for this position
    • basel, basel-stadt
    • contract
    Das Department Technische Compliance ist auf der Suche nach einem/r Compliance Experte (m/w/d) für die Betreuung & Implementierung von Qualitätssystemen innerhalb des Engineerings & Energiebetrieben/Werkstätten. Allgemeine Informationen: • Startdatum: asap• Spätestmögliches Startdatum: 01.11.2021• Enddatum: Jahresvertrag• Verlängerung: Wahrscheinlich• Workload: 80-100%• Home Office: nach Absprache zeitweise möglich  Aufgaben & Verantwortlichkeiten: • Unterstützung interner Kunden als anerkannter Berater in sämtlichen technischen GMP Fragestellungen, z.B. Umsetzung von Qualifizierungsanforderungen• Monitoring von Key Performance Indices und Fälligkeiten• Business Process Support für Risk-, Deviation-, Change- und CAPA-Management in enger Kollaboration mit den Qualitätsorganisationen am Standort• Inspektionssupport für den Bereich Technik, Kontakt zu den Subject Matter Experts• Unterstützung und aktive Mitarbeit in agilen Organisationsformen• Unterstützung im Records-Management Must Haves: • Abgeschlossenes technisches Studium oder vergleichbare Ausbildung mit langjähriger Berufserfahrung • Mind. 3 Jahre praktische Erfahrung im Bereich Compliance/Qualitätssicherung von pharmazeutischen, chemischen oder biotechnologischen Anlagen • Praktische Erfahrung in der Umsetzung von technischen GMP-Anforderungen der Zulassungsbehörden (RHI, FDA, EMA etc.) in Investitionsprojekten bzw. in der galenischen/chemischen Produktion• Gute EDV-Kenntnisse (GSuite), Erfahrung in TrackWise, Condor und Veeva von Vorteil• Sehr gute Deutsch- und Englisch- Kenntnisse in Wort und Schrift Persönliche Anforderungen: • Teamplayer mit exzellenten Kommunikationseigenschaften und Verhandlungsfähigkeiten, gepaart mit der Fähigkeit effektive und vertrauensvolle Beziehungen mit Kollegen und Mitarbeitern auf verschiedensten Ebenen aufzubauen• Eigenverantwortliche und selbständige Bearbeitung komplexer Aufgaben sowie zuverlässige Durchsetzung vereinbarter Prioritäten• offen für neue Ideen und hinterfragen konventionelle Denkmuster.
    Das Department Technische Compliance ist auf der Suche nach einem/r Compliance Experte (m/w/d) für die Betreuung & Implementierung von Qualitätssystemen innerhalb des Engineerings & Energiebetrieben/Werkstätten. Allgemeine Informationen: • Startdatum: asap• Spätestmögliches Startdatum: 01.11.2021• Enddatum: Jahresvertrag• Verlängerung: Wahrscheinlich• Workload: 80-100%• Home Office: nach Absprache zeitweise möglich  Aufgaben & Verantwortlichkeiten: • Unterstützung interner Kunden als anerkannter Berater in sämtlichen technischen GMP Fragestellungen, z.B. Umsetzung von Qualifizierungsanforderungen• Monitoring von Key Performance Indices und Fälligkeiten• Business Process Support für Risk-, Deviation-, Change- und CAPA-Management in enger Kollaboration mit den Qualitätsorganisationen am Standort• Inspektionssupport für den Bereich Technik, Kontakt zu den Subject Matter Experts• Unterstützung und aktive Mitarbeit in agilen Organisationsformen• Unterstützung im Records-Management Must Haves: • Abgeschlossenes technisches Studium oder vergleichbare Ausbildung mit langjähriger Berufserfahrung • Mind. 3 Jahre praktische Erfahrung im Bereich Compliance/Qualitätssicherung von pharmazeutischen, chemischen oder biotechnologischen Anlagen • Praktische Erfahrung in der Umsetzung von technischen GMP-Anforderungen der Zulassungsbehörden (RHI, FDA, EMA etc.) in Investitionsprojekten bzw. in der galenischen/chemischen Produktion• Gute EDV-Kenntnisse (GSuite), Erfahrung in TrackWise, Condor und Veeva von Vorteil• Sehr gute Deutsch- und Englisch- Kenntnisse in Wort und Schrift Persönliche Anforderungen: • Teamplayer mit exzellenten Kommunikationseigenschaften und Verhandlungsfähigkeiten, gepaart mit der Fähigkeit effektive und vertrauensvolle Beziehungen mit Kollegen und Mitarbeitern auf verschiedensten Ebenen aufzubauen• Eigenverantwortliche und selbständige Bearbeitung komplexer Aufgaben sowie zuverlässige Durchsetzung vereinbarter Prioritäten• offen für neue Ideen und hinterfragen konventionelle Denkmuster.
    • basel, basel-stadt
    • contract
    Bist du ein motivierter Junior Validation Engineer und du bist auf der Suche nach einer Herausforderung?  Wichtige Details:  Temporär - JahresvertragStartdatum: asap Aufgaben und Verantwortlichkeiten: Verantwortlich für die Prozessvalidierung im Bereich der WirkstoffherstellungKonzeption, Planung und Koordination von ProzessvalidierungsprojektenUnterstützung aller Prozessvalidierungsaktivitäten (Planung, Sampling und Reporting) für die routinemässige Produktion sowie für neue Produktimplementierungen, Prozessvalidierung in Technical Transfer ProjektenDatenaufbereitung und -analyse; Erstellung z.B. von Dokumenten, Fliessschemata und technischen ZeichnungenStudien zu Extractables und Leachables (E/L)Unterstützung bei der Implementierung und Qualifizierung von direct materialsMitarbeit in globalen Netzwerkteams z.B. direct materials, ProzessvalidierungBearbeitung von Abweichungen und Changes gemäss GMP-Richtlinienkontinuierliche Prozessverbesserung Must Haves: Hochschulabschluss (oder gleichwertige Ausbildung/Erfahrung) in einem wissenschaftlichen oder technischen Fachgebiet - Vorzugsweise im Bereich Biotechnologie, Bioprozesstechnik, oder (Bio-)chemische VerfahrenstechnikMind. 1 Jahr Berufserfahrung in einem GMP-regulierten ArbeitsumfeldErste Erfahrung in der Planung und Durchführung von Prozessvalidierungs- oder Charakterisierungsstudien Erste Erfahrung in der Planung und Koordination sowie am Umgang mit Dokumenten Sehr gute Deutsch- und Englischkenntnisse werden vorausgesetztErfahrungen im Gebiet Single-Use Technologien sind von VorteilErfahrungen im Gebiet Prozesstransfers von sind VorteilFähigkeit sich einem schnell ändernden Umfeld mit wechselnden Prioritäten anzupassen und flexibel auf Anfragen zu reagierenSehr gute (auch interkulturelle) Kommunikationsfähigkeiten Ich freue mich auf deine Bewerbung!
    Bist du ein motivierter Junior Validation Engineer und du bist auf der Suche nach einer Herausforderung?  Wichtige Details:  Temporär - JahresvertragStartdatum: asap Aufgaben und Verantwortlichkeiten: Verantwortlich für die Prozessvalidierung im Bereich der WirkstoffherstellungKonzeption, Planung und Koordination von ProzessvalidierungsprojektenUnterstützung aller Prozessvalidierungsaktivitäten (Planung, Sampling und Reporting) für die routinemässige Produktion sowie für neue Produktimplementierungen, Prozessvalidierung in Technical Transfer ProjektenDatenaufbereitung und -analyse; Erstellung z.B. von Dokumenten, Fliessschemata und technischen ZeichnungenStudien zu Extractables und Leachables (E/L)Unterstützung bei der Implementierung und Qualifizierung von direct materialsMitarbeit in globalen Netzwerkteams z.B. direct materials, ProzessvalidierungBearbeitung von Abweichungen und Changes gemäss GMP-Richtlinienkontinuierliche Prozessverbesserung Must Haves: Hochschulabschluss (oder gleichwertige Ausbildung/Erfahrung) in einem wissenschaftlichen oder technischen Fachgebiet - Vorzugsweise im Bereich Biotechnologie, Bioprozesstechnik, oder (Bio-)chemische VerfahrenstechnikMind. 1 Jahr Berufserfahrung in einem GMP-regulierten ArbeitsumfeldErste Erfahrung in der Planung und Durchführung von Prozessvalidierungs- oder Charakterisierungsstudien Erste Erfahrung in der Planung und Koordination sowie am Umgang mit Dokumenten Sehr gute Deutsch- und Englischkenntnisse werden vorausgesetztErfahrungen im Gebiet Single-Use Technologien sind von VorteilErfahrungen im Gebiet Prozesstransfers von sind VorteilFähigkeit sich einem schnell ändernden Umfeld mit wechselnden Prioritäten anzupassen und flexibel auf Anfragen zu reagierenSehr gute (auch interkulturelle) Kommunikationsfähigkeiten Ich freue mich auf deine Bewerbung!
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