2676 jobs found for Pharmaceutical

about the company:My client is a premier provider of cutting-edge scientific and medical solutions, specializing in laboratory equipment, reagents, and top-tier consulting services Location: TuasWork Schedule: Monday to Friday, Officer hours Job scope:Lead warehousing and supply chain teams in managing inventory, warehouse operations, and supply chain improvements.Plan, coordinate, and execute all warehouse operations, including secondary assemblies and tr

Our client is a prestigious pharmaceutical company that aims to recruit a Qualified Person.

Are you an experienced Senior Scientist? Do you have experience in sterile drug product development / manufacturing within the pharmaceutical industry? We are recruiting for a Senior Scientist to work within Drug Product Development establishing robust, fit for purpose biologicals drug product manufacturing processes for the different development phases. You will be defining and selecting drug product manufacturing processes and parameters for clinical man

Do you consider yourself to be an organised individual, with great communication skills? Are you able to work effectively to provide procedural reports and updates? If so, we are looking for an individual who would be interested in joining a UK EHS Commercial Manager. You will be responsible for a number of tasks from supporting issues or incidents, conducting reviews and chairing committee meetings.Role details:Title - UK EHS Commercial ManagerLocation -

社名社名非公開職種薬事、メディカルライティング業務内容• Serving as a contact point for the company, coordinates for pharmaceutical affairs matters on product development between internal concerned departments and regulatory authority.• Performs pharmaceutical regulatory affairs tasks for obtaining pharmaceutical product approval.• Prepares various pharmaceutical regulatory affairs documents in a timely and appropriate manner according to the product development plan.• Manages pharma

One of our leading private healthcare clients are looking for a dynamic Procurement Manager to join their pathology team! With specific and high level laboratory experience the Procurement Manager will ensure best in class industry pricing and contract terms and conditions, whilst managing a small team to support our key stakeholder with the procurement of outsourced pathology services.Essential Experience required to be considered:*Laboratory Procurement

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working

Become part of our innovative team at Waltham and contribute to scientific breakthroughs that improve the lives of millions of pets worldwide. As a Bioscience Laboratory Scientist, you will execute a range of experimental techniques and methodologies with precision and technical expertise to advance research projects.Key Responsibilities:Execute various laboratory methodologies to generate high-quality data aligned with project objectives set by Senior Res

Are you looking to join a dynamic team as an Administrative Assistant in the pharmaceutical industry? Are you a motivated Administrative Assistant supporting marketing department for the past 1-2 years? If you're a passionate professional and eager to continue making a difference in the pharmaceutical industry on a fixed term contract, we want to hear from you! Apply now to embark on a rewarding career journey!!

社名社名非公開職種法務、コンプライアンス、内部統制業務内容**Job Title: Pharma Counsel****Company:** International Pharmaceutical Company**Location:** Tokyo, Japan**About My Client:**My client is a leading international pharmaceutical company with a strong commitment to improving global healthcare through innovative research, development, and distribution of pharmaceutical products. My client's mission is to make a positive impact on the lives of people around the world by delivering h

Are you an experienced Senior Scientist? Do you have experience in recombinant protein production? We are recruiting for a Senior Scientist to work within our clients Protein Production Group supporting projects from early stage target validation through to those undergoing pre-clinical evaluation, by generating recombinant protein reagents for immunisation, structural studies, assays and compound screening. All reagents produced undergo biophysical analys

Do you consider yourself to be strong at relationship and stakeholder management, with great communication skills? Are you able to work effectively, implementing procurement strategies that will deliver best value for the business? If so, we are looking for an individual who would be interested in joining a global medical device manufacturer as a supplier account manager. You will be responsible for a number of tasks from negotiation of commercial contrac

Are you an experienced Labelling Lead? Do you have pharmaceutical or biotechnology regulatory experience, including regulatory labelling? If so, our Biotechnology client is looking for individuals just like you! The purpose of the Global Labelling group is to drive the core labelling strategy and ensure that labelling documents are of high quality and compliant for the safe and effective use of our clients products for patients and healthcare providers glo

Are you interested in working in a Laboratory environment? Do you have the ability to follow instructions and processes? We are recruiting for a Lab Assistant to support our clients team in the laboratory carrying our routine tasks required to keep the lab running smoothly! Our client is offering full training, a lab background is not required. We welcome applications from all backgrounds if you have the ability to learn! The successful candidate will be

Project Coordinator Location: Slough Full Time: 37.5 hours Weekly, 7.5 hours Daily Contract: 6 months, possible extension Salary: £17.02 PAYE Are you driven to succeed? Dependable, and a trouble shooter? Do you have the ability to build excellent relationships, manage projects and finances? If so, we want you to consider becoming part of a Global business leader in our industry; helping us drive our businesses growth by assisting with our upcoming proje

Position: Clinical Data AdministratorLocation: WitneyWorking Days: Mon-FriPay Rate: £30,000 Main Purpose of RoleThe primary objective of this role is to deliver high-quality and efficient data management support to Clinical Affairs, the Science Support Group, and other departments as needed.Main ResponsibilitiesPerform and oversee the upload and verification of data from multiple sources.Monitor the entry and migration of clinical data, collaborating with

Job Title: Medical Safety Analyst DevicesLocation: SittingbournePay Rate: £23-£30 per hourDuration: 12 MonthsResponsibilities:Process consumer complaints related to enteral feeding medical devices in accordance with applicable regulations.Collect, assess, and document medical device complaints and adverse events promptly and compliantly.Conduct follow-up calls with customers to gather additional details on adverse events and complaints.Code complaints usin

Are you an experienced sales professional looking to join a leading pharmaceutical company?  Do you have a successful track record in pharmaceutical sales and customer experience?If you're passionate about driving growth and advancing your career as a sales operations manager, we want to hear from you! Apply now!

Are you an experienced quality administrator or engineer? Do you have experience in managing multiple records from a document control and data entry point of view? We are recruiting for an Associate Quality Engineer to be accountable for supporting QA Engineers', Lead QA Engineers' and QA Managers' activities. This includes supporting the development and maintenance of their Quality System procedures for Design Control, Process Validation, Software Validat

Job Title: Product Support InvestigatorLocation: DundeePay rate: £12.83Work days: Mon-FriShift Pattern: 08:30 - 16:30 Main Purpose of Role:The Product Support Investigator is responsible for logging, assessing the reportability of end-user complaints, and conducting investigations in accordance with site procedures and regulations.Main Responsibilities:Log, acknowledge, and assess alleged product deficiencies from end users for adverse event reportability

Are you an experienced Quality Document Manager? Or, do you have a background in Medical Writing? If so, our Biotechnology client is looking for individuals just like you! The successful candidate will perform quality review to ensure documents authored by the Safety Surveillance and Aggregate Reports team or their vendors are of high quality and support process improvement. This is a contract position offered initially on a 12 month contract basis working

Are you an experienced sales professional looking to join a leading pharmaceutical company? Are you self-motivated and ready to take on responsibilities independently? Do you have a successful track record in pharmaceutical sales?If you're passionate about driving growth and advancing your career as a Business Development Area Manager, we want to hear from you! Apply now!

社名社名非公開職種生産企画、生産管理、工場長業務内容Head of PackagingMultinational pharmaceutical and biotechnology companyTasks:Lead team members and assure producing high quality products based on GMP and HSE requirements. To adopt the most effective process (mfg. method), acquiring the most reliable high technology and information, and implement validations for packaging process based on GMP. To assure the stable supply and product volume by controlling operation schedule and pe

社名社名非公開職種経営、事業部長、事業戦略企画業務内容Rare disease focused companyInnovationPatient Centricity求められる経験3+ years of work experience in the CRM field of a pharmaceutical companyPharmaceutical industry data knowledgeUnderstanding marketing and sales processes in pharmaceutical companiesQuantitative analysis skills and data driven thinkingBasic database skills SQL, Excel skillsExperience implementing BI tools (Business Object, MicroStrategy, Power BI, etc.)Data agency and

社名社名非公開職種薬事、メディカルライティング業務内容Key ResponsibilitiesPricing:As the Pricing lead for select inline brands and pipeline assets, work with internal partners and external stakeholders to establish and maintain optimal pricing and value of medicines.• Develop, lead and execute new drug price strategy as part of a broader Integrated Access Strategy including NHI drug price applications• In collaboration with Value, Access and Pricing (VAP) teams, co-develop and suppo

Do you acquire experience within the Regulatory Affairs sector? Is working in one of the most well established multinational companies a career goal for you? If the answer is yes, then look no further!We have the ideal job for you. Our client is looking for an experienced and skilled professional to join the Regulatory Affairs department as a Regulatory Affairs CW.

社名社名非公開職種営業(MR、MS、医療機器)、営業推進業務内容大手外資系製薬企業グローバルな環境求められる経験【経験・職務に必要な能力】University degree or aboveAt least 3 years of experience in Commercial CRM management in pharmaceutical industryDeep knowledge of CRM solutions (Veeva solution experience is preferred)Experience in BI development in pharmaceutical industry in preferredExperience in outsourcer or offshoring managementExperience in SFE (Sales Force Effectiveness) preferredExperience in Digital / Omnichannel

社名社名非公開職種業務内容One of the largest multinational pharmaceutical companies in the world is looking for an experienced legal counsel to join their team. Native-level Japanese and business level English are required for this role.求められる経験Over 6 years of legal experience, preferably some of it in the pharmaceutical industry.保険雇用保険休日休暇祝日給与年収1,000 ～ 1,500万円賞与discretionary

社名社名非公開職種プロジェクトマネージャー、ディレクター業務内容Project Management Specialist Product Supply at Global PharmaceuticalcompanyYOUR TASKS AND RESPONSIBILITIES:• Lead and support projects in the Product Supply department which are related to new launching products,manufacturing site transfer, inheritance products, divestment products, etc. in Pharmaceutical and ConsumerHealth business.• Coordinate and build consensus of project matters among stakeholders (e.g. Marketing, Regu

For our client, an internationally-active pharmaceutical company, specializing in niche areas such as hematology and oncology, we are looking for a:Senior Quality Assurance SpecialistLocation: Basel-CountryContract: permanentYour tasks:Your main responsibilities will include:Managing the Quality Management Manual documentation independentlyMonitoring and tracking complaints, deviations, and resulting measures (CAPA)Implementing changes (Change Control) wit