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2 jobs found in Zug

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    • zug, zug
    • contract
    Are you a motivated Quality Control Specialist Manager and you are looking for your next career step in the Medical Device business?Are looking for a company where you have the opportunity to pursue your interests across functions and geographies? Then you should read on!Tasks & ResponsibilitiesAnalysis, documentation and review of sensor QC resultsMonitoring, analysis and handling of issues occurring during the release testsPreparation and execution of deviation notifications, variances, changes, out of specifications and CAPAsDrive and lead QC related topics and initiativesOrganizer, co-lead or representative of the QC department in several coordination meetingsWriting of SOPs and general documents, improvement of the QC processes and toolsCommunication and coordination with internal and external partners (e.g. production, quality assurance, engineering support and development)Must Haves:University degree in engineering, sciences or related fieldStrong affinity to work accurately, high quality awarenessExperience with GxP (especially good documentation practice)Team player with strong communication skills also across teams and departments Fluent in German and English oral and written Nice to Haves:Database handling and experience with software projectsExperience with statistical analysisCoordinative or lead experience in project or production environment Knowledge of lean methods Experience in quality control and/ or medical diagnostic applicationsHave we sparked your interest? We are looking forward to receving you application!
    Are you a motivated Quality Control Specialist Manager and you are looking for your next career step in the Medical Device business?Are looking for a company where you have the opportunity to pursue your interests across functions and geographies? Then you should read on!Tasks & ResponsibilitiesAnalysis, documentation and review of sensor QC resultsMonitoring, analysis and handling of issues occurring during the release testsPreparation and execution of deviation notifications, variances, changes, out of specifications and CAPAsDrive and lead QC related topics and initiativesOrganizer, co-lead or representative of the QC department in several coordination meetingsWriting of SOPs and general documents, improvement of the QC processes and toolsCommunication and coordination with internal and external partners (e.g. production, quality assurance, engineering support and development)Must Haves:University degree in engineering, sciences or related fieldStrong affinity to work accurately, high quality awarenessExperience with GxP (especially good documentation practice)Team player with strong communication skills also across teams and departments Fluent in German and English oral and written Nice to Haves:Database handling and experience with software projectsExperience with statistical analysisCoordinative or lead experience in project or production environment Knowledge of lean methods Experience in quality control and/ or medical diagnostic applicationsHave we sparked your interest? We are looking forward to receving you application!
    • rotkreuz, zug
    • contract
    Do you want to work in a big pharmaceutical company? Do you have experience in Quality Assurance? You should then read the following lines! Our client, based in Rotkreuz, is looking for a part-time QA manager for a 9 months contract.  The QA Release Manager prevents quality or regulatory non-compliance issues which could lead to product stock-out / withdrawal or product approval delays. He/she takes ownership of processes connected to marketed products, e.g. batch release, complaints handling, deviation management, escalation management and health authority notifications, as delegated by the Responsible Person (FvP). By building a strong network with internal and external stakeholders efficient business partnering is ensured and clear communication is provided. As project lead he/she drives compliance, cross-divisional standardization, innovation and operational excellence.  Your Tasks: Acts as Subject Matter Expert (SME) in his/her own area of responsibility.Responsible for the adequate handling and investigation of deviations including their CAPAs.Is responsible for maintaining and updating the quality management system within his/her area of responsibility.Ensures readiness for all GxP regulatory inspections & audits and performs self- inspections according to plan.Foster and champion a quality culture and a quality mindset.Batch Release: Responsible for the release and non-release of product batches of marketed goods as delegated by the Responsible Person (FvP).Returns: Responsible for the release and non-release of returned product, as delegated by the Responsible Person (FvP).Escalations: Is responsible for escalation and management of quality incidents. Represents the country in escalation calls, as delegated by the Responsible Person (FvP). This includes the follow-up on required activities for investigation and CAPAs as well as timely communication to local Health Authorities.Communication to Health Authorities: Is responsible for the timely communication with Health Authorities, as delegated by the Responsible Person (FvP).Interaction with stakeholders: Is responsible for the interaction and communication with internal (e.g. Customer Service / Regulatory Affairs / Supply Chain Management) and external (e.g. warehouse) stakeholders within own area of responsibility.Change Control (product / QA Release related): Is responsible to perform QA activities for product / QA Release related change requests.Launches: In case of more complex launches or quality issues: Represents local QA organization in the launch team, ensures QA activities for successful product launches.   Your Profile: • Master degree in pharmacy or comparable education/scientific background with experience in GxP area• Fluency in German and English (oral and written), French as advantage• Several (5) years professional experience in pharmaceutical industry, analytics, quality assurance, production, distribution or pharmacy.• Strong interpersonal, communication, negotiation and problem solving skills.• Strong project management skills, including simplification mindset, strategic thinking and ability to lead changes. 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 Quality Assurance? You should then read the following lines! Our client, based in Rotkreuz, is looking for a part-time QA manager for a 9 months contract.  The QA Release Manager prevents quality or regulatory non-compliance issues which could lead to product stock-out / withdrawal or product approval delays. He/she takes ownership of processes connected to marketed products, e.g. batch release, complaints handling, deviation management, escalation management and health authority notifications, as delegated by the Responsible Person (FvP). By building a strong network with internal and external stakeholders efficient business partnering is ensured and clear communication is provided. As project lead he/she drives compliance, cross-divisional standardization, innovation and operational excellence.  Your Tasks: Acts as Subject Matter Expert (SME) in his/her own area of responsibility.Responsible for the adequate handling and investigation of deviations including their CAPAs.Is responsible for maintaining and updating the quality management system within his/her area of responsibility.Ensures readiness for all GxP regulatory inspections & audits and performs self- inspections according to plan.Foster and champion a quality culture and a quality mindset.Batch Release: Responsible for the release and non-release of product batches of marketed goods as delegated by the Responsible Person (FvP).Returns: Responsible for the release and non-release of returned product, as delegated by the Responsible Person (FvP).Escalations: Is responsible for escalation and management of quality incidents. Represents the country in escalation calls, as delegated by the Responsible Person (FvP). This includes the follow-up on required activities for investigation and CAPAs as well as timely communication to local Health Authorities.Communication to Health Authorities: Is responsible for the timely communication with Health Authorities, as delegated by the Responsible Person (FvP).Interaction with stakeholders: Is responsible for the interaction and communication with internal (e.g. Customer Service / Regulatory Affairs / Supply Chain Management) and external (e.g. warehouse) stakeholders within own area of responsibility.Change Control (product / QA Release related): Is responsible to perform QA activities for product / QA Release related change requests.Launches: In case of more complex launches or quality issues: Represents local QA organization in the launch team, ensures QA activities for successful product launches.   Your Profile: • Master degree in pharmacy or comparable education/scientific background with experience in GxP area• Fluency in German and English (oral and written), French as advantage• Several (5) years professional experience in pharmaceutical industry, analytics, quality assurance, production, distribution or pharmacy.• Strong interpersonal, communication, negotiation and problem solving skills.• Strong project management skills, including simplification mindset, strategic thinking and ability to lead changes. 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.

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