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vor 4 Wochen
Corsier-sur-Vevey, Schweiz Randstad (Schweiz) AG VollzeitDescription du postePour le département Data & Digital , nous recherchons un " Compliance Engineer " sur le site Merck à Corsier sur Vevey :Mission :Participation au suivi des items Qualité de l'équipe Data & Digital tel que la rédaction des investigations de déviations, des actions correctives et préventives (CAPA), ainsi que les actions de CCP liés...
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Vor 6 Tagen
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Compliance Engineer
vor 1 Monat
Vevey, Schweiz Randstad VollzeitDescription du postePour le département Data & Digital , nousrecherchons un " Compliance Engineer " sur le site Merck à Corsiersur Vevey :Mission:Participation au suivi des itemsQualité de l’équipe Data & Digital tel que la rédaction desinvestigations de déviations, des actions correctives etpréventives (CAPA), ainsi que les actions de CCP liés aux...
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Quality Assurance Csv
vor 5 Monaten
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Quality Assurance Csv
vor 5 Monaten
Corsier-sur-Vevey, Schweiz Merck KGaA VollzeitWork Your Magic with us! Ready to explore, break barriers, and discover more? We know you've got big plans '“ so do we! Our colleagues across the globe love innovating with science and technology to enrich people's lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix...
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QA Qualification et Validation Expert
vor 2 Monaten
Corsier-sur-vevey, Schweiz Randstad VollzeitAn exciting new opportunity has arisen to join us as Quality Assurance Qualification & Validation Engineer for our Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QA expertise for Process Validation and Analytical Validation: You elaborate the qualification/validation strategies, review and approval...
QC Support Compliance Engineer
vor 3 Monaten
As a key member of the organization, you'll be part of a diverse team in a dynamic, global environment. Your role involves:
Serving as a compliance representative for the quality control department and QC Support TeamLeading deviations, CAPA, and periodic reviews related to our activitiesProviding training in CCP, CAPA, and investigationsEnsuring compliance for the QC support Group and the Quality Control DepartmentContributing to the continuous improvement of quality control support processes and proceduresReviewing and approving internal documents and agreements
Participating in equipment and material qualification
Acting as a quality project manager to proactively identify and resolve problems
Collaborating with various functions and stakeholders
Serving as an expert for deviation, change control, and CAPA topics during health authority inspectionsBackup for other QC support compliance, autonomously resolve compliance issues promptly, contribute to continuous improvement using a lean process mindset, and actively participate in performance management meetings to drive improvement.
Qualifikationen Eng. in sciences (chemistry, biology) or 3+ years of experience in a GMP environmentMinimum 1 year expertise in the biotech industry
Precise, rigorous, and detail-oriented
Team player with the ability to collaborate across departments
Experience in quality control and quality systems
Experience in planning tools is a plus
Good knowledge of visual management
Familiar with applicable cGMPs
Fluent in French and English
Process-oriented with a strong customer service focus
Proficient in problem-solving tools and ensuring their use in the group
Result-driven with a "can do" attitude
Autonomous, reliable, and highly motivated
Positive and collaborative communication within the team and with partners/customers