Aktuelle Jobs im Zusammenhang mit MOS Compliance Expert - CorsiersurVevey - Randstad
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QA Qualification et Validation Expert
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Corsier-sur-Vevey, Schweiz Randstad - Medium prio VollzeitJobdescription An 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...
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Corsier-sur-Vevey, Schweiz Randstad VollzeitJobdescriptionAn exciting new opportunity has arisen to joinus as Quality Assurance Qualification & Validation Engineer forour Biotech drug substance plant in Corsier-sur-Vevey.As an integral member of the Quality Unit, you provide QAexpertise for Process Validation and AnalyticalValidation: Youelaborate the qualification/validation strategies, review...
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Quality Assurance Csv
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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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Quality Assurance Expert
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Quality Assurance Specialist
vor 3 Wochen
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Quality Assurance and Validation Specialist
vor 2 Wochen
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Swiss Tax Manager
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Swiss Tax Manager
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MOS Compliance Expert
vor 3 Monaten
As a MOS Compliance Expert at Merck, you will play apivotal role in the Production department, especially in theCompliance field, by conducting critical and transversal complexinvestigations, ensuring data integrity, leading Corrective andPreventive Actions (CAPA), maintaining compliance with GoodManufacturing Practices (GMP), and overseeing classifiedenvironment monitoring activities. Your responsibilities will alsoinclude overseeing project quality, managing Change ControlProcesses (CCP), and leveraging your proficiency in both French andEnglish.
KeyResponsibilities:
• Conduct Complex and Criticalcomprehensive investigations into quality and compliance incidents,identifying root causes and implementing effectivesolutions.
• Take charge of leading and managingCorrective and Preventive Actions (CAPA) to address quality andcompliance issues.
• Spearhead efforts to ensuredata integrity and compliance with regulatory standards in allaspects of operations.
• Maintain compliance withGood Manufacturing Practices (GMP) and other relevantregulations.
• Oversee project quality to ensurestrict adherence to quality standards and regulatoryrequirements.
• Manage Change Control Processes(CCP)
• Monitor classified environments to ensurecompliance with security and regulatorystandards.
• Utilize proficiency in both Frenchand English to effectively communicate and collaborate withstakeholders across different regions.
Functie-eisenQualifications:
- Bachelor'sdegree in a relevant field (e.g., pharmaceutical sciences,chemistry, biology, or related field).
- 4 to 5years of working experience in the pharmaceutical industry,demonstrating a strong background in compliance includinginvestigations processes, Stakeholder management, and regulatorystandards.
- In-depth knowledge of Investigationprocess, data integrity, CAPA, GMP andCCP.
- Proficiency in both French and English,with excellent written and verbal communicationskills.
- Strong analytical and problem-solvingabilities, with a keen attention todetail.
- Ability to thrive in a fast-paced,dynamic environment and collaborate effectively withcross-functional teams.