QA qualification and validation expert
Vor 3 Tagen
JobdescriptionAn exciting opportunity has arisen to join us as Quality Assurance Qualification Expert for our Biotech drug substance plant in Corsier-sur-Vevey.Your role:As an integral member of the Quality Unit, you provide QA expertise for Equipment Qualification/Requalification, Sterilization qualification, Cleaning Validation, Raw Material Qualification, Process & Analytical Validation, and Computerized System Validation.The role consists to elaborate the qualification/validation strategies, review and approval of protocols and reports, participates to risk analysis, identifies gap and purposes remediation plan. You act as Quality Subject Matter Expert on specific topics and participate in risk assessments and handle deviations on these topics. You review and/or approve qualification/validation documents, risk assessment, SOPs and take quality decisions according to company standards.The activities of the QA Expert cover all qualification/validation phases from Basic Design until 1st use of equipment/raw material.10. You ensure GMP compliance during all phases of qualification/validation. QualifikationenWho you are: University or relevant engineering degree Hands on experience of equipment Qualification/Validation in the pharmaceutical industryAt least 2 years' experience in a quality environment in pharmaceutical industry or equivalent, ideally in biotechnologyKnowledge in cGMP and health authority expectations,Knowledge in Data Integrity will be a plusExperience in Equipment (Utilities/E&M/Production/Lab equipment)Good interpersonal skills, with a positive attitude and the ability to support his colleagues in a context of growth and changesGood writing skills.French written & spoken, English good written skills.
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QA qualification and validation expert
Vor 2 Tagen
Corsier-sur-Vevey, Schweiz Randstad VollzeitJobdescription An exciting opportunity has arisen to join us as Quality Assurance Qualification Expert for our Biotech drug substance plant in Corsier-sur-Vevey. Your role: As an integral member of the Quality Unit, you provide QA expertise for Equipment Qualification/Requalification, Sterilization qualification, Cleaning Validation, Raw Material...
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Qa qualification and validation expert
vor 8 Stunden
Corsier-sur-vevey, Schweiz Randstad VollzeitJobdescription An exciting opportunity has arisen to join us as Quality Assurance Qualification Expert for our Biotech drug substance plant in Corsier-sur-Vevey. Your role: As an integral member of the Quality Unit, you provide QA expertise for Equipment Qualification/Requalification, Sterilization qualification, Cleaning Validation, Raw Material...
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QA qualification and validation expert
Vor 3 Tagen
Corsier-sur-Vevey, Schweiz InGoedeBanen.nl VollzeitJobdescriptionAn exciting opportunity has arisen to join us asQuality Assurance Qualification Expert for our Biotech drugsubstance plant in Corsier-sur-Vevey.Yourrole:As an integral memberof the Quality Unit, you provide QA expertise for EquipmentQualification/Requalification, Sterilization qualification,Cleaning Validation, Raw Material Qualification,...
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Qa qualification and validation expert
vor 8 Stunden
Corsier-sur-vevey, Schweiz Randstad VollzeitJobdescription An exciting opportunity has arisen to join us as Quality Assurance Qualification Expert for our Biotech drug substance plant in Corsier-sur-Vevey. Your role: As an integral member of the Quality Unit, you provide QA expertise for Equipment Qualification/Requalification, Sterilization qualification, Cleaning Validation, Raw Material...
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Quality Assurance Csv
Vor 2 Tagen
Corsier-sur-Vevey, Schweiz Merck KGaA Darmstadt Germany 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 of...
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Quality Assurance Csv
Vor 2 Tagen
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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Validation Engineer
Vor 3 Tagen
Vevey, Waadt, Schweiz Panda International VollzeitValidation Engineer (Lab Equipment) | Leading Global Biotech ManufacturerAbout the RoleA leading global biotech manufacturer in Switzerland is seeking aLab Equipment Specialistto support engineering, maintenance, and laboratory qualification activities within a GMP-regulated environment.This junior-level position focuses onCQV activities, equipment...
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Analytical Op&qc Digital Expert
vor 2 Wochen
Corsier-sur-Vevey, Schweiz Merck Group VollzeitExpress your talent with us! Do you want to explore, overcome obstacles, and make discoveries? We know that your projects are ambitious. Ours are too! Around the world, our colleagues share a passion for scientific and technological innovation that enriches human lives through our solutions in Healthcare, Life Science, and Electronics. Together, we think big...
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Qc Physico-chemistry Expert
vor 20 Stunden
Corsier-sur-Vevey, Schweiz Merck Group 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...
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QA Operations Lead – GMP Compliance
vor 2 Wochen
Corsier-sur-Vevey, Schweiz Merck Gruppe VollzeitA leading healthcare firm in Switzerland seeks a Quality Assurance professional to ensure compliance with GMP standards at its Vevey site. This role includes managing QA operations, leading deviation management processes, and participating in audits. Ideal candidates will have an advanced technical degree, significant QA experience in a GMP environment, and...