Aktuelle Jobs im Zusammenhang mit Regulatory Et Inspection Readiness Expert - CorsiersurVevey - Merck KGaA Darmstadt Germany
-
Regulatory Et Inspection Readiness Expert
vor 4 Monaten
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...
-
Regulatory Intelligence Expert
vor 2 Wochen
Villars-sur-Glâne, Freiburg, Schweiz Richemont VollzeitAbout the RoleWe are seeking a highly skilled Regulatory and Materials Expert to join our team at Richemont. As a key member of our GPTC Regulatory Team, you will play a crucial role in ensuring the reliability of information in our Group Materials' Data Base.Key ResponsibilitiesCollaborate with the GPTC Regulatory Team Experts to establish and maintain...
-
MOS Compliance Expert
vor 1 Monat
Corsier Sur Vevey, Schweiz Randstad VollzeitAs a MOS Compliance Expert at Merck, you will play a pivotal role in the Production department, especially in the Compliance field, by conducting critical and transversal complex investigations, ensuring data integrity, leading Corrective and Preventive Actions (CAPA), maintaining compliance with Good Manufacturing Practices (GMP), and overseeing classified...
-
MOS Compliance Expert
vor 4 Wochen
Corsier Sur Vevey, Schweiz Randstad VollzeitAs a MOS Compliance Expert at Merck, you will play a pivotal role in the Production department, especially in the Compliance field, by conducting critical and transversal complex investigations, ensuring data integrity, leading Corrective and Preventive Actions (CAPA), maintaining compliance with Good Manufacturing Practices (GMP), and overseeing classified...
-
Regulatory and Materials Expert
vor 1 Monat
Villars-sur-Glâne, Schweiz Richemont VollzeitHow will you make an impact? HOW WILL YOU MAKE AN IMPACT? As a “Regulatory & Materials’ Expert” within the GPTC Regulatory Team, you will participate to ensure the reliability of the information set in the Group Materials’ Data Base from both a Product & Trade Compliance and Nomenclature perspectives. The first refers to the identification and...
-
Regulatory and Materials Expert
vor 2 Wochen
Villars-sur-Glâne, Freiburg, Schweiz Richemont VollzeitAbout the RoleWe are seeking a highly skilled Regulatory and Materials Expert to join our team at Richemont. As a key member of our GPTC Regulatory Team, you will play a crucial role in ensuring the reliability of information in our Group Materials' Data Base.Key ResponsibilitiesCollaborate with the GPTC Regulatory Team Experts to establish and maintain...
-
Analytical Op&qc Raw Material Expert
vor 3 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...
-
Regulatory and Materials Expert
vor 2 Monaten
Villars-sur-Glâne, Schweiz Richemont VollzeitThe Regulatory Team (RT) of the Group Product & Trade Compliance department (GPTC) provides regulations’ monitoring, regulatory expertise & compliance solutions to the Richemont Group’s internal stakeholders (Maisons, Regions and other Group functions) on multiple regulatory fields, incl. Product Safety (e.g. CE, UKCA, ROHS, REACH, TSCA, SABER, TAREKS) &...
-
Quality Operation Associate Manager
vor 4 Monaten
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...
-
Internship Lab Equipment Expert
vor 4 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...
-
MOS Compliance Expert
vor 1 Monat
Corsier-sur-Vevey, Schweiz Randstad VollzeitJobdescriptionAs 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...
-
Quality Assurance Csv
vor 4 Monaten
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...
-
Qc Biochemistry Expert
vor 4 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...
-
Quality Assurance Csv
vor 4 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...
-
QA Qualification et Validation Expert
vor 4 Wochen
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...
-
QA Qualification et Validation Expert
vor 1 Monat
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...
-
QA Qualification et Validation Expert
vor 3 Wochen
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...
-
QC Support Compliance Investigation Engineer
vor 1 Monat
Corsier-sur-vevey, Schweiz Randstad VollzeitWe are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related...
-
QC Support Compliance Investigation Engineer
vor 1 Monat
Corsier-sur-vevey, Schweiz Randstad VollzeitWe are seeking a highly skilled and experienced QC Support Investigation Expert to join our Quality Control team. The ideal candidate will have a strong engineering background and extensive experience in the pharmaceutical or biotech industry. The primary responsibility of the QC Support Investigation Expert will be to lead and support investigations related...
-
QA Operation Specialist
vor 3 Wochen
Corsier-sur-Vevey, Schweiz Randstad VollzeitDescription du postePour notre client basé à Corsier-sur-Vevey, au seinde l'équipe QA Operations, nous sommes à la recherche de plusieursQA Operations Specialist pour une durée de 12 à jusqu'à 24 mois.En tant que membre de l'équipe, vous assurez laconformité et la documentation des activités de lié à lafabrication sur le site. Vous travaillerez...
Regulatory Et Inspection Readiness Expert
vor 3 Monaten
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.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility.
Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life.
Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Your role:
Site Regulatory compliance activities:
- Ensure Quality/CMC consistency and compliance by liaising with the Global Regulatory Affairs department. You will support the establishment of Regulatory reporting (e.g. Annual Reports) and Regulatory Affairs requests (e.g. renewals process, statements, GMP certificates).
- Provide the regulatory status overview for products portfolio to the Qualified Person of the site in the frame of product disposition process.
Inspection Readiness activities:
- Lead the site Quality inspections readiness program, from notification by the inspection body until approval of the CAPA plan
- Central member of the audit/inspection hosting team
- Coordinate and followup the definition and execution of CAPA plans
Who you are:
- Degree in a Life Science or related discipline (minimum MSc or equivalent degree), higher degree preferable (e.g. PhD in a scientific discipline)
- You have at least 57 years of experience in the pharmaceutical industry
- You have at least 5 years of experience in global CMC regulatory affairs, and quality assurance / compliance, inclunding experience in inspection readiness.
- Experience with lifecycle management activities in at least two regions (e.g. Europe, USA, or International)
- Good knowledge in biotechnological sciences, manufacturing of biologics and related regulatory guidelines (cGMPs, 21 CFR, etc.)
- Excellent written and spoken communication skills in English
What we offer:
We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences.
We celebrate all dimensions of diversity and believe that it drives excellence and innovation, strengthening our ability to lead in science and technology.
We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress