Aktuelle Jobs im Zusammenhang mit Regulatory Compliance Specialist - Neuenburg, Neuenburg - RM Group (Switzerland)
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Regulatory Compliance Manager
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Senior Manager QA/RA Projects
vor 4 Wochen
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Senior Manager QA/RA Projects
vor 4 Wochen
Neuenburg, Neuenburg, Schweiz Gi Group SA VollzeitFor our partner in pharmaceutical industry, Gi Life Science is looking for a:Senior Manager QA/RA Projects(Permanent position)Your mission:· Ensure that each product is continuously manufactured, packaged, and tested in compliance with the Marketing Authorisation Dossier managed by the Customer/Product Owner and also to support the site in...
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Senior Manager QA/RA Projects
vor 2 Stunden
Neuenburg, Neuenburg, Schweiz Gi Group SA VollzeitFor our partner in pharmaceutical industry, Gi Life Science is looking for a:Senior Manager QA/RA Projects(Permanent position)Your mission:· Ensure that each product is continuously manufactured, packaged, and tested in compliance with the Marketing Authorisation Dossier managed by the Customer/Product Owner and also to support the site in...
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Senior Compliance Engineer
vor 6 Stunden
Neuenburg, Neuenburg, Schweiz Michael Page VollzeitAbout Gi Life SciencesGi Life Sciences is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world.Job DescriptionThe Senior Engineer will be responsible for authoring, owning and leading updates of GMP documents related to...
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Compliance and Governance Specialist
Vor 3 Tagen
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Project Lead for Neuchatel Plant Extension
Vor 3 Tagen
Neuenburg, Neuenburg, Schweiz Randstad VollzeitAbout the RoleWe are looking for a seasoned Project Lead for Neuchatel Plant Extension to lead the technical aspects of our new plant extension project at the Neuchatel site.The successful candidate will have a strong background in project management and experience working on complex projects in the pharmaceutical industry.You will be responsible for leading...
Regulatory Compliance Specialist
vor 1 Woche
About Our Company
R M Group is a leading company in the pharmaceutical sector based in Neuchâtel, Switzerland. We offer a range of opportunities for talented professionals who share our commitment to quality and excellence.
Job Summary
We are seeking a skilled QC Associate Scientist to join our team. The successful candidate will be responsible for laboratory investigations, critical material qualification, and laboratory method transfers.
Your Key Responsibilities
- Laboratory Investigations: Conduct experiments, analyze data, and document results.
- Critical Material Qualification: Author qualification plans and reports for critical reagents, oversee validation and qualification activities executed by analysts, and provide training and support.
- Laboratory Method Transfers: Supports daily QC activities following cGMP, policies, and EHS requirements.
- Documentation: Author transfer protocols and reports for assays, execute and document experiments, and investigate and troubleshoot problems which occur to determine solutions or recommendations for improvements or change.
Your Requirements
- University or engineering degree in analytical chemistry, biotechnology, biochemistry, or microbiology.
- 1-2 years of experience in GMP pharma business activities, preferably in the scope of recombinant therapeutic product in pharmaceutical environment.
- Experience in GMP Laboratory activities, good knowledge of method transfer, and critical reagent qualification.
- Excellent problem-solving skills, experience in problem solving and deviation management, and good knowledge of statistical tools.
Benefits
- A competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and collaborative work environment.