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16228en
- Contract
- German
- Associate
- Research & Development
- Switzerland
- Healthcare & Life Sciences
Skills
QA, Batch Record Management, Pharma, Biotech, GMP
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Join a Leading Biopharma Company as a QA Specialist / Batch Record Reviewer!
Contract Type: Contract
Start Date: ASAP
Location: Visp
Workload: 100%
Duration: Until 31/03/2025
Your Mission:
• Review executed electronic and/or manufacturing protocol for compliance to GMP.
• Support implementation/revision of manufacturing protocols for GMP manufacturing.
• Ensure that internal/external GMP standards and regulatory requirements are adhered to in projects.
• Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures.
• Represent the Quality Unit in cross-functional teams.
• Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams.
• Review and approve validation documents.
Your background:
• Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry.
• Previous experience in GMP regulated pharmaceutical industry is an advantage.
• English fluency and German good command are an advantage.
• Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
• Excellent verbal, written and interpersonal communications skills.
If this sounds like you, don’t hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
Contract Type: Contract
Start Date: ASAP
Location: Visp
Workload: 100%
Duration: Until 31/03/2025
Your Mission:
• Review executed electronic and/or manufacturing protocol for compliance to GMP.
• Support implementation/revision of manufacturing protocols for GMP manufacturing.
• Ensure that internal/external GMP standards and regulatory requirements are adhered to in projects.
• Participate in cross-functional investigations to determine impact to product quality and the definition of associated corrective measures.
• Represent the Quality Unit in cross-functional teams.
• Make independent quality-related decisions based on regulatory and compliance knowledge and provide independent quality support to project teams.
• Review and approve validation documents.
Your background:
• Degree in Biology, Chemistry, Biotechnology, Life Science or other related field or experience in the field of pharmaceutical industry.
• Previous experience in GMP regulated pharmaceutical industry is an advantage.
• English fluency and German good command are an advantage.
• Ability to prioritize and manage work to critical project timelines in a fast-paced environment.
• Excellent verbal, written and interpersonal communications skills.
If this sounds like you, don’t hesitate to apply here or reach out directly to Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com.
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