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16400en
- Contract
- English
- Mid-Senior level
- Research & Development
- Zurich
- Healthcare & Life Sciences
Skills
QA, QualityGMP, Pharma, Biotech, Regulatory Compliance
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On behalf of our client, a global leader in the pharmaceutical industry, Swisslinx is seeking a QA Manager to join their dynamic team. In this role, you will take a central position in managing quality oversight of external partners and driving continuous improvement.
Contract type: Contract
Start Date: ASAP
Locations: Zürich, Switzerland / twice per month: Singen, Germany
Workload: 100%
Duration: 1.5 years
Your mission:
• Perform GMP-compliant batch record review and approval for externally manufactured products within Vaccine External Supplier Quality (ESQA).
• Ensure timely batch evaluation and preparation of documents for batch release by regulatory authorities.
• Manage deviations, changes, CAPAs, and other QMS documents for external products.
• Maintain daily collaboration and communication with external partners, representing the company professionally.
• Coordinate complaint handling with external partners and global/local functions.
• Support regulatory inspections, internal inspections, and global audits at external partners.
• Facilitate documentation required by the regulatory department for registration purposes.
• Oversee and coordinate Quality Agreements (QAGs).
• Contribute to the development of global quality metrics/KPIs for external partners.
Your background:
• Degree in Pharmacy, Microbiology, Life Sciences, or a related scientific discipline.
• Several years of professional experience in Quality Assurance, Quality Oversight, or Regulatory Compliance, ideally in the pharmaceutical/biotech industry.
• Solid knowledge of GMP regulations.
• Demonstrated written and oral communication skills and ability to work in a cross-functional team environment.
• Strong interest and commitment to digital transformation and continuous improvement through data analytics and automation is a plus.
• Capable of thriving in a fast-paced environment with minimal supervision.
• Precise, reliable working style and a team-oriented mindset.
• Fluent English is required; additional languages are an advantage.
What’s on offer:
• 1.5-year fixed-term contract with a leading global pharmaceutical company.
• Opportunity to grow and develop your career in a dynamic and international environment.
• Work across Zürich or Singen, collaborating with an expert team on impactful projects.
If this sounds like you, don’t hesitate to apply here or contact Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com
Contract type: Contract
Start Date: ASAP
Locations: Zürich, Switzerland / twice per month: Singen, Germany
Workload: 100%
Duration: 1.5 years
Your mission:
• Perform GMP-compliant batch record review and approval for externally manufactured products within Vaccine External Supplier Quality (ESQA).
• Ensure timely batch evaluation and preparation of documents for batch release by regulatory authorities.
• Manage deviations, changes, CAPAs, and other QMS documents for external products.
• Maintain daily collaboration and communication with external partners, representing the company professionally.
• Coordinate complaint handling with external partners and global/local functions.
• Support regulatory inspections, internal inspections, and global audits at external partners.
• Facilitate documentation required by the regulatory department for registration purposes.
• Oversee and coordinate Quality Agreements (QAGs).
• Contribute to the development of global quality metrics/KPIs for external partners.
Your background:
• Degree in Pharmacy, Microbiology, Life Sciences, or a related scientific discipline.
• Several years of professional experience in Quality Assurance, Quality Oversight, or Regulatory Compliance, ideally in the pharmaceutical/biotech industry.
• Solid knowledge of GMP regulations.
• Demonstrated written and oral communication skills and ability to work in a cross-functional team environment.
• Strong interest and commitment to digital transformation and continuous improvement through data analytics and automation is a plus.
• Capable of thriving in a fast-paced environment with minimal supervision.
• Precise, reliable working style and a team-oriented mindset.
• Fluent English is required; additional languages are an advantage.
What’s on offer:
• 1.5-year fixed-term contract with a leading global pharmaceutical company.
• Opportunity to grow and develop your career in a dynamic and international environment.
• Work across Zürich or Singen, collaborating with an expert team on impactful projects.
If this sounds like you, don’t hesitate to apply here or contact Veronika von Mentzer, Recruiter: veronika.nakev@swisslinx.com
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