Quality Assurance Manager (m/d/f) 80%
Publication date:
22 April 2025Workload:
80%Contract type:
Unlimited employment- Place of work:Kaiseraugst
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Job summary
Join Solvias, a leader in contract research for analytical services. Enjoy a dynamic work environment with flexible hours and growth opportunities.
Tasks
- Review and approve quality documents like SOPs and reports.
- Support quality investigations of deviations and OOS issues.
- Manage customer audits and interpret compliance requirements.
Skills
- Master's degree in analytical chemistry or life sciences required.
- Strong problem-solving and interpersonal skills essential.
- Experience with GMP regulations and quality systems needed.
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Solvias is a world leader in contract research for analytical services. The industries we serve include pharmaceuticals, biotech, medical devices, cosmetics, chemical, electronic materials, life sciences and oil. With a well-established scientific experience and proven track record, we provide integrated services, products and technologies to enhance the value chain for customers worldwide.
Our Quality Assurance department is looking for a dynamic professional personality as Quality Assurance Manager.
Quality Assurance Manager (m/d/f) 80%
- Review and approval of SOPs, protocols, reports, Certificate of Analysis and other quality documents
- Support quality investigation of deviations and Out of Specification (OOS)
- Maintenance, recording and processing of corrective and preventive measures (CAPA)
- Organization and management of customer audits, and inspections
- Apply and interpret audit and compliance requirements
- Act as QA point of contact for customers
- Support for GMP training
- System Administration of Quality Management Software
- Scientific education (Master degree) in analytical chemistry / biochemistry / life science
- Multi-year, industrial work experience of 7 years minimum in the analytical-pharmaceutical environment preferably experience in QA
- Strong problem-solving skills to meet business objectives
- Excellent interpersonal skills and teamwork spirit
- Ability to collaborate in a dynamic, cross-functional matrix environment
- Broad knowledge and proven experience of the regulatory framework in the GMP environment (ICH, FDA, USP, Ph. Eur.)
- Solid background in data integrity and computerized systems risk assessment and project support
- Experience as system administrator or deeper IT knowledge is an asset
- Fluency in English and wiliness to learn German is required
- a well-structured onboarding program
- intensive training in the beginning
- the possibility for further development
- flexible working time models
- 40 hours week
- at least 28.5 vacation days per year (depending on your age)
- commuter contribution for using public transport
- staff restaurant
We offer attractive working conditions and flexible working hours and believe that our employees make the difference. Everyone can contribute, influence and grow both professionally and personally. Do you feel addressed? Then we look forward to your complete online application documents.