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16446en
- Contract
- English
- Associate
- Research & Development
- Switzerland
- Healthcare & Life Sciences
Skills
QA, Quality Assurance, GMP, Batch Record Review, CAPAs
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On behalf of our client, we are seeking a skilled and motivated QA Specialist to join their team in Visp. This is an exciting opportunity to work in a dynamic environment with a global leader in healthcare and life sciences. The successful candidate will play a key role in ensuring the highest quality standards are met across various operations in a GMP-regulated setting.
Location: Visp, Switzerland
Contract Type: Contract
Start Date: ASAP
Workload: 100%
Your Responsibilities:
• Support quality assurance activities across manufacturing and operational processes to ensure compliance with GMP and regulatory requirements.
• Review and approve batch records, deviations, CAPAs, and change controls.
• Conduct quality oversight and risk assessments to ensure consistent adherence to quality standards.
• Collaborate with cross-functional teams to resolve quality-related issues and implement improvements.
• Participate in internal and external audits, providing expertise and documentation as needed.
• Ensure accurate and compliant documentation within the quality management system.
Your Background:
• Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, or Engineering).
• 2–5 years of experience in quality assurance within a GMP-regulated environment, preferably in the pharmaceutical or biotech industry.
• Strong knowledge of GMP standards and regulatory guidelines.
• Detail-oriented with excellent problem-solving and organizational skills.
• Fluent in English; knowledge of German is a strong advantage.
What’s on Offer:
• An opportunity to contribute to cutting-edge healthcare solutions with a leading global company.
• A supportive and innovative work environment.
• Opportunities for personal and professional growth.
If you are ready to advance your career in quality assurance and want to make an impact, we look forward to receiving your application.
For more information, please contact Veronika von Mentzer, Recruiter, at veronika.nakev@swisslinx.com.
Location: Visp, Switzerland
Contract Type: Contract
Start Date: ASAP
Workload: 100%
Your Responsibilities:
• Support quality assurance activities across manufacturing and operational processes to ensure compliance with GMP and regulatory requirements.
• Review and approve batch records, deviations, CAPAs, and change controls.
• Conduct quality oversight and risk assessments to ensure consistent adherence to quality standards.
• Collaborate with cross-functional teams to resolve quality-related issues and implement improvements.
• Participate in internal and external audits, providing expertise and documentation as needed.
• Ensure accurate and compliant documentation within the quality management system.
Your Background:
• Bachelor’s degree in a relevant field (e.g., Life Sciences, Pharmacy, or Engineering).
• 2–5 years of experience in quality assurance within a GMP-regulated environment, preferably in the pharmaceutical or biotech industry.
• Strong knowledge of GMP standards and regulatory guidelines.
• Detail-oriented with excellent problem-solving and organizational skills.
• Fluent in English; knowledge of German is a strong advantage.
What’s on Offer:
• An opportunity to contribute to cutting-edge healthcare solutions with a leading global company.
• A supportive and innovative work environment.
• Opportunities for personal and professional growth.
If you are ready to advance your career in quality assurance and want to make an impact, we look forward to receiving your application.
For more information, please contact Veronika von Mentzer, Recruiter, at veronika.nakev@swisslinx.com.
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