Supervisor QA Systems & Compliance
Lengnau
Key information
- Publication date:21 August 2025
- Workload:100%
- Place of work:Lengnau
Job summary
Join Thermo Fisher Scientific as a Supervisor QA Systems & Compliance. Be part of a company leading in science and innovation.
Tasks
- Oversee compliance activities at the Lengnau site for quality assurance.
- Make critical decisions impacting product compliance and quality.
- Lead QA activities including audits, metrics, and risk management.
Skills
- Master’s degree in life science or equivalent experience required.
- Over 10 years in the pharmaceutical industry with cGMP knowledge.
- Strong understanding of quality practices and health authority guidelines.
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Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office
Job Description
Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. And with over $1 billion invested annually in R&D, we empower our teams to put science into meaningful action and give our R&D colleagues the autonomy, resources and tools they need to take science a step beyond.
Position Purpose
This is a remarkable opportunity to join Thermo Fisher Scientific Inc. as a Supervisor QA Systems & Compliance. In this role, you will oversee and supervise compliance activities within our Lengnau site, ensuring our processes meet the highest standards of quality and reliability. You will interact with varying levels of staff within the organization, as well as customers and auditors, to strictly determine and successfully implement outstanding compliance processes.
Key Responsibilities
- Coordinate and supervise compliance activities within the Lengnau site.
- Make critical decisions regarding process compliance to impact product quality.
- Coordinate or lead QA activities including quality agreements, metrics, self-inspection, inspection readiness programs, supplier qualification, auditing, record review, final product functions, complaints, document management, risk management, and oversight of quality systems and investigations within QA.
- Manage the lifecycle of associated concepts/programs, policies, and procedures.
Education
- A Master's degree in a life science field is required. Equivalent work experience and knowledge can substitute.
Experience & Proficiencies
- More than 10 years of proven experience in the pharmaceutical industry.
- Excellent knowledge of Operations and Quality Assurance for biological pharmaceuticals (cGMP) with over 5 years of experience.
- In-depth knowledge of Quality practices, cGMP regulations, and international health authority guidelines (especially Swissmedic and US FDA).
Additional Requirements
- On-call services (picket light / 2nd level remote), based on department organization.
