Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
At Thermo Fisher Scientific team, you'll discover impactful work, innovative thinking and a culture dedicated to working the right way, for the right reasons - with the customer always top of mind. The work we do matters, like helping customers find cures for cancer, protecting the environment, making sure our food is safe. As the world leader in serving science, with the largest investment in R&D in the industry, our colleagues are empowered to realize their full potential as part of a fast-growing, global organization that values passion and unique contributions. Our commitment to our colleagues across the globe is to provide the resources and opportunities they need to make a difference in our world while building a fulfilling career with us.
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Summary:
The role involves being responsible for client-facing activities within the Quality Assurance department, including participation in client audits. The position holder is also actively engaged in a range of compliance-related tasks within Fisher Clinical Services.
Location/Division : Allschwil, Switzerland, CTD
QA Audit Specialist
- Hosting client audits and ensuring a smooth audit process.
- Coordinating Corrective and Preventive Actions (CAPAs) in response to client audit findings.
- Conducting follow-up on CAPAs to ensure timely resolution and closure.
- Reviewing and approving investigation reports.
- Participating in projects, such as Process Performance Improvement (PPI) initiatives.
- Participating to internal audits as an Auditor/Support Team member, supporting the organization in audit execution, report writing, and the management of audit records in TrackWise.
Experience
- Proficiency in both written and spoken German and English.
- Minimum educational background in a scientific field with advanced qualifications.
- Strong analytical abilities to effectively assess challenges and propose solutions.
- Ability to thrive under pressure while providing support to team members.
- Excellent presentation, verbal and written communication skills
- Strong problem-solving skills and the ability to find effective solutions.
Education
- Bachelor of Science (B.Sc.) is preferred, or validated experience in GMP, GDP compliance and regulatory within the pharmaceutical industry.