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QA Specialist – GLP Bioanalysis
Job in
Germany, Pike County, Ohio, USA
Listed on 2026-01-02
Listing for:
Kymos Group
Full Time
position Listed on 2026-01-02
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst -
Healthcare
Data Scientist
Job Description & How to Apply Below
Location: Germany
Prolytic GmbH | Part of the Kymos Group
Prolytic GmbH is a specialized GLP-certified bioanalytical laboratory and has been part of the Kymos Group since 2020. The Kymos Group is a leading international CRO providing analytical and bioanalytical services to support drug development from preclinical stages to market authorization.
About Prolytic / Kymos GroupTo strengthen our Quality Assurance team, we are looking for a motivated QA Specialist (m/f/d) to join us at the earliest possible date.
Your Responsibilities- Maintenance and continuous improvement of the GLP quality system
- QA review and approval of study plans, raw data, and final study reports
- Handling of deviations, OOS/OOT investigations, and follow-up of CAPAs
- Preparation, review, and maintenance of SOPs and quality-relevant documentation
- Planning, conduct, and follow-up of internal audits and of customer and regulatory inspections
- Training of staff in GLP and QA-related topics
- Close collaboration with bioanalytical departments and the QA teams within the Kymos Group
- A responsible and varied position in an established GLP-certified bioanalytical laboratory
- Integration into an international CRO group with development and career opportunities
- Opportunity to work on innovative drug development programs for international biotech and pharma clients
- Flat hierarchies and short decision-making processes
- A collaborative and scientifically driven working environment
- Flexible Working hours / flextime
- Good accessibility by car and public transportation
- Free drinks (coffee, tea, water)
- Company medical care
- Competitive salary and benefits package
We look forward to receiving your application and getting to know you.
Your Profile- University degree in a life science discipline (e.g. Biology, Chemistry, Biochemistry) or a comparable qualification
- Professional experience in Quality Assurance within GLP and sound knowledge of GLP regulations
- Knowledge of GMP-regulations desirable
- Structured, detail-oriented, and independent working style
- Strong communication skills and a collaborative mindset
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