Qc Scientist
vor 2 Wochen
Scientist QC
**Your Tasks**:
- Analytical Method Lifecycle
- Lead and execute project tasks related to method development, implementation, transfer, and validation.
- Prepare and maintain test instructions, analytical methods, study plans, and technical reports according to internal quality standards.
Data Review & Documentation
- Perform double-check and release of raw data and analytical results in LIMS.
- Ensure data integrity and compliance in accordance with ISO and GMP requirements.
Laboratory Support
- Provide expert technical support to the QC laboratory, including troubleshooting of analytical issues.
- Independently plan, execute, evaluate, and document assigned tasks and projects.
Quality & Compliance
- Manage and support Change Requests (CRs), Deviations (DRs), investigations (SST, OOX, etc.) and CAPAs.
- Ensure full adherence to quality, safety, ISO, and GMP standards in all work processes.
**Your Profile**:
Education
- PhD in Biotechnology, Biochemistry, Pharmaceuticals, or a related field
- 1 year of relevant experience preferred (entry-level considered)
- or MSc in a relevant scientific field
- Minimum 2 years of relevant experience required (laboratory or scientist roles)
Technical Skills
- Hands-on experience with ELISA (focus on relative potency)
- Hands-on experience with qPCR, including method development and/or validation
- Data Review experience is important and strongly preferred
- GMP experience is a plus
Other Requirements
- Strong understanding of laboratory best practices and data integrity principles
- Ability to work both independently and collaboratively in cross-functional environments
- Excellent communication skills, with English mandatory; German is an advantage
- Ability to work on-site with a maximum of 2 remote days per week
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