QC Scientist

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