Scientist QC Biochemistry Chromatography Lab.

For our client, a pharmaceutical company based in canton Lucerne, we are looking for a Scientist with a strong technical background and hands-on experience in biochemical analytical methods to join the Biologics Analytical Department.

You will be part of a multidisciplinary team and support the development of novel biopharmaceuticals. The Biologics Analytical Department provides support to the manufacturing sites of the company by performing release and stability testing of clinical batches and acting as the interface between method development and validation. We are establishing and validating methods for testing of biologics drug substances and drug products adhering to regulatory GMP requirements.

In this role you will be responsible for the oversight and support of certain quality assurance activities in the space of Quality Operations and Compliance.

General Information:
 

• Start Date: Mid February 2025
• Duration: 12 months contract
• Extension: possible
• Workload: 100%
• Workplace: Schachen, Luzern

Main areas of responsibility include:
 

• Establishing and running chromatography methods for release & stability testing of Biologics.
• Careful documentation of lab work following cGMPs and applying good documentation practices.
• Performing method validation experiments according to approved protocols.
• Authoring of methods and technical protocols and reports.
• Improvement of methods and troubleshooting around equipment and procedures.
• Maintenance and calibration of analytical equipment following cGMPs.

Qualifications:
 

• Master’s degree in Biochemistry/Chemistry/Pharmaceutics/Biological Sciences or similar field
• or Bachelor’s degree/Laboratory Technician EFZ with 3+ years of industry experience.
• Deep knowledge of protein biochemistry and hands on experience with analytical testing by HPLC/UPLC methods, e.g. Size Exclusion, Ion Exchange, Reverse Phase, HIC.
• Detailed knowledge of a relevant CDS (e.g. Empower)
• Ability to pipette small volumes precisely and prepare large number of samples.
• Accurate working and documentation style with adherence to details.
• Analytical method validation and GMP working experience is preferred.
• Strong organizational skills and ability to prioritize.
• Excellent oral and written communication skills in English and German.
• Proven team player, demonstrating mutual respect.