Associate Scientist Qc Release
Vor 2 Tagen
For our site in Bern, we are looking for an open minded, goal driven, motivated Associate Scientist QC Release & Stability.
QC Release & Stability is involved in the validation and transfer of various test methods and the performance of routine release and stability tests for new materials in the clinical and commercial phase. The chemical methods used internally include chromatographic methods (RP, SEC, IC), TOC, Conductivity and biochemical methods as qPCR, Capillary Electrophoresis, SDS-PAGE, ELISA, Dot Blot etc.
Responsibilities/tasks
- Responsible for performing various chemical and biochemical testing according to internal and/or regulatory standards (EP, USP, ISO, other) for QC testing
- Responsible for release, in-process control and stability testing
- Responsible for performing utility monitoring tests (water-monitoring samples)
- Perform method co-validations, qualification and verifications
- Analyses and reports test results
- Maintain current laboratory equipment and operates analytical and other instruments
- Perform laboratory duties to support department objectives Support the Quality
- Control department in internal and external audits and requests
- Responsible for compliance with Quality goals for this position
- Provide support to analytical development, process development and other stakeholders when the need arises
- Support training and qualifications of team personnel
- Support timely and effective completion of lab events, investigations and CAPAs related to OOS and non-conformances
- Lead and support continuous improvement projects within Quality Control in operational efficiency and GMP compliance Complies with all applicable health, safety and environmental regulations, processes and guidelines
- Provide support to analytical development, process development and other stakeholders when the need arises
Qualifications
- Bachelor or Master's level University/Higher educational degree in a LifeScience discipline
- Familiar with compendial testing and related industry guidelines
- Sound knowledge of analytical laboratory operations and practices
- Work experience in Pharma, Biotech or Vaccines industry is a plus
- GMP experience is a plus
- Self-dependent way of working and taking ownership of assigned task to plan and deliver according agreed timelines
- Demonstrate innovative spirit, strong interpersonal skills and project management abilities
- Ability to work in a dynamic environment according to tight and challenging timelines
- Team player
- Good English and German communication (verbal & written)
This job based in Bern, Switzerland will initially be limited to 12 Months. If you are interested in working with a global leading pharmaceutical company in a dynamic, progressive, and collaborative environment, then send us your application today. Or give us a call if you have any questions
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