Associate Scientist QC Release
vor 2 Wochen
Caring for the world, one person at a time... inspires and unites the people of Johnson & Johnson. We embrace research and science - bringing innovative ideas, products and services to advance the health and well-being of people. Employees of the Johnson & Johnson Family of Companies work with partners in health care to touch the lives of over a billion people every day, throughout the world. We have more than 260 operating companies in more than 60 countries employing approximately 135,000 people. Our worldwide headquarters is in New Brunswick, New Jersey, USA.
Janssen Vaccines in Bern (Switzerland) belongs to the Janssen Pharmaceutical Companies of Johnson & Johnson. Janssen is an organization of over 40,000 professionals working passionately to prevent, treat, cure and stop some of the most devastating and complex diseases of our time. In Bern, about 400 people of over 25 nationalities work together with the wider Janssen organization and partners on the development, manufacturing and analytical testing of novel vaccines and bacteria-based pharmaceutical products.
For our site in Bern, we are looking for an open minded, goal driven, motivated Associate Scientist QC Release & Stability.
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
- Comply with all applicable health, safety and environmental regulations, processes and guidelines
Qualifications
- Bachelor or Master's level University/Higher educational degree in a Life Science 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 tasks to plan and deliver according to 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
Randstad Inhouse Services
Frau Sara Ramadani
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