QA Specialists GMP (x5 all levels) - near Lucerne, Switzerland (FTC)
Clintec is actively recruiting for five temporary Quality Assurance Specialists to join our expanding global company in Switzerland. The positions are site-based with our global biotech client based in Schachen, near Lucerne, on a full-time, fixed term basis until the end of June 2018 (with a strong likelyhood of extension).
The QA Specialists will provide ongoing support to our clients Quality Assurance team and will assist with a backlog of work in the department.
Responsibilities of the QA Specialist:
Review of documents for final disposition (final release) of clinical supplies to clinics, including label release, GMP batch record review for packaging activities, regulatory review for compliance against filings.
Query TrackWise for deviations and changes
Utilize SAP Inventory Management system
Track and report Metrics related to disposition activities
Support other QA members when necessary
Educated to Bachelor Degree specialising in Pharmaceutical Science (Biology/Chemistry Preferred) or equivalent
Sound understanding of pharmaceutical GMP behaviors and Quality Assurance
Previous experience in a similar type/level role
Systematic and thorough approach to work
Ability to work collaboratively with site operations
Ability to prioritize and handle a high workload
Practical approach, team player and flexible
Fluency in English and German languages (both written and spoken)
Willingness and ability to be site-based in Schachen
Clintec is a dynamic, UK headquartered, privately owned, full service Contract Research Organisation with a presence in over 50 countries worldwide. We have been providing clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries and assisting in their key product development efforts for over two decades. At Clintec we have experience in managing clinical trials in all major therapeutic areas including oncology, rare disease, neurology, cardiovascular, psychiatry, infectious disease, rheumatology, immunology, respiratory and gastroenterology.
Clintec employees can expect to receive expert training and guidance throughout their careers as well as the opportunity to be involved in every aspect of Clinical Trials across the full life-cycle of the drug development process from the CRO perspective. We have strong partnerships with some of the world's leading pharmaceutical companies and employees can expect to be involved in some of the most prestigious drug development projects with the opportunity to develop, progress and travel globally. Clintec offers a competitive salary and rewards package.