Our client, an international pharmaceutical company based in Bern is searching for a Quality Assurance Specialist (GMP Compliance) to assist their Regulatory Compliance team.
- Start date: 14/03/2023 - Duration: Until 31/12/2023 - Extension: possible - Work location: Bern - Hybrid working model: yes - Workload: 80%
- Preparation of GMP documents for regulatory submissions - Attend regulators' questions and audits - Coordinate, perform and follow-up of paper based GMP inspections - Prepare GMP-certificate renewal and tender relevant documentation based on request by Affiliates - Ensure timely implementation of Regulatory Compliance related actions - Support answers to Regulatory Compliance related questions from internal or external stakeholders - Perform Ad-Hoc duties in specialized field - Participate in predetermined trainings
- University degree in natural sciences (e.g. Biology, Chemistry or Pharmacy) - Minimum 3 years of experience in Quality or manufacturing in a pharmaceutical GMP environment - Experienced in reading regulations and with management of Audits - Fluency in German and English skills (written and spoken)
What's on offer?
Our client offers an exciting position in a multi-disciplinary and collaborative environment. Does this description sound like you? If so, please get in touch, and you could be embarking on a new and exciting professional opportunity.
For further information or to apply, please contact Asher Cos, recruiter: firstname.lastname@example.org By applying for this position, I consent to the Swisslinx Group of companies: - storing my personal information (including name, contact details, Identification and CV information etc.) on their internal or external servers for the purpose of informing me of potential employment opportunities - using my personal information or - supplying it to third parties upon express consent for the purpose of informing me of potential job opportunities - transferring where applicable my personal information to a country outside the EEA/EFTA