agap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.
As a consultant, you will have to support our clients in the realization of their projects on site by bringing your expertise and your skills.
You are agile and eager to adapt to different work environments that will fuel your curiosity of seeing what’s behind closed doors of the biggest projects of our client’s portfolio.
Tasks
- Reviewing and approving IQOQPQ protocols and reports for a wide range of QC/Production equipments and utilities
- Ensuring compliance with relevant regulations (e.g., GMP, USP, Ph. Eur.).
- Providing technical guidance and support to project teams.
- Participating in equipment qualification meetings and reviews
- Maintaining accurate records and documentation.
- Supporting internal and external audits.
- Staying abreast of relevant industry standards and regulations.
Requirements
- Master's degree in Biotechnology or a related field
- 3 years minimum experience in QA for qualification for pharma, biotech or medtech companies
- Fluent in English
- Swiss or EU nationality
Basel, Switzerland On-site Full-time
agap2 is hiring a QA qualification engineer
About company
At agap2, we are committed to play a part in the projects that will shape our future.
This is why, since 17 years, we support our clients in the success of their projects by providing them with the technical and human expertise of our consultants.
We recruit multi-skilled, high value-added consulting engineers to strengthen the teams of our industrial partners while ensuring that we offer them career opportunities in line with their professional and personal aspirations.
#THINK2MORROW