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
agap2 - HIQ ConsultingEngineering Consulting in the fields of Life Science, Automation, Energy, Railway, Construction with Offices in Zürich, Basel und Lausanne
