- Localisation : Basel, Basel-City Switzerland
- Poste : We are growing : Join us as a GMP expert
- Sector: Life Science
- Type de contrat : Permanent
- Date de démarrage : ASAP
Agap2 is a European engineering and operational consulting group founded in 2005 and specialized in industry. We operate in the Pharmaceutical, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.
As a consultant, you will support our clients in the successful execution of their projects by providing your technical expertise and engineering know-how.
You are adaptable, proactive, and motivated to work in diverse industrial environments, contributing to high-impact engineering projects for leading international companies.
Vos missions principales sont :
At AGAP2 Switzerland, you’ll support varied GMP projects for leading pharma, biotech and medtech companies—while building a long-term career with one permanent employer.
Depending on your expertise, you may work across engineering, qualification, validation, quality, laboratories, maintenance or operational excellence. You’ll tackle technical challenges, collaborate with client and AGAP2 teams, contribute to project documentation and improvement activities, and grow through exposure to different technologies and environments.
Your potential areas of expertise
- Engineering: process, mechanical, electrical, automation, facilities, equipment, clean and black utilities
- Qualification & Validation: FAT/SAT, commissioning, IQ/OQ/PQ, equipment, process, cleaning, CIP/SIP and utilities validation
- Quality Assurance: GMP quality systems, deviations, CAPA, change control, audits, batch records and validation QA
- Laboratories: QC operations, LIMS, analytical methods, laboratory equipment and data integrity
- Operational Excellence: Lean management, process improvement, root cause analysis and performance optimization
- Maintenance: preventive and corrective maintenance, CMMS, reliability and troubleshooting
Your assignments may cover different project phases, from design and implementation to qualification, start-up, production, and continuous improvement.
Ce poste est fait pour vous si...
- Degree in engineering, life sciences, chemistry, biotechnology, pharmacy, or a related field.
- Professional experience in a GMP-regulated environment.
- Experience in at least one of the following areas: engineering, CQV, QA, QC, laboratories, maintenance, manufacturing, or operational excellence.
- Structured, autonomous, and solution-oriented mindset.
- Strong communication skills and a willingness to work in varied environments.
- Fluent in English and in German.
Nous rejoindre, c’est...
-
- Joining a group with strong development potential that aims to improve your employability on challenging and varied projects.
- Joining a structure that has been established in Switzerland for a long time with a client portfolio that includes leaders in the sector.
- Having a sustainable job with stability and access to a real collaboration.
- Benefit from training with accredited and certified centers.
- Having a local management team to support you in the achievement of your missions and in the development of your career.
- Being part of a dynamic, committed team with real human values that we live by every day.
Only applications from Swiss and EU citizens will be considered. Please note that due to Brexit we are no longer accepting applications from the UK.