Life Science consultant : join us as GMP expert

agap2 Switzerland; Bern; On-site; CHF 90,000 - 130,000; Full time

Job summary

AGAP2 Switzerland is seeking engineers and quality professionals to support diverse GMP projects for life science clients. You will work across engineering, qualification, validation, QA, QC, laboratories, maintenance or operational excellence, collaborating with client and AGAP2 teams to drive project documentation and improvements.

The role offers exposure to multiple technologies and environments, with a pathway to long-term career growth within a single employer in Switzerland.

Qualifications

• Experience in a GMP-regulated environment.
• Ability to work across engineering, CQV, QA, QC, laboratories, maintenance or operational excellence.
• Strong communication skills and the willingness to work in varied environments.

Responsibilities

• Support GMP projects for pharma, biotech and medtech clients.
• Collaborate with client and AGAP2 teams and contribute to project documentation.
• Engage in qualification, validation and continuous improvement activities.
• Grow through exposure to different technologies and project phases.

Skills

GMP experience

Cross-functional

Communication

Bilingual EN/DE

Education

Engineering / Life Sciences degree

Tools

LIMS

CMMS

Job description

One permanent employer. Multiple technical challenges.

Are you an engineer or quality professional with experience in a GMP environment?

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.

What we are looking for

• 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.

Why AGAP2?

• Permanent contract with AGAP2 Switzerland.
• Projects with leading Life Science companies.
• Technical diversity without sacrificing stability.
• Career development based on your expertise and ambitions.
• A community of engineers and quality professionals across Switzerland.
• The opportunity to contribute to the Life Science hub from within.

Ready to turn your GMP experience into a broader technical journey? Join AGAP2.