Careers at TRB

Build a meaningful career in a company that grows with you.

Person in protective gear operating a sterilization machine in a lab

A person in a lab coat and hairnet working inside a laboratory room.

Hands holding a syringe in a medical setting with labels in the background.

Person working at a desk with computer monitors in an office setting

What we offer

For more than 45 years, TRB has constantly developed and deepened its expertise in all areas of the pharmaceutical industry to distribute and sell its ophthalmic, muskuloskeletal, orthopaedics and neurological products. TRB is a family-owned company committed to long-term development, for our people and for the organisation.

Our structure remains deliberately human-sized, enabling short decision paths, strong collaboration, and meaningful ownership. We promote autonomy and accountability, giving employees the opportunity to broaden their scope, take on diverse responsibilities, and contribute to cross-functional initiatives. This environment supports continuous learning and sustainable career growth over time.

Open roles

TRB regularly offers development opportunities for apprentices, students and graduates, as well as experienced professionals. We offer long-term career opportunities in many fields, both in Switzerland and with our subsidiaries abroad. Our open roles are always shared on our website and on LinkedIn, we invite you to follow us and check back regularly.

We appreciate your interest in TRB, and to keep the process smooth for everyone, we only consider applications linked to published openings, any new opportunity will be clearly posted online.

Careers Listing Heading

01 May 2026

Metrology Specialist

Production

TRB is recruiting a Metrology Specialist at 80–100% on a permanent contract for its pharmaceutical site in Vouvry.

Research & discovery

Early research is often conducted through internal expertise and collaborations with academic or industry partners. Work typically includes target and disease biology, molecule selection, lead optimisation, preclinical evaluation, and early formulation feasibility.

Clinical development

Clinical development generally covers study strategy and protocol design, ethics and operational set-up, site activation and patient recruitment, support of Phase I–III programmes, data analysis and reporting, and continuous safety monitoring.

Regulatory approval

Regulatory activities span strategy and scientific advice, compilation of quality and clinical documentation, submission and review support, responses to authority questions, inspection readiness, and ongoing maintenance of approvals and updates.

Industrialisation & manufacturing

Industrialisation and manufacturing include process development and scale-up, technology transfer and validation, GMP production with in-process controls, quality control testing and batch release, stability and packaging activities, continuous process improvement, and supply planning with distribution coordination.

Launch & commercialisation

Launch and commercialisation typically involve access and launch preparation, medical affairs and education, responsible scientific communication, stakeholder engagement, and lifecycle management activities over time.

Cross-functional

Quality assurance provides systems and oversight across stages. Pharmacovigilance supports patient safety post-launch. Legal, compliance and governance guide risk management and decision-making. Finance, IT and Human Resources are key enablers behind the scenes, helping our teams perform at their best through reliable operations, modern tools and a supportive work environment.