Quality Assurance Specialist

• 20 October 2026
• 80 - 100%
• Indefinite duration
• English (Intermediate), French (Fluent)
• Chemin Saint-Marc 3, 1896 Vouvry
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Quality Assurance Specialist ###

A pharmaceutical laboratory active in the fields of pharmacy and biotechnology is recruiting for the Quality Assurance Department a Quality Assurance Specialist at 80%, for an indefinite duration.

TRB Chemedica, an international Swiss pharmaceutical group, active in more than 60 countries, has been a major player for 40 years in the production and distribution of reference therapies for the treatment of ophthalmological, rheumatological and neurological conditions. As a human-sized company, TRB develops a culture where autonomy, trust and creativity constitute a true foundation for professional fulfillment. The project-based work organization allows talents to develop cross-functional skills, thus promoting versatility and internal promotion.

The Vouvry site specializes in the production of rheumatological injectables and a neurological active ingredient. It meets the highest requirements, notably through its GMP and ISO 13485 certification.

Your mission :

Rattaché·e to the Quality Assurance Manager, you play a key role in the maintenance, monitoring and improvement of our Quality Management System within our pharmaceutical site.

As a true quality system referent, you ensure the continuous improvement of quality processes, in order to guarantee their compliance with current regulatory requirements, while actively contributing to the performance of the quality system.

In this capacity, you ensure the management of several key processes, notably Non-Conformities (NC), Corrective and Preventive Actions (CAPA), Change Controls (CC), Risk management as well as Internal Audits. You ensure their effectiveness, respect for deadlines and the relevance of associated performance indicators.

Thanks to your quality expertise and your mastery of electronic document and quality management tools, you actively participate in the modeling and optimization of workflows in the electronic eQMS system Ennov in order to support users and improve process efficiency.

You ensure the monitoring of quality indicators (KPI), the analysis of process performance, the preparation of quality reviews as well as the maintenance of associated documentation. You also participate in quality activities related to the review of batch records in the release process.

Finally, you ensure a back-up role for several strategic quality processes, notably document management, training management as well as supplier management.

Your profile :

Education and experience

• Higher scientific education (Bachelor, Master, Engineer, Pharmacist or training deemed equivalent).
• Experience in Quality Assurance preferably in a pharmaceutical, biotechnological or medical devices environment.
• Significant experience in the management of quality systems.
• Knowledge of GMP/BPF frameworks and/or the ISO 13485 / ISO 9001 standard.

Technical skills

• Knowledge of systems: Non-Conformities (NC - Deviations) - CAPA - Change Control (CC) - Quality risk management - Internal audits
• Recommended experience in the administration and use of electronic quality management systems (eQMS).
• Demonstrate interest in modeling and optimizing quality workflows in an electronic environment.
• Experience in the implementation and monitoring of quality indicators (KPI).
• Mastery of office tools and aptitude for data analysis.

Personal skills

• Interpersonal ease and ability to collaborate with various interlocutors.
• Autonomy and sense of responsibility.
• Spirit of initiative and ability to propose solutions.
• Proactivity and ability to identify improvement opportunities.
• Excellent analytical and risk management skills.
• Rigor, sense of organization and priority management.
• Ability to manage several activities in parallel and respect deadlines.
• Very good writing skills.

Languages

• Fluent French.
• Good level of professional English, both written and oral.

Start date: immediately or to be agreed

Our proposal :

Joining TRB Chemedica SA means the assurance of benefiting from:

• The welcoming reception of a competent and dynamic team, committed to promoting personal development.
• First-class social benefits (Pension fund, sickness and accident loss of earnings insurance).
• A 13th month salary, a minimum of 25 days of vacation per year as well as days offered in addition to the official public holidays of the canton of Valais
• Free parking, preferential rates for meals
• Advantages offered by partners in the region
• We invite you to send us your complete application file (CV, cover letter, work certificates and diplomas).

Find our vacancies on our website: https://www.trbchemedica.com/careers/