Production Director

Location:Vouvry (Chablais, Canton of Valais) About UsTRB Chemedica SA is an international Swiss pharmaceutical group operating in more than 60 countries. For over 40 years, we have been a major player in the production and distribution of reference therapies for ophthalmological, rheumatological and neurological disorders. Our Vouvry site employs around 100 professionals and fosters a culture built on autonomy, trust and creativity—providing solid foundation for professional fulfilment. Work is organised on a project basis, enabling talent to develop cross-functional skills and promoting versatility and internal mobility. Specialised in the production of injectables and neurological active pharmaceutical ingredients (APIs), the site meets the highest standards, holding GMP and ISO 13485 certifications. Ideally located just a few kilometers from Lake Geneva and the Portes du Soleil ski area, it offers an exceptional working environment. Due to an upcoming retirement, we are seeking our future

• Production Director (M/F)to join the site’s leadership team. Your

MISSIONS

As Production Director, you will play a pivotal role in ensuring the availability of high-quality injectable hyaluronic acid products. As a member of the site’s Management Committee, you will contribute to defining and steering the industrial strategy, driving operational performance and embedding operational excellence. You will have full responsibility for production activities and related industrial functions in a demanding and highly regulated environment. Your leadership will foster sustainable performance, talent development and a strong Quality culture. Scope of the Role

• The current scope includes:An extractive chemistry unitA prefilled hyaluronic acid syringe production unit
• The logistic sector
• Depending on candidate profiles, this scope may be adjusted. The core focus is still the production of prefilled syringes. Key Responsibilities
• Operational and Strategic Leadership
• Oversee production to meet QQCDSE standards (Quantity, Quality, Cost, Delivery, Safety, Environment). Define and implement the site’s production strategy in alignment with Group goals. Drive operational excellence initiatives (Lean, Six Sigma, OPEX) to enhance quality, productivity, process robustness and profitability. Contribute to the industrial master plan, capacity planning and transformation projects. Leadership and Organizational Management
• Lead and develop the industrial organization, with a strong emphasis on coaching and empowering management teams. Build team capability, engagement and performance, fostering a culture of accountability and continuous improvement. Quality, Compliance and Risk Management
• Play a key role in strengthening the site’s Quality culture, working closely with the Quality Director, Technical Director and their teams. Ensure compliance with all regulatory

REQUIREMENTS

within your scope. Actively manage deviations and investigations (CAPA, non-conformities). Anticipate and prepare for regulatory inspections. Research & Development

• Maintain regular interactions with the Group’s R&D departments to support innovation and industrialization. Financial Management and Investments
• Manage the production budget and optimise allocation of human, technical and financial resources. Participate in industrial investment projects, including equipment acquisition and facility modernization or expansion. Health, Safety and Environment
• Demonstrate exemplary behavior in occupational health and safety. Support initiatives to reduce the environmental impact of industrial activities, in line with EHS commitments.

YOUR PROFILE

Industrial pharmacist or engineer by training (Master’s or PhD in chemistry, biotechnology, production or equivalent). Minimum 15 years’ experience in the pharmaceutical industry, including significant expertise in injectable manufacturing. Ideally, experience in Supply Chain and chemical production, particularly in active pharmaceutical ingredients (APIs). Proven experience in leading industrial organizations, including managing managers. Performance oriented, efficiency and profitability mindset, with a recognized Quality culture. Inspirational leadership, ability to challenge the status quo and drive change. Comfortable operating within a Management Committee and contributing to strategic decisions. Full professional ability in French and English; German is an advantage. Lean Six Sigma certification (Green/Black Belt) or equivalent is a plus. Why Join Us?A strategic leadership role at the heart of the site’s industrial decision-making. The opportunity to fully use your expertise in an environment that values autonomy and innovation. Attractive compensation and first-class working conditions. Industrial investment projects and strong growth momentum. A culture driven by excellence and collaboration. An outstanding geographical location offering quality of life. Our Promise

• Joining TRB Chemedica SA means becoming part of a team of curious minds from diverse backgrounds—committed, motivated professionals with an important level of expertise. You will work in a dynamic production environment with significant investment projects, offering a unique opportunity to have a direct impact on improving patients’ quality of life and shaping the site’s strategic development. Diversity of talent is at the heart of our success. We are looking for bold personalities to build the future with us. Ready to take on this strategic leadership role? Apply today and help shape the future of pharmaceutical excellence.

APPLICATION

deadline: 28 February 2026.