This position is a newly created role.
You will have the opportunity to contribute to the development of new products and the improvement of existing processes.
You will report to the Operations Supervisor and carry out production operations in accordance with defined operating procedures and in compliance with production constraints and QHSE rules defined by the company.
These operations take place in a controlled atmosphere and are covered by training provided by the employer.
The variety of this position requires rigor, organization, and autonomy.
You have a 2-3 year degree in process engineering, biological engineering, biotechnology, or equivalent, with 3 to 5 years of experience in production, preferably in the pharmaceutical industry or as a manufacturer of active ingredients.
You have initial professional experience in a regulated environment (GMP).
Additional knowledge of microorganism fermentation/purification (filtration, precipitation) and microbiology would be desirable.
You are proficient in Microsoft Office (Word and Excel).
You can read and write French (drafting and reading documents).
Hours: shift work
Our young company covers 50% of health insurance costs and 100% of pension costs. We regularly organize internal events to develop team cohesion. A genuine corporate culture based on a human and professional approach.