You will be responsible for leading projects to transfer pharmaceutical manufacturing processes between sites (R&D to production, site-to-site, subcontractors), in compliance with regulatory standards (GMP), deadlines, quality, costs and customer requirements.

Your key responsibilities will be as follows:

• Coordinate and manage all stages of an industrial transfer project (from feasibility to production start-up).

• Analyse process data to be transferred and identify critical points.

• Define the transfer plan and validation strategies (IQ/OQ/PQ, validation batches, etc.).

• Organise and monitor industrial trials (process validation, etc.).

• Act as the interface between technical, quality, production, R&D, regulatory affairs, purchasing teams, etc.

• Participate in writing and reviewing technical documentation (protocols, validation reports, change control, etc.).

• Manage relationships with external partners (CDMOs, equipment suppliers, laboratories, etc.).

• Ensure compliance with GMP and current regulatory requirements.

• Monitor performance indicators (cost, quality, deadline) and report to management.

Profile required:

With a Master's degree (Engineering, Master's specialising in industrial pharmacy, process engineering, biotechnology, chemistry...), you have at least 3 to 5 years of experience in the pharmaceutical industry in similar roles (transfer, industrialisation, production, etc.).

Technical skills:

• With a solid foundation in pharmaceutical processes (dry, sterile, biotech, etc. forms), validation, qualification and quality documentation

• Mastery of GMP regulatory standards

• Ability to manage multiple projects in parallel

• Professional English (written and spoken).

Personal skills:

• Organisational skills,

• Rigour, analytical skills, good interpersonal skills and autonomy.