Head of MS&T: Biologics Manufacturing & Tech Transfer

Evotec WD; Toulouse; Sur place; EUR 140 000 - 210 000; Plein temps

Résumé du poste

Sandoz Toulouse seeks a Head of Manufacturing Science & Technology to provide strategic and operational leadership across Process Engineering, Validation, and Technology Transfer. You will drive lifecycle stewardship for manufacturing processes, ensure robust PPQ execution, and lead cross‑functional programs aligned with global quality standards.

The role requires 15+ years in biopharma manufacturing with strong GMP knowledge, and a track record of building high-performing teams in a fast-paced,

Qualifications

• Master’s degree or PhD in Biotechnology, Biochemical Engineering, Chemical Engineering, Pharmaceutical Sciences, or related discipline.
• 15+ years of experience in biopharmaceutical manufacturing, MS&T, process engineering or technical operations.
• Proven leadership experience managing multidisciplinary technical teams.

Responsabilités

• Own the site process knowledge management strategy and ensure robust lifecycle management of manufacturing processes.
• Oversee validation master planning, PPQ strategy, and data-driven process capability evaluation.
• Lead end-to-end technology transfer for new products and manufacturing processes.
• Develop MS&T organization and foster collaboration across Development, Operations, Quality and Manufacturing.
• Ensure GMP, HSE and corporate policy compliance and support regulatory inspections.

Connaissances

Leadership

Multidisciplinary teams

GMP expertise

Data-driven decision making

Formation

Master’s or PhD in Biotechnology/Engineering

Outils

Process Validation Tools

Technology Transfer Tools

Description du poste

Sandoz Toulouse seeks a Head of Manufacturing Science & Technology to provide strategic and operational leadership across Process Engineering, Validation, and Technology Transfer. You will drive lifecycle stewardship for manufacturing processes, ensure robust PPQ execution, and lead cross‑functional programs aligned with global quality standards.

The role requires 15+ years in biopharma manufacturing with strong GMP knowledge, and a track record of building high-performing teams in a fast-paced,