Head of Manufacturing Science & Technology (all genders)

We’re excited to share this opportunity is part of the Sandoz acquisition of Just-Evotec Biologics in Toulouse. Through this opportunity you will impact the lives of hundreds of millions of people through bold ideas supported by an inclusive, agile company culture. Join us to help make healthcare fairer and faster, help us to pioneer access to medicine! Click to learn more.

Location: Toulouse, France
Type of contract: Permanent

The Head of MS&T is responsible for providing strategic and operational leadership for Manufacturing Science & Technology activities across the site. The role ensures technical oversight of commercial manufacturing processes, validation lifecycle management, and successful execution of technology transfers and new product introductions.
The Head of MS&T acts as the primary technical authority for manufacturing processes and is accountable for maintaining process robustness, product quality, regulatory compliance, continuous improvement, and operational readiness.

The position leads multidisciplinary teams covering Process Engineering, Validation, and Technology Transfer and serves as a key member of the Site Leadership Team.

What You’ll Do:

1. Technical Stewardship & Process Lifecycle Management
Own the site process knowledge management strategy and ensure preservation of critical manufacturing know-how.
Ensure robust lifecycle management of manufacturing processes from commercial launch through discontinuation.
Lead technical assessments of deviations, investigations, root cause analyses, CAPAs, and process-related quality events.
Provide subject matter expertise for upstream, downstream and support manufacturing processes.
Ensure appropriate technical support to manufacturing operations.
Drive continuous process verification and process performance monitoring.
Identify and implement process optimization opportunities to improve quality, yield, reliability, and cost.
2. Validation Stewardship
Own the site validation strategy and validation master planning.
Ensure compliant execution of process validation, cleaning validation and continued process verification activities.
Oversee PPQ strategy, protocol development, execution and reporting.
Ensure statistical trending and data-driven evaluation of process capability
Lead cross-contamination risk assessments and validation activities related to cleaning and decontamination.
Maintain inspection readiness for validation-related topics.
Ensure validation practices comply with global regulatory requirements and internal quality standards.
3. Technology Transfer & New Product Introduction
Lead end-to-end technology transfer activities for new products and manufacturing processes.
Ensure robust transfer of process knowledge from development organizations and external partners
Coordinate technical due diligence, facility fit assessments and gap analyses.
Define and execute Control Strategy implementation including CPPs, CQAs and associated monitoring plans.
Ensure engineering run, PPQ and launch readiness through stage-gate governance.
Drive cross-functional alignment across Development, Operations, Quality, Supply Chain and Engineering.
Support site network expansion and introduction of new technologies and manufacturing platforms.
4. Leadership & Organization Development
Lead and develop the MS&T organization including Process Experts, Validation Engineers and Technology Transfer teams.
Establish a culture of scientific excellence, accountability, innovation and continuous improvement.
Develop organizational capabilities to support future portfolio growth and technology evolution.
Manage workforce planning, succession planning and talent development.
Foster strong collaboration with global MS&T, Development, Quality and Manufacturing organizations.

5. Compliance, Quality & HSE
Ensure all MS&T activities are conducted in compliance with GMP, HSE and corporate policies.
Support regulatory inspections, customer audits and health authority interactions.
Serve as technical representative for process and validation topics during inspections.
Promote a proactive quality culture and risk-based decision making.
Ensure technical risks are identified, assessed and mitigated appropriately.
Who You are:

• Master's degree or PhD in Biotechnology, Biochemical Engineering, Chemical Engineering, Pharmaceutical Sciences, or related scientific discipline.

• 15+ years of experience in biopharmaceutical manufacturing, MS&T, process engineering or technical operations.

• Demonstrated leadership experience managing multidisciplinary technical teams.

• Proven experience in commercial manufacturing support, process validation and technology transfer.

• Strong knowledge of GMP regulations and health authority expectations.

• Experience with biologics manufacturing processes (USP/DSP) preferred.

• Strategic leadership

• Scientific and technical expertise

• Change management

• Cross-functional influence

• Data-driven decision making

• Problem solving and root cause analysis

• Stakeholder management

• Strong communication and coaching skills

Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.

Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!

The future is ours to shape!

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.

FR : Dans le cadre de sa politique Diversité, Evotec étudie, à compétences égales, toutes les candidatures dont celles des personnes en situation de handicap.

ENG : In the frame of our Diversity policy, Evotec considers, with equal competences, all applications including people with disabilities.