Global Senior Pharma Process Manager MS&T – Pharmaceutical Company

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/80ks66

Introduction:

Chaberton Professionals , the division of Chaberton Partners dedicated to the search and selection of Middle Management profiles, is currently looking for a Global Senior Pharma Process Manager MS&T; for an important pharmaceutical group based in Florence.

The role acts as a strategic technical bridge between R&D;, Manufacturing, Quality, Regulatory Affairs, Supply Chain, and CMOs. The primary mission is to lead industrialization, process optimization, and technology transfer programs to ensure robust, scalable, and compliant manufacturing processes across the product lifecycle.

:

- Assess process scalability, manufacturability and operational robustness in industrialization and technology transfer activities.
- Identify and evaluate CPPs, CQAs and process-related risks impacting product quality, reliability and supply continuity.
- Partner with the MS&T; Lead and cross-functional stakeholders to evaluate manufacturing strategies, balancing quality, compliance, timing, cost and operational efficiency.
- Escalate technical and operational issues when appropriate, with data-driven analyses and recommendations.
- Coordinate Production, QA, QC, Regulatory Affairs, Engineering, Supply Chain and external CMOs during industrialization and technology transfer projects.
- Support project planning and execution, aligning timelines, priorities, risks and resources across stakeholders and manufacturing sites.
- Act as primary technical contact for assigned projects, facilitating communication, resolving issues and streamlining decision-making.
- Report project status, risks and technical challenges to MS&T; leadership.




- Support investigations of process deviations, variability and performance optimization.
- Drive continuous improvement initiatives to enhance process robustness and efficiency.

Requirements:

- Master’s Degree in CTF, Chemistry, Pharmacy or Chemical/Process Engineering.
- 10–15 years of experience in pharmaceutical manufacturing, MS&T;, industrialization, process engineering or technology transfer.
- Strong, proven exposure to solid dosage manufacturing, plus experience in other pharmaceutical forms such as steriles.
- Direct involvement in industrial scale-up, process validation and process troubleshooting.
- Deep understanding of pharmaceutical manufacturing processes and industrial scale-up principles.
- Solid knowledge of GMP, process validation regulations and technology transfer guidelines.
- Ability to analyze process data, variability and CPPs.
- Advanced problem-solving and investigation methods (Root Cause Analysis, Fishbone, 5 Whys, FMEA) to support deviations and troubleshooting.
- Strong project and stakeholder management in cross-functional, international environments.
- Excellent problem solving with a structured, risk-based approach.
- Strong communication and influencing skills with technical and non-technical stakeholders.
- High adaptability in complex, dynamic industrial environments.
- Ability to balance technical, quality, regulatory and operational priorities.

Contract & Compensation :

- CCNL Chimico Farmaceutico
- Salary range between € 55.000 and 65.000 + Bonus.

Location: Florence - 2 days of lavoro da remoto. Travel up to 50%.

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/80ks66