MSAT Process & Validation Expert (Fixed-term contract)

Responsibilities

• Support process validation and support lifecycle maintenance of process to ensure manufacturing processes are capable of consistently producing high quality products.
• Execute and oversee cleaning validation activities to verify process effectiveness and prevent the risk of cross‑contamination.
• Monitor critical process parameters (CPPs) and manufacturing process parameters (MPPs) through Continued Process Verification (CPV) and Cleaning Verification (CV) activities.
• Analyze process data and trends to identify variations, propose corrective actions and drive continuous improvement projects aimed at reducing variability and optimizing yield and quality.
• Support technology transfers, equipment qualifications and Extractables & Leachables (E&L) assessments to ensure process requirements are correctly transferred and validated.
• Participate in and support internal and external audits within your area of expertise, contributing to the maintenance of compliance with regulations and GSK standards.
• Take on the responsibilities associated with your role by focusing on site objectives, contribute to creating an environment of accountability by encouraging collaboration, individual commitment, and providing meaningful contributions to achieving company goals aligned with GSK culture.
• Why you?
• Basic Qualifications & Skills
• We are looking for professionals with these required skills to achieve our goals:
• University degree in a relevant scientific discipline (e.g. Pharmacy, Pharmaceutical Chemistry and Technologies, Chemistry, Engineering, Biology etc).
• Experience in production processes or the pharmaceutical sector is appreciated.
• Excellent proficiency in using computer software and digital tools for the execution of production and management activities.
• Good knowledge of written and spoken English.
• Ability to work in a team, skills in promoting collaboration and resolving conflicts within the group.
• Preferred Qualifications & Skills
• If you have the following characteristics, it would be a plus:
• Results-oriented mindset and continuous improvement: Constant commitment to achieving business and quality objectives

Benefits

Additional Information

We manufacture and supply reliable, high-quality medicines and vaccines to meet patients' needs and drive our performance. Our network of 37 medicines and vaccines manufacturing sites delivered 1.7 billion packs of medicines and 409 million vaccine doses in 2024 to help make a positive impact on the health of millions of people. Our supply chain is not just core to our operations; it's vital to bringing our innovations to patients as quickly, efficiently and effectively as possible. Technology is transforming how we manufacture medicines and vaccines, enabling us to increase the speed, quality and scale of product supply. We need the very best minds and capability to help us on our journey to make more complex products, harnessing the power of smart manufacturing technologies including robotics, digital solutions and artificial intelligence to deliver for patients. Job title: MSAT Process & Validation Expert Location : Rosia, Italy Employment type: Fixed-term (until 15 December 2026) Closing date for applications: 14 June 2026 Position Summary The role ensures the validation, optimization and maintenance of robust manufacturing processes, supporting new product introductions, technology transfers and the validation lifecycle. The role contributes to improving efficiency, consistency and compliance with Site, GSK and Regulatory requirements, ensuring the production of safe, effective and cost‑efficient products. The role operates by planning, executing and documenting validation, monitoring and continuous improvement activities in collaboration with Operations, Quality and Engineering functions. The skills required for the role are highlighted through the specific training matrix assigned to each employee based on the work requirements defined by the manager.

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