GSK

Pharmaceutical

MSATProcess&ValidationExpert(Fixed-termcontract)

€55–75k ~AI est. Rosia, Italy FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“MSAT Process & Validation Expert (Fixed-term contract) at GSK. Skills: Process validation, Process optimization, Data analysis, cGMP. Support process validation. Support lifecycle maintenance”

What You'll Achieve.

Ensure manufacturing processes are capable; Ensure consistent production of high quality products; Ensure process effectiveness; Prevent risk of cross-contamination; Ensure Product Control Strategy is in place; Reduce variability; Optimize yield and quality; Ensure process requirements are correctly transferred and validated; Implement effective corrective actions; Implement effective preventive actions; Achieve business objectives; Achieve quality objectives; Optimize activities; Ensure satisfactory results

Industry & Context.

Pharmaceutical
Problems you'll solve

Root cause analysis; Troubleshooting; Risk-based troubleshooting

Eligibility Requirements

Fixed-term contract until 15 December 2026

What They're Looking For.

Must Have

University degree in relevant scientific discipline, Experience in production processes or pharmaceutical sector, Excellent proficiency in computer software and digital tools, Good knowledge of written and spoken English, Ability to work in a team, Skills in promoting collaboration, Skills in resolving conflicts

Nice to Have

Results-oriented mindset, Continuous improvement mindset, Proficient in applied statistics, Proficient in data analysis tools, Technical writing skills

What You'll Do.

Support process validation

Support lifecycle maintenance

Support Continued Process Verification

Support Cleaning Verification

Monitor critical process parameters

Monitor manufacturing process parameters

Analyze process data and trends

Propose corrective actions

Drive continuous improvement projects

Optimize yield and quality

Support technology transfers

Support equipment qualifications

Support Extractables & Leachables assessments

Conduct deviation investigations

Perform root cause analyses

Define corrective actions

Implement preventive actions

Provide technical operational support

Assist with troubleshooting

Assist with management of non-conformities

Participate in internal audits

Support external audits

Focus on site objectives

Contribute to accountability environment

Encourage collaboration

Encourage individual commitment

Provide meaningful contributions

Environment regulations

Apply escalation process

How You'll Work.

Team & Collaboration

Collaboration with Operations; Collaboration with Quality; Collaboration with Engineering; Collaboration within group

Communication Scope

Technical writing; Scientific reports; Investigation documentation; Regulatory documentation

Process & Methodology

Continuous improvement projects

Full Job Description

_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. **Responsibilities** * Support process validation and support lifecycle maintenance of process to ensure manufacturing processes are capable of consistently producing high quality products.

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