GSK
Pharmaceutical
MSATProcess&ValidationExpert(Fixed-termcontract)
Neural analysis suggests this role is
optimal for Mid+ candidates.
“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.
Root cause analysis; Troubleshooting; Risk-based troubleshooting
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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