Staff Validation Engineer, Process and Cleaning
Role Overview
How will you make an impact?
The Staff Engineer, Process and Cleaning Validation supports Thermo Fisher’s mission by ensuring manufacturing processes and cleaning procedures are validated, compliant, and capable of consistently delivering high-quality products in a sterile/aseptic environment.
What will you do?
• Lead process validation (PPQ) and cleaning validation activities
• Develop validation strategies for new and existing products and processes
• Author and execute validation protocols and reports
• Perform data analysis to support validation conclusions
• Support change controls, deviations, and CAPAs
• Collaborate with Manufacturing, Quality, and MS&T teams
• Ensure alignment with cGMP and regulatory expectations
• Support internal and external audits and inspections
How will you get here?
Full Job Posting
Work Schedule
- Environmental Conditions
- Job Description
- How will you make an impact?
- The Staff Engineer, Process and Cleaning Validation supports Thermo Fisher’s mission by ensuring manufacturing processes and cleaning procedures are validated, compliant, and capable of consistently delivering high-quality products in a sterile/aseptic environment.
- What will you do?
- Lead process validation (PPQ) and cleaning validation activities
- Develop validation strategies for new and existing products and processes
- Author and execute validation protocols and reports
- Perform data analysis to support validation conclusions
- Support change controls, deviations, and CAPAs
- Collaborate with Manufacturing, Quality, and MS&T teams
- Ensure alignment with cGMP and regulatory expectations
- Support internal and external audits and inspections
- How will you get here?
- Education:
- Bachelor’s degree in Engineering, Chemistry, Life Sciences, or related field
- Experience:
- 8+ years of experience in process and/or cleaning validation
- Experience in sterile/aseptic manufacturing environments (required)
- Strong knowledge of cleaning validation, including residue limits and risk-based approaches
- Experience with lifecycle validation and PPQ
- Knowledge, Skills, Abilities:
- Strong understanding of cGMP and regulatory requirements
- Data analysis and problem-solving skills
- Technical writing and documentation expertise
- Ability to manage multiple projects and priorities
- Strong cross-functional collaboration skills
Qualifications
- 8+ years of experience in process and/or cleaning validation
- Experience in sterile/aseptic manufacturing environments (required)
- Strong knowledge of cleaning validation, including residue limits and risk-based approaches
- Experience with lifecycle validation and PPQ
- Strong understanding of cGMP and regulatory requirements
- Data analysis and problem-solving skills
- Technical writing and documentation expertise
- Ability to manage multiple projects and priorities
- Strong cross-functional collaboration skills
About Thermo Fisher Scientific
The world leader in serving science.
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