Staff Validation Engineer, Process and Cleaning

Work Schedule

First Shift (Days)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

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