Thermo Fisher Scientific is seeking a Requalification Technician for its Covingham, UK facility, focusing on maintaining validated sterile fill/finish processes in a GMP-regulated environment. The role involves executing requalification activities, supporting regulatory compliance, and ensuring operational readiness
Job Summary
This position focuses on maintaining the validated state of sterile fill/finish processes and supporting systems.
You’ll be responsible for executing and managing process requalification activities, ensuring continued compliance with EU Annex 1, GMP standards, and site contamination control strategies.
Join a global Pharma Services organisation supporting the development and manufacture of life-saving therapies.
Matching Summary
Match Score: 85
Thermo Fisher Scientific is seeking a Requalification Technician for its Covingham, UK facility, focusing on maintaining validated sterile fill/finish processes in a GMP-regulated environment. The role involves executing requalification activities, supporting regulatory compliance, and ensuring operational readiness.
Skills & Requirements
Must-have
sterile fill/finish processes
process requalification activities
GMP standards
temperature-controlled systems requalification
cleanroom environments
Nice-to-have
support operational readiness
contribute to high standards
structured, detail-oriented approach
Key Requirements
Degree or equivalent in engineering, pharmaceutical sciences, biotechnology
Experience in validation, requalification, or process qualification within a GMP-regulated pharmaceutical or biotechnology manufacturing environment
Background in sterile or aseptic manufacturing is strongly preferred
Good understanding of cGMP, data integrity, and regulatory expectations