Job Title: Senior Manufacturing Engineer
We are seeking a skilled and experienced manufacturing engineer to lead our equipment revalidation efforts and relocate machinery within a regulated medical device manufacturing facility.
The ideal candidate will have strong technical knowledge, excellent planning skills, and a solid background in regulated manufacturing environments.
This role involves hands-on technical work, comprehensive documentation responsibilities, and collaborating with cross-functional teams to ensure compliance with internal validation procedures and regulatory standards.
Main Responsibilities:
* Lead and support revalidation efforts for production equipment
* Develop and execute relocation protocols for a range of machinery
* Create and maintain detailed IQ documentation using existing templates
* Participate in and support equipment moves within the facility
* Ensure compliance with internal validation procedures and regulatory standards
* Collaborate with cross-functional teams to complete documentation efficiently and accurately
About You:
* Degree-qualified in Engineering (Level 7 minimum; Level 8 preferred)
* Proven experience in equipment validation, revalidation, and technical documentation
* Strong background in authoring validation and commissioning documentation
* Solid understanding of GMP requirements in medical device or similarly regulated industries
* Detail-oriented, organized, and capable of independently driving documentation through to completion
* Strong communication skills and ability to work within a small, focused team