Senior Manufacturing Engineer
Content + Source + Freshness • 16 Dec 2025 • 95% confidence
Offer value
Strong offer due to the specialized nature of the role in a regulated industry, competitive salary, and clear advancement opportunities.
- Competitive salary in a leading medical device company
- Strong career growth potential in a regulated environment
- Hands-on role focusing on equipment and quality
Pros
- Opportunity to work in a leading medical device facility
- High attention to detail required, promoting professional quality skills
- Fully onsite role allows for direct collaboration with teams
Cons
- Onsite nature may limit flexibility for some candidates
- Requires specific experience in regulated environments
- Potentially high-pressure environment during equipment validation
Who it's for
Mid-Senior • Onsite
Good fit
- Experienced manufacturing engineers
- Detail-oriented engineers in medical device sectors
- Professionals looking to enhance compliance experience
Not recommended for
- New graduates or candidates with no GMP experience
- Those preferring remote or hybrid work arrangements
- Professionals uninterested in documentation-heavy roles
Motivation fit
Key skills
About the job
We are seeking a skilled Senior Manufacturing Engineer to join a high-performing team at a leading medical device manufacturing facility. This role will focus primarily on equipment revalidations and machine relocations, involving both hands-on technical work and comprehensive documentation responsibilities. This role is ideal for someone with strong attention to detail, excellent planning skills, and a solid background in regulated manufacturing environments. The role is fully onsite.
Key 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
- Leverage prior experience in authoring technical and validation documents
- Proactively resolve issues and ensure smooth execution of revalidation processes
Equipment Scope May Include:
- CNC machines
- Coating machines
- Packaging equipment
- Utility panels
- Other production and manufacturing assets
Ideal Candidate Profile:
- 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
