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 Skills: Process Validation Equipment CNC FATs SAT