We are seeking a skilled Senior Process 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 equipmentDevelop and execute relocation protocols for a range of machineryCreate and maintain detailed IQ documentation using existing templatesParticipate in and support equipment moves within the facilityEnsure compliance with internal validation procedures and regulatory standardsCollaborate with cross-functional teams to complete documentation efficiently and accuratelyLeverage prior experience in authoring technical and validation documentsProactively resolve issues and ensure smooth execution of revalidation processesIdeal Candidate Profile:Degree-qualified in Engineering (Level 7 minimum; Level 8 preferred)Proven experience in equipment validation, revalidation, and technical documentationStrong background in authoring validation and commissioning documentationSolid understanding of GMP requirements in medical device or similarly regulated industriesDetail-oriented, organized, and capable of independently driving documentation through to completionStrong communication skills and ability to work within a small, focused team