
Advanced Manufacturing Specialist
3 days ago
We are seeking a skilled Manufacturing Professional to join our high-performing team at a leading medical device manufacturing facility.
Key Responsibilities
- Evaluate and validate production equipment
- Develop relocation protocols for machinery
- Create detailed documentation using existing templates
- Participate in equipment moves within the facility
- Ensure compliance with internal validation procedures and regulatory standards
- Collaborate with cross-functional teams to complete documentation efficiently
- Leverage prior experience in authoring technical documents
Equipment Scope May Include
- CNC machines
- Coating machines
- Packaging equipment
- Utility panels
- Other production 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 authorizing validation and commissioning documentation
- Solid understanding of GMP requirements in medical device or regulated industries
- Detail-oriented, organized, and capable of driving documentation to completion
- Strong communication skills and ability to work within a small team
Seniority level
- Mid-Senior level
Employment type
- Contract
Job function
- Engineering and Quality Assurance
Industries
- Medical Equipment Manufacturing
GMP Requirements: Medical Device Industries, Regulations, Compliance
Document Creation: Technical Documents, Validation Reports, Commissioning Documentation
Mechanical Knowledge: CNC Machines, Coating Machines, Packaging Equipment, Utility Panels, Other Production Assets
Why this role?
This is an excellent opportunity for an experienced Manufacturing Professional to take on a challenging role in a high-performing team. The ideal candidate will have strong technical knowledge, excellent communication skills, and the ability to work independently.
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