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Manufacturing and Testing Specialist

Staffingine LLC
North Haven, CT Full Time
POSTED ON 1/19/2025
AVAILABLE BEFORE 4/16/2025

Position : - Manufacturing and Testing Specialist

Location : - North Haven, CT

Job Description

  • We are seeking a highly skilled and motivated Manufacturing and Testing Specialist with experience in the medical devices or hi-tech mechanical / electromechanical product manufacturing industry. The ideal candidate will be responsible for a range of manufacturing and testing activities, ensuring high-quality standards and compliance with industry regulations.

Key Responsibilities :

  • Perform manufacturing, assembly, functional testing, and inspection of parts, sub-assemblies, and final assemblies.
  • Develop, execute, and review protocols related to URS (User Requirements Specification), Design Qualification, FAT (Factory Acceptance Testing), SAT (Site Acceptance Testing), IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification).
  • Generate protocol reports, review and ensure proper approval processes are followed.
  • Ensure compliance with ISO 13485, 21CFR Part 820 regulations (training will be provided if needed).
  • Demonstrate hands-on experience with automation equipment to ensure the efficient production process.
  • Work with vision systems, robots, and inspection systems (preferred but not required).
  • Qualifications :

  • Proven experience in manufacturing, assembly, functional testing, and inspection within the medical devices or high-tech mechanical / electromechanical industry.
  • Expertise in URS, Design Qualification, FAT, SAT, IQ, OQ, PQ processes.
  • Familiarity with ISO 13485 and 21CFR Part 820 (preferred, but not mandatory for candidates with strong industry experience).
  • Hands-on experience with automation equipment is required.
  • Experience working with vision systems, robots, and inspection systems is a plus.
  • Ability to work 100% onsite, with no remote or hybrid options available.
  • Preferred Experience :

  • Strong experience in the medical device industry or equivalent high-tech mechanical / electromechanical product manufacturing environment.
  • Ability to develop and execute protocols on the floor and generate, review, and approve protocol reports.
  • If you meet the qualifications and are excited to join our team, we encourage you to apply. We offer a dynamic work environment and the opportunity to contribute to cutting-edge projects in the medical device manufacturing industry.

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