Merrimack Manufacturing

Bachelor's degree in Engineering or related. 2+ years of experience in a regulated industry. Familiarity with GDP & ISO 9000 is preferred

5+ years of experience in medical device manufacturing. QMS knowledge and 21 CFR 820 & ISO 13485 requirements needed. Experience with Minitab, and related software

15+ yrs QMS experience & 10+ yrs in medical device. Bachelor’s degree or equivalent. Experience with ISO 13485/21 CFR 820 & FDA inspections required

3+ yrs experience in quality control of medical devices. Knowledge of 21 CFR 820 and ISO 13485:2016 is required. Bachelor's degree in a related engineering field

4+ yrs experience in technical troubleshooting, strong skills with electrical/mechanical/pneumatic/hardware troubleshooting, reading blueprints/drawings, and MS Office proficiency

BS or MS in engineering, 10-15 years cGMP experience, 8+ years leadership experience. Experience with complex electromechanical products and knowledge of production standards. Analytical problem-solving skills are essential

Seeking a candidate with at least 3 years of experience in Medical Device Manufacturing and a strong knowledge of CFR Part 820 & ISO 13485. Lean/Six Sigma certification and IQ/OQ/PQ knowledge are preferred. Strong communication and organizational skills are essential

5-10 years of experience in cGMP environment, BS or MS in mechanical engineering, and 4 years of leadership experience

3+ years in manufacturing, 1+ year lead experience. Knowledge of cGMP/GDP standards. Good communication & teamwork skills required

2+ years of manufacturing experience, including assembly and documentation, required. Good communication skills and a willingness to learn are essential