Part-Time Manufacturing jobs in New Brunswick, NJ
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PCS/ IMPROVEMENT ENGINEER
Bachelor of Science in Chemical/Mechanical Engineering. At least 5 years of experience in Manufacturing is required. Hands-on experience with SPC tools and advanced data analytical methods. Demonstrated experience in managing and...
| Company | Dupont |
|---|---|
| Address | Parlin, NJ |
| Category | Manufacturing |
| Date Posted | 3 weeks ago See detail |
PCS/ Improvement Engineer
Dupont
Parlin, NJ
Bachelor of Science in Chemical/Mechanical Engineering. At least 5 years of experience in Manufacturing is required. Hands-on experience with SPC tools and advanced data analytical methods. Demonstrated experience in managing and...
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Sr. Quality Assurance Engineer
Enterix
Edison, NJ
Develop and maintain quality systems to ensure compliance with applicable regulations and standards, including FDA, ISO, and CE.? Management, investigation, and reporting of CAPAs and NCR (including root cause analysis) and Effect...
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Quality Systems & Compliance Specialist
Hikma Pharmaceuticals Plc
Dayton, NJ
Assist with ensuring compliance with the FDA CFR, including cGMP and DEA regulations, as well as State Board of Pharmacy rules and regulations. Keep abreast of relevant guidance documents pertaining to 503B production. Monitor and...
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Quality Assurance Specialist
U.s. Department Of The Treasury
Springfield, NJ
Must be a U.S. Citizen or National and provide proof of U.S. Citizenship. (Birth certificate showing birth in the U.S; Unexpired U.S. Passport; Certificate of Citizenship or Naturalization; or Report of Birth Abroad of a U.S. Citi...
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Quality Assurance GMP Intern
Biospace
Basking Ridge, NJ
Defining, measuring, analyzing, and improving identified processes within the quality organization. Performing data analysis for established metrics and identifying potential new metrics. Supporting continuous improvement projects...
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ECQ Engineer
Bristolmyers Squibb
Summit, NJ
Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices. Advanced knowledge of pharmaceutical, manufacturing and laboratory systems and equ...
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