| Job alert | Jobs 1 - 10 of 62 |
Product Development Engineer
Ehub Global Inc
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Providence, RI, 02912
... Laboratory, cleanrooms, biosafety cabinets, etc.) Working in a GxP environment Working under FDA 21CFR part 820 regulations Key Duties and Responsibilities: Effectively collaborates with a fully integrated team to facilitate the success of projects ... - Apr 28
Research Scientist
Germer International - Pharmaceutical Recruiting
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Rhode Island
... LC/MS and/or GC/MS preferred Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance Education: PhD with 2 plus years of experience in pharmaceutical analysis, MS with minimum of 5 years of experience/BS with 8 years of experience. - Apr 28
Quality Assurance Manager
The Goodkind Group, LLC
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East Greenwich, RI, 02818
... or a minimum of 8 years of experience in Quality Assurance in food manufacturing HACCP certification or formal training in Hazard Analysis Critical Control Point FDA Risk-Based Preventive Controls or PCQI formalized training Lean Six Sigma Green ... - Apr 26
CSV Validation Engineer - Strictly W2
Hire IT People, Inc
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Rhode Island
... Minimum of 5+ years of experience working within a medical device environment or other FDA regulated environments. Experience with device-biologic combination products is highly desirable. Experience in the areas of Design Documentation (URS, FRS, ... - May 02
Maintenance Manager
The Dunwoody Group
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Rhode Island
... adjustments Qualifications 5+ years' experience as a maintenance/ mechanics manager Leadership experience in a manufacturing environment Experience with machine making FDA regulated product preferred Bachelor's degree or equivalent work experience - Apr 18
Phlebotomist
eTeam
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Warwick, RI, 02888
... Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research; Recruit and screen patients for clinical trials and maintain subject screening logs; Orient research ... - May 02
Clinical Research Coordinator
eTeam
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Warwick, RI, 02888
... Collect and submit regulatory/ethics documentation as required by the FDA and other regulatory bodies governing the conduct of clinical research; Recruit and screen patients for clinical trials and maintain subject screening logs; Orient research ... - May 02
Senior Analytical Scientist
Pharmaron
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Coventry, RI, 02816
... Experience with NMR, ICP-MS, XRPD, DSC-TGA, LC/MS and/or GC/MS preferred Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance Excellent communication skills, both verbal and written Benefits: Pharmaron cares about our work ... - Apr 03
Senior Analytical Scientist
Pharmaron
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Coventry, RI, 02816
... Experience with NMR, ICP-MS, XRPD, DSC-TGA, LC/MS and/or GC/MS preferred Working knowledge of cGLP/cGMP and applicable FDA, EMA and ICH guidance Excellent communication skills, both verbal and written Benefits: Pharmaron cares about our work ... - Apr 03
Client Services Lead
Rhode Island Blood Center
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Providence, RI, 02908
... Knowledge of AABB, FDA, OSHA, and regulations. Working knowledge of Microsoft Suites. Working knowledge of LIS and BECs. Working Knowledge of Good Manufacturing Practices (cGMP). Skill Attention to detail and organizational skills. Detail oriented. ... - Apr 17