- Merck & Co. (Rahway, NJ)
- …device development activities including engineering design, engineering analysis and testing, medical device design controls, risk management , test ... more
- Merck & Co. (Rahway, NJ)
- …requirements and quality standards, serving as a subject matter expert in the medical device and pharmaceutical industries.- Partner with manufacturing sites for ... more
- Merck & Co. (Rahway, NJ)
- …and managing external vendors/research partners.Preferred Experience and Skills:Experience with medical device development with understanding of Design Controls ... more
- Merck & Co. (Rahway, NJ)
- …and managing external vendors/research partners.Preferred Experience and Skills: Experience with medical device development with understanding of Design Controls ... more
- Merck & Co. (Rahway, NJ)
- …guidance & standards: 21 CFR Part 421 CFR 82021 CFR 210/ 211EU Medical Device RegulationUSP USP FDA Guidance for Industry, Container Closure Systems ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Clinical data management and/or related industry work experience in a medical device , pharmaceutical, or biotechnology company, or similar environment (eg, ... more
- Aequor (Atlanta, GA)
- …for managing regulatory documentation related to clinical evaluations, particularly for Medical Device Regulation (MDR) remediation and Post Production Risk ... more
- HireLifeScience (Piscataway, NJ)
- …tool for finding Life Science jobs in the Pharmaceutical, Biotechnology and Medical Device industries. Our parent company, Aequor Technologies, LLC. is ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relevant includes clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... more
- Cytiva (Miami, FL)
- …engineering or project engineering role, preferably in healthcare manufacturing or medical device production.2+ years experience with regulatory standards and ... more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …submission of safety reports including electronic submissions, IND safety reports and Medical Device Reports. Collect, review and edit documents necessary for ... more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …possess strong knowledge manufacturing within a regulated industry such as medical device , automotive, or defense.Must be detail-oriented with exceptional ... more
- Lundbeck (Clackamas, OR)
- …from an accredited college or university 2+ years pharmaceutical, biopharmaceutical, biologics, medical device sales or related healthcare sales experience Must ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …relevant includes clinical or basic research in a pharmaceutical company, a medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and ... more
- Cytiva (Pensacola, FL)
- …Assurance, Quality Engineering, or Manufacturing Operations within Life Sciences, Biotechnology, Medical Device , Biopharma, or other FDA or EPA-regulated ... more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …equipment, and quality and regulatory requirements important to pharmaceutical and medical device manufacturing labs.Able to write detailed investigation summary ... more
- Beckman Coulter Life Sciences (Indianapolis, IN)
- …Engineering, or Computer Science preferred)5+ years of prior experience in the Medical Device /Diagnostic/Life Science industry in one of the following: Systems ... more
- Cytiva (Miami, FL)
- …lifecycle management systems, in biotech, pharma, drug product, or medical device document control experience preferredStrong foundational knowledge in ... more
- Cytiva (Miami, FL)
- …Quality, Engineering, Regulatory, or R&D in a regulated industry (ISO 9001, medical device , or pharmaceutical preferred).Experience with root cause analysis, ... more
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