- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …Global Project Team, Safety Management Team, Clinical Safety and Pharmacovigilance Medical Affairs, Companion Diagnostics/ Device Laboratories Vendors/ CROs ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Catalent (St. Petersburg, FL)
- …years auditing experience Experience working in an auditing role within the Pharmaceutical/ Medical Device industry, required Knowledge and understanding of the ... 4 GMPs, 21 CFR Parts 111/210/211 (FDA), ISO, and related International Regulations affecting pharmaceutical products and medical devices… more
- Catalent (St. Petersburg, FL)
- …experience , required Experience working in an auditing role within the Pharmaceutical/ Medical Device industry Knowledge and understanding of the following ... Volume 4 GMPs, 21 CFR Parts 111/210/211 (FDA), ISO, and related International Regulations affecting pharmaceutical products and medical devices Working knowledge… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …relevant includes clinical or basic research in a pharmaceutical company, a medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …relevant includes clinical or basic research in a pharmaceutical company, a medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …relevant includes clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …relevant includes clinical or basic research in a Pharmaceutical company, a Medical device /Diagnostic company, Academic Research Organization (ARO) or Contract ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …drug development and/or post marketing in Clinical research, Pharmaceutical company, CRO or Medical Device setting preferred- 4 or More Years Experience in ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Stryker (Chicago, IL)
- …Degree (Masters in Regulatory Affairs) preferred. + Thorough understanding of FDA and international medical device regulations. + General understanding of ... preferably with medical devices and formulations. + 2-3 years of Medical Device Regulatory Affairs experience required. + RAC certification or Advanced… more
- Abbott (Alameda, CA)
- …or related area. + Advanced level degree + Experience with EU and other international medical device / drugs / pharma regulations and submissions. ... spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues… more
- Olympus Corporation of the Americas (Brooklyn Park, MN)
- … Medical Device Regulations, ISO 13485, ISO 14971, and any other medical device industry international standards. + Experience with risk analysis and ... preferred, Bioengineering, Mechanical Engineering, etc. with relevant educational experience for medical device industry also preferred. Evidence of continued… more
- Abbott (Alameda, CA)
- …scientists. **The Opportunity** Responsible for timely review, documentation and filing of Medical Device Reports, including international vigilance reports ... also have access to: + Career development with an international company where you can grow the career you...division's products. Accountable for meeting the compliance requirements for Medical Device Reporting regulations including (803). This… more
- Motion Recruitment Partners (Lake Forest, CA)
- … Devices Lake Forest, California **Open to Remote** Contract $75/hr - $100/hr An international medical device company is looking to hire Product Security ... working with medical devices or med-tech and have worked with HIPPA/ medical device regulations or FDA approval processes. As well as a strong background in… more
- Abbott (Lake Forest, IL)
- …at multiple levels in the organization. + Manufacturing engineering experience, medical device experience required, international manufacturing experience ... management skills. Six Sigma certification preferred + Manufacturing engineering experience, medical device experience required, international manufacturing… more
- LSI Solutions (Victor, NY)
- …lines, helping to gather regulatory intelligence regarding updates to US and international medical device regulations, and supporting Rest-of-World (ROW) ... to our medical devices, while maintaining compliance with applicable US and international medical device regulations, standards, and guidelines for … more
- IQVIA (Durham, NC)
- …consulting expertise covering EU & US regulations. + GCP consulting knowledge (Pharma & Medical Device ). + Proven international track record in selling ... GMP/QMS services. + Good experience with presenting at GMP/QMS conferences. + Medical Device GMP experience, useful but not essential. + OCM experience. IQVIA is… more
- Abbott (Plymouth, MN)
- …+ Maintains ongoing surveillance and analysis of all pertinent domestic and international medical device regulations to ensure submission requirements ... US device regulations and/or experience with EU and other international medical device regulations and submissions. + Experience with risk management,… more
- Motion Recruitment Partners (Lake Forest, CA)
- …/ Medical Devices Lake Forest, California **Onsite** Contract $70/hr - $100/hr An international medical device company is looking to bring on a Product ... working with medical devices or med-tech and have worked with HIPPA/ medical device regulations or FDA approval processes. You will play a critical role in… more
- Abbott (Chicago, IL)
- …to prepare and compiles technical documents and labeling to support complex US and international medical device regulatory submissions ( _i.e_ ., ... into a single comprehensive package for new and revised US and international medical device regulatory submissions. Challenges conclusions when necessary. +… more
- Motion Recruitment Partners (Lake Forest, CA)
- … Devices Lake Forest, California **Open to Remote** Contract $60/hr - $80/hr An international medical device company is looking to hire a Penetration ... devices, medtech, or related field + Experience with HIPPA, FDA, or medical device regulations + Strong communication skills and ability to work independently… more
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