- Daiichi Sankyo, Inc. (Bernards, NJ)
- …preferred Experience Qualifications4 or More Years in pharmaceutical, biological and/or medical device operations including first-hand knowledge of drug ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Arthrex (Pendleton, SC)
- Arthrex, Inc. is a global medical device company and a leader in new product development and medical education. We are a privately held company that strives ... protected veteran status, or any other status protected by law.Arthrex, Inc. is a global medical device company and a leader in new product development and … more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …TrackWise) + Extensive knowledge of FDA Quality Systems Regulations 21 CFR Part 820, Medical Device Reporting 21 CFR 803, Report of Corrections and Removals 21 ... **Job Description Summary** The Manager , Complaint Management role is responsible...Regulations for Medical Devices, such as EU Medical Device Regulation (MDR), Canada SOR/98-282 … more
- ICU Medical (Salt Lake City, UT)
- …2 years leadership/supervisory/management experience with demonstrated ability to lead medical device post-market surveillance cross-functional teams. *Physical ... *Position Summary* This positionmanages operations for ICU Medical 's Global Complaint Managementday-to-day activities and workload of direct reports and… more
- DEKA Research & Development (Manchester, NH)
- DEKA R&D has an immediate opening for a Product Complaint Manager to work in a dynamic Medical Device Research and Development environment. The position ... reports to the Program Manager . This is a high visibility role with a...complaint handling in a regulated environment; management and medical device experience preferred. Additional experience and… more
- Boehringer Ingelheim (Ridgefield, CT)
- **Description** The Product Complaint Manager is responsible for being the Subject Matter Expert on the product complaint and adverse events/product ... role provides daily support in Contact Center and Product Complaint meetings as the SME with the primary responsibility...position includes but are not limited to interaction with medical and non- medical contact centers, quality and… more
- Amneal Pharmaceuticals (Bridgewater, NJ)
- Description: Drug Device Combination Product Manager is a position within the Global Quality Management department.This position is a Corporate Quality function ... between departments, CMOs and sites respective to Combination Drug Products and Medical Devices. This position performs the function of Independent Reviewer Role,… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …knowledge and familiarity with BD products + Minimum 3 years of experience with complaint handling, medical device industry, customer relations, complaint ... **Job Description Summary** Under the direction of the Clinical Complaint Manager , the Specialist, will manage activities and procedures associated with… more
- US Tech Solutions (North Chicago, IL)
- …according to procedures. + Assess incoming documentation, including clinical forms and medical information, for complaint data and ascertain compliance to ... determine and document the conclusion(s). + Assist Supervisors and Manager in monitoring complaint and claims workflow to ensure compliance and customer service.… more
- ICU Medical (CA)
- … Medical Product, that I will communicate this information to the appropriate ICU Medical safety or complaint handling group in a timely manner. ICU ... *Position Summary*// The Device Sales Specialist is responsible for meeting and...account via an Account Plan (in conjunction with Area Manager ) * Develop annual territory business plan that outlines… more
- Terumo Medical Corporation (Elkton, MD)
- …a quality, customer complaint investigation/resolution, or clinical experience in medical device industry (disposable devices). + Strongly prefer Clinical ... TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide… more
- J&J Family of Companies (Santa Ana, CA)
- …product complaints, reportability assessment decisions per Health Canada Drug and Medical Device regulations including global regulations. Adheres to ... work experience. * Knowledge and understanding of FDA, EU, EUMDR, Canada Medical Device Regulations and applicable worldwide regulations, standards and… more
- Cirtec Medical (Lowell, MA)
- …of education and experience + Minimum 7 years of experience in a regulated medical device environment, preferably as a Sr or Principal Quality Engineer or ... to the successful candidate.** A day as a Quality Manager at Cirtec Medical You will lead...complaints. + Experience with Class II and Class III medical device development and manufacturing. + Demonstrable… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …from customer calls or correspondence. + Monitor any death or serious injury medical device report (MDR) records through investigation completion to closure ... **Job Description Summary** The Manager , Clinical Specialist Team is responsible for overseeing...to assess if they represent reportable adverse events for medical device reporting. + Incorporate site visit… more
- Terumo Medical Corporation (Somerset, NJ)
- …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $5+ billion in sales, 20,000+ employees worldwide ... Associate Product Manager Date: Aug 29, 2024 Req ID: 3317...two years of relevant work experience, preferably in the medical device industry. Basic computer software skills,… more
- ITW (Elk Grove Village, IL)
- …of custom plastic insert molded filtration and flow control components for global OEM medical device customers. d components to global medical device ... experience, with multi-site experience (with global cultural awareness), preferably in medical device , required. + Strong P&L Leadership, financial acumen.… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Description** Global MDR Analyst II is responsible for supporting medical device adverse event reporting within the complaint handling process. This position ... device guidance documents. This position requires working knowledge of medical device quality systems, FDA regulations relative to complaint handling and … more
- Bausch + Lomb (Clearwater, FL)
- …or Tecnical field. + Supervisory experience, minimum 3 years' experience in a regulated medical device or pharmaceutical industry in a quality discipline. + ... training, compliance (internal auditing, supplier management and CAPA), and complaint investigation. Develop and monitor quality improvement and validation...Medical Devices experience. + Knowledgeable of ISO 13485 and… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …Qualifications** + 4 or More Years in pharmaceutical, biological and/or medical device operations including first-hand knowledge of drug manufacturing, ... pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and… more
- Olympus Corporation of the Americas (Center Valley, PA)
- …Olympus manufacturing and/or service center. **Preferred:** + Proficient understanding of medical device regulations both domestic and international with ... Every day, we live by our philosophy, True to Life, by advancing medical technologies and elevating the standard of patient care so people everywhere can fulfill… more
