- Bristol Myers Squibb (Princeton, NJ)
- …program. Including specialized training for Cyclotron operators and radiochemists, x-ray device users, preclinical imaging, radiochemistry suite, medical staff, ... NJDEP. + Serve as the Cyclotron Particle Accelerator Safety Officer (PASO). Regulatory qualifications/requirements to be eligible as a PASO are noted in… more
- Medtronic (Newark, NJ)
- …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical devices. ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...for all ablation procedures at study sites for investigational device studies to guide the physician on the requirements… more
- System One (Jersey City, NJ)
- …revenue growth. + Strong understanding of the sales process, product knowledge and the medical device market. + Ability to lead, motivate and inspire a team ... + Proven track record in sales preferably in the medical device /manufacturing and/or pharma industry. (ideally selling...field + Strong knowledge of the healthcare industry and regulatory requirements + Book of Business / Network of… more
- J&J Family of Companies (Raritan, NJ)
- …and process controls for manufacturing processes. + Provide technical support for marketed medical device products to other business functions such as ... (Design Of Experiments) and regression analysis. + Prior experience working in the Medical Device industry. + Knowledge of medical device regulations.… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …field required; _Master's degree preferred_ + Expert-level proficiency in ISO 13485, Medical Device Regulation (MDR), and FDA requirements with demonstrated ... ISO frameworks, GMP/GDP protocols, and USP-EP guidelines as they apply to medical device environments + Demonstrated capability to align technical decisions… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. * QA experience in the medical device… more
- Integra LifeSciences (Plainsboro, NJ)
- …a quantitative standpoint. The candidate must be familiar with process flow of a medical device organization, including the regulatory impact of change and ... in a Validation or Quality Assurance role for a medical device or pharmaceutical environment. + Demonstrates excellent organizational and communication… more
- Integra LifeSciences (Plainsboro, NJ)
- …corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to ... incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical device… more
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