- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …+ Ensure program success by working cross functionally with R&D-Engineering, Marketing, Medical Affairs , Manufacturing, Quality and Regulatory Affairs ... knowledge of material science and engineering principles + Working experience in medical device industry + Familiar with design control process and medical … more
- Wolters Kluwer (Trenton, NJ)
- …Manager** will be calling primarily on Librarians, Information Scientists, Heads of Global Regulatory Affairs , Directors of Medical Affairs , and ... software tools to for-profit corporations including CROs, pharma and medical device companies. The **Senior Account &...+ Proven track record selling into the pharmaceutical and medical device companies, and CRO's (preferred) +… more
- Integra LifeSciences (Plainsboro, NJ)
- …timely technical investigations and provide practical manufacturing solutions, under appropriate regulatory guidelines for Medical Device Manufacture. As ... from Engineering, Manufacturing, Product Development, Marketing, QA, and Clinical & Regulatory Affairs . + Project Management aimed to evaluate, analyze,… more
- Bristol Myers Squibb (Princeton, NJ)
- …Access objectives + Work as part of cross-functional teams-including clinical development, medical affairs , regulatory , and biostatistics-to ensure HEOR ... including data model specifications, project plans, user acceptance testing scripts, device screenshots, site user guides and training slides, and data migration… more
- Robert Half Technology (Mahwah, NJ)
- Description We are looking for a dedicated Regulatory Affairs Quality Assurance Specialist to join our team in Mahwah, New Jersey. In this role, you will play a ... the efficiency and effectiveness of documentation systems. * Support compliance with medical device regulations and quality assurance standards. * Collaborate… more
- Stryker (Mahwah, NJ)
- …the Technical Publications Specialist, you will play a key role in ensuring our medical device labeling is clear, compliant, and accessible, supporting safe and ... records **What you need** **Required Qualifications** + Bachelor's degree in Regulatory Affairs , Engineering, Graphic Design, Technical Writing, or related… more
- Cardinal Health (Trenton, NJ)
- …will also help to support inorganic product opportunities and better define our medical device connectivity strategy. **_Responsibilities_** + Support and be a ... evolution + Collaborate with partners across enterprise, including R&D, Regulatory , Clinical Affairs , Sourcing, Manufacturing, Strategy Functions,...+ 4+ years experience in related field, preferred. + Medical device or global medical … more
- Integra LifeSciences (Princeton, NJ)
- …and Operations to ensure alignment across product lifecycle phases and compliance with medical device regulations (eg, FDA, ISO 13485, MDR). Ensure supplier ... to quality, product development, process technology, operations, supply chain, procurement, regulatory affairs , finance, and human resources. + Prepare and… more
- J&J Family of Companies (Raritan, NJ)
- …Bachelor (Rising Juniors or above), Masters, and PhD who desire a career in the medical device or pharmaceutical industry and are eager to learn technical and ... or PhD in life science, analytical science, data science, regulatory compliance or regulatory affairs ,...to participate in Company employee benefit programs such as medical insurance, sick time, holiday pay, and the Company's… more
- Integra LifeSciences (Princeton, NJ)
- …intercompany loans ; + Providing product counseling and guidance on commercial and regulatory affairs initiatives to ensure compliance with applicable laws and ... with substantial experience supporting international business activities. Pharmaceutical or medical device industry experience preferred; + Comfort navigating… more