- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- …with FDA and other regulatory authorities. + Experience with device regulatory requirements and development processes for combination productions including ... activities. **In this role, a typical day might include the following:** + Lead CMC/CP product development activities from a regulatory standpoint during early… more
- Bristol Myers Squibb (Madison, NJ)
- …5 years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading ... assessing regulatory risk, and developing global filing strategies. + Co- lead marketing application submission teams for indications that are at regulatory… more
- Bristol Myers Squibb (Madison, NJ)
- …medical device , and/or translational development processes, with ability to lead supportive project management processes + Strong understanding of global ... the patients and health care providers we serve. The Associate Director, Technical Management, reports to the Technical Management...regulatory requirements for companion diagnostic device development… more
- AbbVie (Branchburg, NJ)
- …Team (IEST) lead , Clinical Program Lead and Clinical Science Lead and Clinical Scientist. The Associate Director, Clinical Development should expect to ... on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Associate Director, Clinical Development will have global or regional responsibilities and… more
- L'Oreal USA (Clark, NJ)
- …/ Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 187395 Associate Principal Scientist, Cosmetics Product Safety & ... Clark, NJ Research & Innovation Full - Time 22-Aug-2024 Position Title: Associate Principal Scientist, Cosmetics Product Safety & Toxicology, L'Oreal Research &… more
- Merck (Rahway, NJ)
- …to commercialization. Our development teams ensure robust composition, primary packaging/ device , and process selection through deep fundamental understanding and ... products. Our team is looking for a candidate for the position of Associate Principal Scientist (R4) supporting the Biologics formulation team within Sterile and… more
- Johnson Controls (Totowa, NJ)
- …to all safety standards. How you will do it + Interprets applicable regulatory requirements and ensures that project deliverables meet these as well as specific ... whenever possible. + May manage and complete the loading, device verification, and commissioning of all system controllers as...+ Effectively communicates the status of projects to Project Lead and management as required and assists in preparing… more
- Medtronic (New York, NY)
- …and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, ... one of the fastest growing businesses in the medical device industry and expanding rapidly to serve patients globally....specialist/clinical engineer or relevant hospital experience_ ) or + Associate degree with a minimum of 9 years of… more
- Guidehouse (New York, NY)
- …practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle today's ... all levels, to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Do you think you are up for the… more
- AbbVie (Jersey City, NJ)
- …safety surveillance + Responsible for safety surveillance for pharmaceutical / biological / drug - device combined products + Lead and set the strategy for key ... Instagram, YouTube and LinkedIn. Job Description Purpose: Manages other Associate Medical Directors, Medical Directors, Senior Medical Directors. Leading Product… more
- Medtronic (New York, NY)
- …and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, ... in work schedule and/or workload. + Adheres to financial, regulatory , quality compliance standards and requirements **Qualifications - External**...YOUR RESUME_ + High School Degree and 9+ OR Associate degree and 5+ OR Bachelor's degree and 3+… more
- Guidehouse (New York, NY)
- …practice is an engine of innovation, helping pharmaceutical, biotech, medical device , and diagnostic companies develop custom solutions that tackle today's ... all levels, to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Do you think you are up for the… more