- Merck (Rahway, NJ)
- … regulatory , company, and customer requirements. **Principal Responsibilities** + Lead /contribute to device development, design controls and risk management ... **Job Description** **Position Description:** ** Device Development Associate Principal Scientist - Development Strategy, Design Controls and Risk Management**… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** The Associate General Counsel, Regulatory Law and Compliance will be a member of the Regulatory Law Group and will report to the ... grow and become your best self. Become a **maker of possible** with us. The Associate General Counsel, Regulatory Law and Compliance will be a member of the… more
- Bristol Myers Squibb (Princeton, 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
- Novo Nordisk (Princeton, NJ)
- …regulatory agencies. Supervise designated personnel. Relationships Report to the Director/ Associate Director/ Lead Regulatory Scientist/Sr. Manager ... related experience; including hands on related pharmaceutical or medical device /pharmaceutical combination product experience and actual regulatory experience… more
- J&J Family of Companies (Trenton, NJ)
- Sr Clinical Research Associate - 2406209639W **Description** At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us ... Medtech companies is recruiting for a Sr Clinical Research Associate , located anywhere in the United States. For more...+ Provide coaching and training to junior employees. + Lead in the investigation of all discrepancies in study… 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
- Integra LifeSciences (Plainsboro, NJ)
- …help improve outcomes. The ** Lead Quality Inspector** serves as a Lead Associate , Quality Inspector for the Plainsboro Manufacturing Site, Collagen ... Manufacturing Center (CMC). The lead associate is responsible for performing and/or...policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory … more
- Merck (Rahway, NJ)
- …on access, pricing/reimbursement, intellectual property, and trade policy + Ability to . lead change management strategies, master complex policy, regulatory and ... **Job Description** **Position Description:** ** Associate Director, Policy Advocacy** The Associate Director, Policy Advocacy serves as the senior expert in the… more
- Takeda Pharmaceuticals (NJ)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director, Programming in Cambridge, MA, where you will oversee and direct ... applicable to the design, analysis of clinical trials and regulatory submissions. + Work with ICH-GCP guidelines for clinical...quality execution of the deliverables by assisting Programming CoE lead . + A SME in the special data types… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …manage business opportunities and risk appropriately. **Essential Responsibilities:** + Lead the SCG Offer Development Contracting capability within the Commercial ... policies, procedures and overall general provisions across customer segments + Lead a defined contract review/approval workflow process, ensuring appropriate process… 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
- 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
- Merck (Rahway, NJ)
- …opportunities in support of our company's business priorities. Reporting to the Associate Vice President, Strategic Planning & External Engagement, this person will ... impact our company and industry and serving as a strategic partner to the Associate Vice President (AVP) on engagement across Global Public Policy (GPP) and the… more