- ThermoFisher Scientific (Cranbury, NJ)
- …is safe or helping find cures for cancer. **Discover Impactful Work** As a Sr. Manager , Regulatory Affairs, you will play a crucial role in interpreting and ... and communicate the impact of relevant global regulations, guidelines, and evolving regulatory trends relating to pharmaceutical product development in the area… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- …drug products and drug-device combination products. Ensure compliance with global regulations ( FDA , EMA, ICH, WHO) and anticipate regulatory changes impacting ... strategies for post-approval changes, line extensions, and global harmonization of product registrations. Monitor and implement regulatory updates impacting… more
- Stryker (Mahwah, NJ)
- **Senior Manager , Regulatory Affairs - Joint Replacement Division** **Location:** Hybrid - Mahwah, NJ As the **Senior Manager , Regulatory Affairs** , you ... global regulatory strategies, submission preparation and approvals for new product launches and patient-specific solutions. You will work across the … more
- J&J Family of Companies (Titusville, NJ)
- …Johnson & Johnson Innovative Medicine R&D is recruiting for a Manager , Regulatory Scientist. This position is a hybrid role ... in Titusville, NJ; Raritan, NJ; Spring House, PA; or San Diego, CA. The Manager , Regulatory Scientist is a regulatory specialist with project management… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …a **maker of possible** with us. **Job Overview** Working closely with the Director of Regulatory Affairs, the Regulatory Affairs Manager - RA Strategy Lead ... will provide proactive regulatory surveillance. They will develop regulatory strategies for product creation and market entry. They will also serve as the … more
- Oracle (Trenton, NJ)
- …our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical insight into ... for Clinical Evaluation Reports (CERs), including alignment with EU MDR and FDA regulatory requirements. . Oversee usability engineering (IEC 62366), ensuring… more
- Oracle (Trenton, NJ)
- …our next-generation EHR and AI-enabled medical device platforms. As a Clinical Product Manager (Medical Device Focus), you'll provide clinical insight into ... for Clinical Evaluation Reports (CERs), including alignment with EU MDR and FDA regulatory requirements. . Oversee usability engineering (IEC 62366), ensuring… more
- Otsuka America Pharmaceutical Inc. (Trenton, NJ)
- **Job Summary** The Manager , Global Product Quality - Controlled Substances is responsible for ensuring that all activities related to controlled substances ... (CGMP) regulations, Otsuka Quality Standards and US/global (if applicable) regulatory requirements. **Key Responsibilities** + Product Oversight: Provide… more
- Bristol Myers Squibb (Madison, NJ)
- … FDA regulations and guidances. **Responsibilities include:** + Provides regulatory advice, risk assessment and mitigation strategies to Commercial Teams, Medical ... development of promotional campaigns and materials for an assigned product /therapeutic area in order to help ensure the Company's...compliance of all promotions with approved labeling and /or FDA guidances + Ensure regulatory compliance with… more
- J&J Family of Companies (Titusville, NJ)
- …https://www.jnj.com/innovative-medicine We are searching for the best talent for a **Senior Manager , Product Artwork Technical & Automation to join our Digital ... for this exciting opportunity! The selected candidate will work with existing Product Artwork SMEs /team members to lead all technical and automation initiatives,… more