- J&J Family of Companies (Raritan, NJ)
- …of America **Job Description:** Johnson & Johnson is currently seeking a Site Based Compliance Manager to join our Regulatory Compliance team located in ... Raritan, NJ. The **Site Based Compliance Manager ** is highly visible to the...experience is required. + Knowledge of cGMP regulations and FDA /EU Guidance related to the manufacture of biologics or… more
- Integra LifeSciences (Princeton, NJ)
- …material remediation experience. + Experience in implementing remediation programs, and working with compliance frameworks such as FDA , ISO 13485, and EU MDR is ... project plan; + Reporting on the sites' progress to the ECMP Project Manager ; + Being responsible for the site(s) ECMP documentation and schedule; + Coordinating… more
- United Therapeutics (Trenton, NJ)
- …their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... about pharmacovigilance! You are a team player who loves quality, compliance , finding solutions and ensuring training standards are implemented and successful.… more
- Ascendis Pharma (Princeton, NJ)
- …to working together as one team to achieve extraordinary results. The Senior Manager Regulatory Affairs, Advertising and Promotion will be an internal expert on US ... FDA regulations, guidance, and enforcement trends governing the promotion...promotion of prescription drug and biologic products. The Senior Manager Regulatory Affairs, Advertising and Promotion is responsible for… more
- United Therapeutics (Trenton, NJ)
- …their daughter's pulmonary arterial hypertension (PAH). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial ... solutions. The purpose of the Senior/Patient Advocacy & Medical Society Engagement Manager is to manage patient advocacy and medical society relationships within… more
- Kedplasma (Cinnaminson, NJ)
- …Operates within the scope of EU Guidance on Good Manufacturing Practice and FDA cGMP 21CFR. **ESSENTIAL JOB FUNCTIONS** Every effort has been made to make ... corrective action(s) as needed. . Responsible, in collaboration with the Center Manager , for overseeing all activities related to product quality, and ensuring… more
- Terumo Medical Corporation (Somerset, NJ)
- …+ Ongoing collaboration with medical, regulatory and legal partners to assure compliance with FDA regulations US laws and appropriate clinical representation ... Brand Communications Manager Date: Aug 1, 2025 Req ID: 4732...commitment to patient safety and product quality by maintaining compliance with all TMC Quality Systems requirements. This includes… more
- Actalent (Princeton, NJ)
- We are seeking a dedicated Senior Clinical Project Manager responsible for overseeing the planning, execution, and management of clinical trials across multiple ... phases. This role ensures compliance with regulatory requirements, timelines, and budget constraints while...clinical trials. + Strong understanding of GCP, ICH guidelines, FDA , EMA, and other regulatory requirements. + Experience managing… more
- Integra LifeSciences (Princeton, NJ)
- …ensuring full compliance with US Customs and Border Protection (CBP), FDA , and other government agency regulations for both imports and exports. This position's ... set new standards of care. The **Import/Export Compliance Specialist** plays a critical role in...department + Dedicated assistance in country-of-origin validation + Assist Manager and Team with trade sanctioned country due diligence… more
- J&J Family of Companies (Raritan, NJ)
- …& Development Quality (RDQ) is recruiting for **Clinical Supplier Quality Manager .** The preferred locations are: **Raritan, NJ, Titusville, NJ, Bridgewater, NJ, ... on their journey to wellness. Learn more at https://www.jnj.com/medtech The Manager , Clinical Supplier Quality is responsible for ensuring robust procedures and… more