- Englewood Lab, Inc (Totowa, NJ)
- Title: Regulatory Affairs Associate Reports to: Manager of Regulatory Affairs Department: Quality / Regulatory Responsibilities: + Assist the ... of the Head of Quality / Regulatory . + Assist the Manager of Regulatory Affairs during periodic quality reviews, regulatory updates, and annual GMP… more
- ManpowerGroup (Clark, NJ)
- **Senior Regulatory Affairs Associate (Multiple position)** **133 Terminal Ave. Clark, NJ - Onsite role** **6+ month contract with high potential for ... to join their innovative team. Are you a **Senior Regulatory Affairs Associate ** with a...to providing equal employment opportunities in a professional, high quality work environment. It is the policy of ManpowerGroup… more
- ManpowerGroup (Rahway, NJ)
- JOB TITLE / VERSION: Associate Principal Scientist, Regulatory Affairs DIVISION- R&D DEPARTMENT: Global Regulatory Affairs - CMC LOCATION: Rahway, NJ ... Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in… more
- System One (Rahway, NJ)
- Job Title: Associate Principal Scientist, Regulatory Affairs Location: Rahway, NJ (Hybrid) Hours/Schedule: Mon- Fri; 8am- 5pm Type: Contract Responsibilities ... Associate Principal Scientist is responsible for developing CMC regulatory submission strategies and timelines for assigned pharmaceutical projects/products in… more
- Bristol Myers Squibb (Madison, NJ)
- …years in the industry with at least 4+ years of US Medical Device Regulatory Affairs experience **Key Competencies** + Experience in successfully leading teams; ... careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …More Years in the pharmaceutical industry preferred + 1 or More Years in regulatory affairs required + Experience in (s)NDA/BLA filing to FDA preferred ... support across all global projects; meet aggressive deadlines to ensure that regulatory agencies receive timely and quality submissions, shortening the review… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …pharmaceutical industry experience required + 4 or More Years of direct regulatory affairs experience, including US labeling experience required + Experience ... This position serves as the GRA labeling expert to the Global Regulatory Team (GRT) and independently provides strategic and operational leadership on product… more
- Bristol Myers Squibb (Madison, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, US Medical, Multiple Myeloma will report to the Director, US ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will support the… more
- Catalent Pharma Solutions (Somerset, NJ)
- …NJ is hiring a Senior Regulatory and Compliance Specialist for the Regulatory Affairs Group. The Senior Regulatory and Compliance Specialist candidate ... and the greater organization as it touches various functional areas including: Supplier Quality , Regulatory Compliance, DEA, and Quality Management Systems.… more
- RWJBarnabas Health (Somerset, NJ)
- …should be in a closely related field such as health/business administration, regulatory compliance, accreditation or licensure associate , business development or ... Regulatory Planning Manager (Hybrid) - Somerset, NJReq #:0000170498.../ Management Status:Full-Time Shift:Day Facility:RWJBarnabas Health Corporate Services Department:External Affairs and Policy Location: SBC Corporation, Somerset, Somerset, NJ… more
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- … Affairs , Quantitative Clinical Pharmacology, Clinical Safety and Pharmacovigilance, Regulatory /Risk Management, Quality Assurance, Medical Affairs , ... design efficient, adaptable, and scalable architectures in accordance with company policies, regulatory standards, and integration methodology. 15 E - Work with the… more
- Merck (Rahway, NJ)
- …Evidence, Global Discovery, Preclinical and Translational Medicine, Global Medical and Scientific Affairs , and Global Regulatory Affairs and Clinical Safety ... **Job Description** The Associate Principal Scientist, General Medicine Publications Medical Writing, works with scientists in our company's Research Labs and… more
- Sanofi Group (Bridgewater, NJ)
- **Job title** : Associate Director, Global Oncology Corporate Communications **Location:** Cambridge, MA 50% remote working; limited travel expected. **About the ... of patients around the world. Sanofi is looking for a proactive, high-energy Associate Director to join the Global Specialty Care Communications team to support… more
- Sanofi Group (Morristown, NJ)
- **Job Title:** Associate Director, Consumer Marketing - US Rare Hematology **Location** : Cambridge, MA **_About the Job_** This role will drive consumer marketing ... include, HCP marketing, Global Marketing, Sales, Research & Development, Medical Affairs , Business Development, Market Research, Life Cycle Management and Finance… more
- Merck (Rahway, NJ)
- …with a cross-functional Senior/ Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We… more
- Hackensack Meridian Health (Edison, NJ)
- …compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries ... as liaison between principal investigators, sub-investigators, clinical research nurses and regulatory specialists on all regulatory issues and changes within… more
- Sanofi Group (Bridgewater, NJ)
- …clinical care. We curate patient and scientific evidence and partner with commercial, regulatory , R&D, market access, and external affairs teams to develop ... and gastrointestinal diseases. **Main Responsibilities:** The Early Pipeline Gastroenterology Associate Medical Director reports to the Global Medical Head of… more
- Hackensack Meridian Health (Hackensack, NJ)
- …and equipment technician. Ensure departmental compliance with Medical Center and regulatory agency standards. Operate department(s) within approved budgets. Promote ... quality services through the development of Performance Improvement programs....Ensures that all respiratory staff are in keeping with regulatory agency requirements and facility policies and procedures relative… more