- Merck & Co. (Rahway, NJ)
- …Required experience and skills: Min. 5-10 years of experience with Pharmaceutical Regulatory Affairs Operations with Labeling Process and/or Digital Enablement ... Training Programs, FDA Regulations, Management Process, Pharmacovigilance, Policy Implementation, Regulatory Affairs Compliance, Regulatory Compliance, … more
- Merck & Co. (Upper Gwynedd, PA)
- … regulatory issues to GRACS CMC management, as neededDemonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the ... Job DescriptionGRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval...Regulatory Compliance, Microbiology, Molecular Microbiology, Pharmaceutical Process Development, Regulatory Affairs Compliance, Regulatory … more
- Merck & Co. (South San Francisco, CA)
- …as immunology, neurology, cardiometabolic and others as needed by the pipeline.Work with Regulatory Affairs to ensure that regulatory documents (eg, IDEs, ... Job DescriptionThe Associate Vice President (AVP) / Companion Diagnostics will...stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist/ Associate Director, has primary responsibility for ... is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The incumbent… more
- Merck & Co. (North Wales, PA)
- …work collaboratively with other leaders in Clinical Development and Global Regulatory Affairs .--The AVP provides leadership and direction through senior-level ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Canon USA & Affiliates (Lansing, MI)
- ** Regulatory Affairs Specialist - Post Market - req1434** **OVERVIEW** Reporting to the Director Regulatory Affairs , the Regulatory Affairs ... Word, Excel, Oracle, Sales Force, etc. + 2 Years Regulatory Affairs experience in medical device industry...industry required + Minimum Education Level: 2 Year / Associate 's Degree + 4 Year/ Bachelor's Degree (STEM) preferred… more
- Chiesi (Cary, NC)
- …+ Promotional Material/External Communications Responsibilities: + Heads Global Rare Diseases, Regulatory Affairs Ad Promo function for the United States, ... + Prepare Standard Operating Procedures for related activities and provide training to Regulatory Affairs and other departments as appropriate. + Review and… more
- Merck (Upper Gwynedd, PA)
- … issues to GRACS CMC management, as needed + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the company ... **Job Description** GRACS CMC - Associate Principal Scientist, CMC, R4 - Pharm Pre-approval...Regulatory Compliance, Microbiology, Molecular Microbiology, Pharmaceutical Process Development, Regulatory Affairs Compliance, Regulatory … more
- Merck (Rahway, NJ)
- …experience and skills:** + Min. 5-10 years of experience with Pharmaceutical Regulatory Affairs Operations with Labeling Process and/or Digital Enablement ... Training Programs, FDA Regulations, Management Process, Pharmacovigilance, Policy Implementation, Regulatory Affairs Compliance, Regulatory Compliance, … more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- **Job Description Summary** As Associate Director, Regulatory Affairs , you will be responsible for leading RA team members involved in device project ... Advanced degree preferred; medical training preferred. + Minimum 8 years of regulatory affairs experience within the pharmaceutical or medical device industries,… more
- Nestle (Arlington, VA)
- …preferred. Experience: + 5+ years experience in the food industry, primarily in regulatory affairs , regulatory compliance, nutrition or product development. ... groups of trade or scientific associations or other forums to expand Nestle USA representation and impact. + Communicate relevant regulatory trends such as… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …**Key Responsibilities:** + Strategic Medical Leadership: Drive medical affairs activities throughout new product development-from concept ideation through ... commercial launch-ensuring all products meet rigorous safety, efficacy, and regulatory standards. + Clinical Risk Assessment: Collaborate with the Global Medical… more
- BD (Becton, Dickinson and Company) (Sparks, MD)
- …**Job Overview** BD, a leading global medical technology company, is seeking an Associate Director, Medical Affairs - Microbiology Platform to drive innovation ... business decisions. In this strategic role, you will lead Medical Affairs strategy and execution, collaborate cross-functionally, and engage with scientific… more
- BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
- …partner closely with the LSM worldwide business team, regional leadership in the Medical Affairs Function and the Associate Director of Medical Affairs in ... possible** with us. Reporting directly to the business unit Vice President of Medical Affairs , the Director of Medical Affairs has the responsibility to support… more
- Santander US (Boston, MA)
- …to Talk to You!** **The Difference You Make:** The Sr. Associate , Regulatory Relations supports the Regulatory Affairs team by collecting, reviewing, ... Senior Regulatory Relations Associate Country: United States...entities. + Implements standards and procedures to support the Regulatory Affairs function. Maintain documentation and supporting… more
- J&J Family of Companies (Irvine, CA)
- …health for humanity. Learn more at https://www.jnj.com **Job Function:** Medical Affairs Group **Job Sub** **Function:** Medical Science Liaison **Job Category:** ... to wellness. Learn more at https://www.jnj.com/medtech **Posting Title: - Associate Director, Medical Science Liaison, Cardiac Electrophysiology** Johnson and… more
- Chiesi (Cary, NC)
- …generations, ethnicities, abilities, sexual identities and many other enriching diversities. Chiesi USA Chiesi USA is a specialty pharmaceutical company focused ... is Chiesi." Who we are looking for Purpose The Associate Director, Real World Evidence is a scientific role...diverse set of analyses across the portfolio of Chiesi USA medicines by developing advanced, strategic real-world data capabilities… more
- Merck (Boise, ID)
- …immunology, neurology, cardiometabolic and others as needed by the pipeline. + Work with Regulatory Affairs to ensure that regulatory documents (eg, IDEs, ... **Job Description** The Associate Vice President (AVP) / Companion Diagnostics will...stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …(eg, HIPAA, GDPR). **Cross-Functional Collaboration** + Work closely with Commercial, Medical Affairs , Regulatory , and Legal teams to ensure technology solutions ... Associate Director, IT - Value & Access Date:...including Payer Strategy, HEOR, Pricing & Contracting, and Government Affairs . + Translate business needs into technology requirements and… more
- Merck (Rahway, NJ)
- …**Role Summary** + Under the guidance of a senior leader, an Associate Principal Scientist/ Associate Director, has primary responsibility for planning/managing ... is expected to work cross-functionally with clinical development, medical affairs , biostatistics, market access, commercial and country affiliates. The incumbent… more
