- TalentBurst, Inc. (Cambridge, MA)
- …be as short as 3 months-up-to 6 months.Job Summary: The US Commercial Regulatory Affairs Promotional Review Committee (PRC) Coordinator is responsible for ... tracking of materials during their life cycle 2) interfacing with brand/Originator and regulatory to assist with system execution of Regulatory submissions, 3)… more
- Sanofi Group (Cambridge, MA)
- **Global Regulatory Affairs Lead (GRL)** **Mission statements** + The Global Regulatory Affairs Lead (GRL) is the fully accountable decision ... pharmaceutical /biotechnology experience, including at least 10 years of relevant Regulatory Affairs experience (regionally and global), in early and late… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Molecules is responsible for Gilead's global portfolio of small molecule products in CMC Regulatory Affairs . This position will lead a global group that ... The leader will also be responsible for ensuring that regulatory strategy is deeply integrated into Pharmaceutical ...report directly to Head of CMC Regulatory Affairs at Gilead. **JOB DESCRIPTION** + Lead … more
- CSL Behring (King Of Prussia, PA)
- …used to treat serious and often rare conditions. Could you be our next CSL Plasma Lead for Global Regulatory Affairs , Plasma? This position is located in our ... contribute to the vision, goals and improvement of Global Regulatory Affairs and includes collaboration with external...to enable a and planning to future our requirements. Lead regulatory strategies and activities globally -… more
- Teva Pharmaceuticals (West Chester, PA)
- …Product Submission Team and dossier timelines. + Accountable to Global Regulatory Lead and Global Regulatory Affairs , with matrixed accountability to ... Director Regulatory Affairs - Submission Management -...adaptations needed as challenges arise. + In collaboration with regulatory lead and project leader, conduct scenario… more
- Sanofi Group (Cambridge, MA)
- …The Associate Director, US Regulatory Affairs (RA) serves as the regulatory lead on relative Review Committees (RCs), for products in the Rare Disease, ... and promotion of prescription drugs and biologics. Essential Functions + Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional… more
- Teva Pharmaceuticals (West Chester, PA)
- Senior Manager, Regulatory Affairs (Remote) Date: May 2, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job ... a difference with. **The opportunity** As the Senior Manager, Regulatory Affairs you will be responsible for...you will be responsible for indirectly supporting the Global Regulatory Lead (GRL) in executing the GRL's… more
- Teva Pharmaceuticals (West Chester, PA)
- …(BioS) projects. You will be accountable to lead and/or support the Global Regulatory Affairs (GRA) Team for assigned projects to ensure alignment of the ... Associate Director, Regulatory Affairs - West Chester, PA...be responsible for acting as and supporting the Global Regulatory Lead (GRL) in strategic vision and… more
- Teva Pharmaceuticals (West Chester, PA)
- …+ 10 years of pharmaceutical industry experience + 6 years of Regulatory Affairs experience. **Preferred:** + Advanced degree ( MS, Ph.D. or PharmD) ... Senior Director, Regulatory Affairs CMC , Innovative Medicine...Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: 53444 **Who we are** Together, we're… more
- Teva Pharmaceuticals (West Chester, PA)
- Director, Regulatory Affairs , Strategy - Innovative Medicine (West Chester, PA or Remote) Date: Apr 29, 2024 Location: West Chester, United States, Pennsylvania, ... make a difference with. **The opportunity** The Director, Global Regulatory Affairs , is a strategic role that...for branded products. + As a global or regional lead within a global regulatory team, develops/coordinates/implements… more
- Teva Pharmaceuticals (West Chester, PA)
- Senior Director, Regulatory Affairs II Date: Apr 20, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... make a difference with. **The opportunity** The Senior Director, Regulatory Affairs II will have a knowledge...meet company goals. Has the ability to inspire and lead teams to fullest potential in a positive approach… more
- Takeda Pharmaceuticals (Boston, MA)
- …to bring life-changing therapies to patients worldwide. Join Takeda as a Director, Regulatory Affairs Vaccines CMC where you will provide program leadership and ... programs in various stages of development. You will represent the vaccine regulatory affairs team on cross-functional Takeda Vaccines teams (commercial, clinical… more
- Takeda Pharmaceuticals (Boston, MA)
- …Join Takeda as a Director, GRA CMC Pharmaceuticals , Oligonucleotides where you will lead the GRA CMC Pharmaceuticals regulatory team in the development ... will report to the Executive Director and Head, CMC Regulatory Affairs , Pharmaceuticals . **How you...a Scientific Discipline, Advanced Degree preferred. + 10+ years pharmaceutical Regulatory CMC experience including experience as… more
- BeiGene (San Mateo, CA)
- …capacity with a broad background. + Preferred candidates will have experience working as a lead in Regulatory Affairs across two or more major geographic ... **General Description** + The Senior Director, Global Regulatory Lead will be responsible for...while leveraging expedited pathways where appropriate. The individual has regulatory affairs departmental and cross-functional influence and… more
- BeiGene (San Mateo, CA)
- …and Regulatory experience.** **Preferred candidates will have experience working as a lead in Regulatory Affairs across two or more major geographic ... are met while leveraging expedited pathways where appropriate.** **The individual has regulatory affairs departmental and cross-functional influence and acts as… more
- BeiGene (Emeryville, CA)
- …and substantial working experience. + Preferred candidates will have experience working as a lead in Regulatory Affairs across two or more major geographic ... **General Description** **_:_** + The Director, Global Regulatory Lead , will be responsible for...while leveraging expedited pathways where appropriate. The individual has regulatory affairs departmental and cross functional influence… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Associate Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus ... role, a typical day might include the following:** + Provide interpretation of regulatory authorities' feedback, policies and guidelines. + Lead the development… more
- Regeneron Pharmaceuticals (Basking Ridge, NJ)
- The Director Regulatory Affairs will provide leadership on global regulatory activities for the assigned products. Responsibility will mainly focus on ... role, a typical day might include the following:** + Provide interpretation of regulatory authorities' feedback, policies and guidelines. + Lead the development… more
- Regeneron Pharmaceuticals (Sleepy Hollow, NY)
- …project management excellence to our Immunology & Inflammation Global Medical Affairs Therapeutic Area Heads & Medical Directors. We work cross functionally ... outcomes. Additionally, you will have oversight to all Global Medical Affairs Interventional & Non Interventional Studies, ensuring a base scientific understanding… more
- Stryker (Portage, MI)
- …Here are 10 reasons to join our Regulatory Affairs /Quality Assurance team: https://www.strykercareersblog.com/post/10-reasons-to-join-strykers- regulatory ... a timely manner. We are currently seeking a **Manager, Regulatory Affairs , State Licensing** to join our...the operations of the virtual wholesale entity. + Review regulatory compliance requirements for changes affecting pharmaceutical ,… more
