- CHRISTUS Health (Lake Charles, LA)
- …high-quality, cost-effective care to patients. Responsible in assisting the Director for analyzing, planning, implementing, evaluating, and communicating processes ... behaviors; increases productivity. Clinical Performance Improvement Shares experiences with process performance improvements across multiple areas. Recognizes recurring and… more
- AmerisourceBergen Drug Corporation (Conshohocken, PA)
- …400+ pharmaceutical manufacturing partners, enterprise IT, category management, regulatory assurance, and other various cross-functional teamsEstablish and manage ... senior Data Analysts, Data Analysts, contractors, and data coordinatorsManage the process and contractor resources responsible for the TITHTS manual entry exception… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …role** The Manager of Regulatory Affairs reports directly to the Associate Director of Regulatory Affairs Process Quality. This position is responsible ... **Job Description Summary** Manager of Regulatory Affairs that oversees MMS Infusion products and...Software and Accessories on a global basis from a Regulatory Affairs standpoint. Support will consist of new product… more
- HCA Healthcare (Nashville, TN)
- …Do you want to join an organization that invests in you as a Senior Director Regulatory and Accreditation? At HCA Healthcare, you come first. HCA Healthcare has ... a difference. We are looking for a dedicated Senior Director Regulatory and Accreditation like you to... issues to senior department leadership *Identifying CSRE work process improvements to resolve operational problems and collaborating with… more
- Merck (Rahway, NJ)
- …**Education:** + Bachelor's degree with 12+ years of industry experience, including regulatory and/or compliance area and experience with process management in ... **Job Description** The GRACS Global Process Lead (GPL) is responsible for overseeing and...Lead (GPL) is responsible for overseeing and managing Global Regulatory Affairs & Clinical Safety (GRACS) global business processes.… more
- Regeneron Pharmaceuticals (Troy, NY)
- The Director of CMC Industry and Regulatory Intelligence is responsible for enabling chemistry manufacturing and controls (CMC) quality and compliance excellence ... standards for all CMC operations across Regeneron. As a Director of CMC Industry and Regulatory Intelligence,...+ Good understanding of the drug development and commercialization process , with a focus on CMC + Experienced in… more
- Merck (Rahway, NJ)
- **Job Description** **Principal Scientist / Director , GLOBAL REGULATORY CMC Biologics (R5)** Under general supervision of an Executive Director /Senior ... for developing and implementing Chemistry, Manufacturing, and Controls (CMC) regulatory strategies for our organization's biologics product franchises in accordance… more
- Corewell Health (Grand Rapids, MI)
- Job Summary - Director , Medical Regulatory and Accreditation Collaborates with the VP and senior leadership of Priority Health's Medical Management and ... and processes related to the medical policy life cycle. Essential Functions - Director , Medical Regulatory and Accreditation + Responsible for the development,… more
- Actalent (Boston, MA)
- Position: Director /Sr. Director of Regulatory ...as the modification or adjustment of the job application process or interviewing process due to a ... regulatory professional to join our collaborative team as the Director /Sr. Director of Regulatory CMC. This pivotal role involves providing leadership… more
- J&J Family of Companies (Columbus, OH)
- Director , Regulatory Medical Writing (1 of 4) - 2406211847W **Description** Johnson & Johnson is currently seeking a Director , Regulatory Medical ... potential. At Johnson & Johnson, we all belong. The Director , Regulatory Medical Writing (RegMW) is a...Common Technical Document (eCTD) is required. + Experience conducting Regulatory Medical Writing business process , scenario, and… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Director , Therapy Area Head, Global Regulatory Medical Writing Date: Sep 20, 2024 Location: Parsippany, United States, New Jersey, 07005 Company: Teva ... is a remote opportunity and candidate can sit anywhere in the United States** A Director , in Global Regulatory Medical Writing, reports into Head of Global … more
- Stanford Health Care (Palo Alto, CA)
- …America) **This is a Stanford Health Care job.** **A Brief Overview** The Senior Director of Quality Management and Regulatory Affairs is responsible for the ... strategic planning, oversight and direction of accreditation, regulatory , and licensing across Stanford Health Care. This includes but not limited to continuous… more
- Takeda Pharmaceuticals (Columbus, OH)
- …the best of my knowledge. **Job Description** **About the role:** **Associate Director , Nonclinical Regulatory Writing and Submission Support,** **_Oncology and ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...engage in meaningful work? Join us as an _Associate Director - Nonclinical Regulatory Writer_ _and Submission… more
- Merck (North Wales, PA)
- **Job Description** Reports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible ... and approval of all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional… more
- Bayer (Whippany, NJ)
- …diverse minds to make a real difference, there's only one choice.** **Assistant Director Regulatory Affairs North America Operations** The Assistant Director ... AND RESPONSIBILITIES** The primary responsibilities of this role, Assistant Director Regulatory Affairs North America Operations, are...+ Represent and support the Head of North America Regulatory Affairs to manage issues, process flows,… more
- Takeda Pharmaceuticals (Boston, MA)
- …order to bring life-changing therapies to patients worldwide. Join Takeda as a Senior Director , Global Regulatory Lead, GI & Inflammation where you will define, ... components of regulatory submissions. + Expert knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, Canada, ROW and… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. As an Associate Director , Global Regulatory Affairs Marketed Products you will define, develop ... as applicable. **How you will contribute:** + The Associate Director will be responsible for increasingly complex or multiple... submissions. + Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …35 countries worldwide, with headquarters in Foster City, California._ **Senior Director - Analytical Regulatory ** **Science** **KEY** **RESPONSIBILITIES** The ... Sr Director , Analytical Regulatory Science, is responsible for supervising a team of...have cross-functional leadership roles and may participate in business process development initiatives or represent the company in industry… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Operations Pleasanton, CA, USA * Princeton, NJ, USA Req #386 Tuesday, August 20, 2024 Looking for a chance to make a ... expanding mid-size oncology company in the role of Associate Director , Regulatory Affairs Operations where you will... Operations team by providing guidance, as well as regulatory system and process support for the… more
- Charles River Laboratories (CA)
- …that you can feel passionate about. **Job Summary** We are seeking anexperienced ** Director of Regulatory Services & Compliance** to join our **Insourcing ... San Diego, CA, or San Francisco, CA.** As the ** Director of Regulatory Services & Compliance** ,...forms or to otherwise participate in the resume submission process , please contact a member of our Human Resources… more
