- Merck & Co. (North Wales, PA)
- …Medical Device and Combination Product (MDCP) Quality Assurance Operations team, the Associate Director Quality Engineering & Quality Assurance is responsible ... reviewing and approving medical device/combination product documentation to support regulatory filings and audits of data, policies, procedures, and systems… more
- Merck & Co. (North Wales, PA)
- …development, including a communication cascade plan in conjunction with Director of Commercial Operations (DCO)Contracting point(s).Collaborate with brand teams to ... preference for VaccinesPromotion experience including bringing materials through legal, regulatory , and clinical reviewExperience in or working with sales… more
- Merck & Co. (North Wales, PA)
- …cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically, the Director may be ... statistics, and manufacturing to manage clinical development projects; andAssist the Senior Director , Executive Director , and/or Associate Vice President in… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Regulatory Affairs -...will be responsible for acting as and supporting the Global Regulatory Lead (GRL) in strategic vision and ... difference with. **How you'll spend your day** As the Associate Director , Regulatory Affairs you...scientific and regulatory leadership in defining the global regulatory strategy for biosimilar (BioS) projects.… more
- Sanofi Group (Swiftwater, PA)
- **Job title: Device Regulatory Lead ( Associate Director )** + Location: Bridgewater, NJ or Swiftwater, PA or Cambridge, MA **About the job** The Global ... products within the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs, Regulatory CMC and Device Department within Global … more
- J&J Family of Companies (Horsham, PA)
- …- 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate Director Global Labeling Product Leader in Raritan, NJ; ... Associate Director , Global Labeling...experience. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance) including at least… more
- Teva Pharmaceuticals (West Chester, PA)
- …a difference, and new people to make a difference with. **The opportunity** The Sr. Director , Global Regulatory Affairs CMC is responsible to oversee and ... major market health authorities as well as coordinating with global regulatory colleagues in preparing dossiers for...with 4 direct reports (Dir, Sr Manager, Manager & Associate III). The Sr Director , Regulatory… more
- Merck (North Wales, PA)
- …with worldwide regulatory agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or more our company's ... submissions and associated documentation. + Provides expertise as the Global Regulatory Lead to Product Development Teams...but are not limited to:** + Reports to Executive Director or Associate Vice President, Therapeutic Area… more
- Merck (Upper Gwynedd, PA)
- … + Coordinate & facilitate upskilling to embed critical capabilities (to support the PPS director conduit from HHDDA) on behalf of Global Oncology dept. (ie L3, ... + Experience with Learn/Lead/Listen (L3 Next) or other strategic frameworks + Global experience + Knowledge of Company commercial, regulatory , and legal… more
- Publicis Groupe (Philadelphia, PA)
- …www.twitter.com/digitas_health **Job Description** Within Digitas Health, the Vice President, Director , Regulatory Review will provide advice to creative, ... review by Digitas Health's external clients. The Vice President, Director , Regulatory Review supports teams with managing...+ Manage multiple reports (direct or indirect) at the Director , Manager and Senior Associate level including… more
- Merck (West Point, PA)
- …Health, Process Development, Commercialization, Operations, Technical Operations, Analytical, Quality, Regulatory -CMC, and Supply Chain. Associate Director ... **Job Description** **Position Description:** ** Associate Director ,** **Technology Transfer** **(TT)** **Systems...+ Demonstrated creative problem-solving skill. + Strong knowledge of global regulatory guidelines and cGMP principles. +… more
- Teva Pharmaceuticals (West Chester, PA)
- Associate Director , Drug Product Development Date: May 24, 2024 Location: West Chester, United States, Pennsylvania, 19380 Company: Teva Pharmaceuticals Job Id: ... people to make a difference with. **The opportunity** Teva's Global Research & Development (R&D) organization is devoted to...process, and process tech transfer to GMP manufacturing sites. Associate Director is a key leadership role… more
- Merck (West Point, PA)
- … regulatory requirements, regulatory filings and company policies. The Associate Director also ensures that effective and robust Quality systems are ... **Job Description** The Associate Director , ESQL is responsible for...Quality Assurance and Quality Control including solid knowledge of global GMP and regulatory requirements. **OR** +… more
- IQVIA (Wayne, PA)
- Associate Director , Digital Measures, Patient Centered Solutions (PCS) Team **We are innovating the measurement of patient experience through digital health ... Digital Measures, PCS Team** We are seeking a strategy Associate Director to join our team and...on development of digital measures, following rigorous methodologies and regulatory guidance + Contribute to development of strategies, roadmaps,… more
- Merck (West Point, PA)
- …component of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
- J&J Family of Companies (Horsham, PA)
- …skills and the ability to influence is necessary * Experience interacting with global regulatory authorities is also desirable * Approximately 20% travel ... Associate Medical Director , Rheumatology Therapeutic Area...products. She/he will partner with colleagues from Commercial, R&D, Global Medical Affairs, Real-world Value & Evidence, Biostatistics, and… more
- Merck (Upper Gwynedd, PA)
- …and Pharmacometrics -** **Immune/Oncology** team in the role of Associate Director . The team is part of the Global Clinical Development organization ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the Group will work closely with teams of… more
- J&J Family of Companies (Horsham, PA)
- Associate Director , Temperature Strategy & Execution - 2406177829W **Description** Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part ... & Johnson Family of Companies, is recruiting for an Associate Director , Temperature Strategy & Execution within...or Beerse, BE. Within JJIM R&D, CSC holds the global responsibility for delivering all clinical supplies (Devices, API,… more
- CSL Behring (King Of Prussia, PA)
- …used to treat serious and often rare conditions. Could you be our next Associate Director , Clinical Portfolio Execution? The job can be located at any ... **The Opportunity** CSL Behring is a global biotechnology leader, guided by a promise to...Senior Director , Clinical Portfolio Execution As the Associate Director , Clinical Portfolio Execution you will… more
- J&J Family of Companies (Harrisburg, PA)
- Associate Director , Clinical Trial Learning & Training - 2406187889W **Description** Johnson & Johnson is recruiting for an ** Associate Director , ... profoundly impact health for humanity. Learn more at https://www.jnj.com/ . The Associate Director is responsible for deploying organizational training strategy… more
