- Teva Pharmaceuticals (West Chester, PA)
- Senior Director , Associate General Counsel, Global Regulatory Compliance Date: Oct 17, 2024 Location: West Chester, United States, Pennsylvania, 19380 ... people to make a difference with. **The opportunity** The Sr. Director , Associate General Counsel, Global Regulatory Compliance role reports directly to the… more
- Merck (North Wales, PA)
- **Job Description** We are seeking a Senior Director (Sr. Principal Scientist) Global Regulatory Affairs Liaison with a visionary, growth-oriented ... drive our strategic priorities. **Summary, Focus and Purpose** The Senior Principal Scientist | Regulatory Affairs Liaison...product labeling and obtain shortest time to approval by global regulatory agencies. You will independently manage… more
- Merck (Upper Gwynedd, PA)
- **Job Description** We are seeking a Director (Principal Scientist), Global Regulatory Affairs Liaison with a visionary, growth-oriented mindset that can ... product labeling and obtain shortest time to approval by global regulatory agencies. + Reports to Associate... agencies. + Reports to Associate Vice President, Executive Director , or Senior Director in… more
- Fujifilm (Trenton, NJ)
- **Overview** The Senior Director Global Quality Assurance, Audits & Inspections will be responsible for audit/CAPA activity timeline management, review of ... - what we call Genki. Join us as our Senior Director Global QA, Audits...Global Quality audit program to assure compliance with regulatory requirements across FDB as well as supporting the… more
- Pfizer (Collegeville, PA)
- …and vaccines. **What You Will Achieve** The Senior Manager, Global Regulatory Strategy for Oncology provides support to Director and above regulatory ... professionals by executing against the global regulatory plan for one or more products. This position...development and preparation of regulatory documentation to regulatory authorities. As a Senior Manager, your… more
- Pfizer (Collegeville, PA)
- …into our manufacturing, quality, and cross-functional applications at Pfizer. We are seeking a Senior Director of Global Supply Engineering & Sustainment to ... (DM) Team's mission is to simplify processes and experiences to drive Pfizer Global Supply (PGS) outcomes. DM is responsible for the digital transformation of all… more
- CSL Behring (King Of Prussia, PA)
- The Sr. Director , Head of Global Medical Information will oversee the global core functions of Medical Information across all therapeutic areas/products at ... *Oversee the creation and communication to local affiliates of global scientific response documents ensuring scientifically accurate, evidence based, balanced… more
- CSL Behring (King Of Prussia, PA)
- …across US, International and above-market functions. As the lead of the global market research share service, you will be responsible for overseeing all ... in overall primary market research methodologies and develop a best-in-class global shared services team **Qualifications & Experience Requirements:** + Minimum of… more
- Merck (Trenton, NJ)
- …Description of Position-** This position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). ... Japan, Australia and Brazil + Stay abreast of evolving global regulatory landscapes for medical device and...analysis of data for management review. **Reports to** - Director Regulatory Compliance, Device Quality and … 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 ... standards and policies and business objectives. Actively participate in labeling and global regulatory team meetings to ensure support for anticipated… more
- Lilly (Philadelphia, PA)
- …people around the world. **Position Overview:** The Associate Director - CMC Regulatory is responsible for leading global CMC regulatory activities for ... better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees...tools to effectively communicate the status of ongoing CMC regulatory projects to cross-functional teams and senior … more
- Teva Pharmaceuticals (West Chester, PA)
- …key documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Senior Director will provide input ... the clinical leadership of INDs, NDAs, BLAs, and other global regulatory filings. **How you'll spend your...regulatory filings. **How you'll spend your day** The Senior Director will foster relationships with opinion… more
- Takeda Pharmaceuticals (Exton, PA)
- …FDA law and regulations for development of marketing materials, including representation on global regulatory and labeling teams. + Provide leadership related to ... true to the best of my knowledge. **Job Description** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review out of our Lexington, MA… more
- Chemours (Wilmington, DE)
- …markets, and redefine industries-one improvement at a time. Chemours is seeking a ** Director of Regulatory Advocacy** to join our growing **Government Affairs** ... at our **Washington, DC** office. The successful candidate will join Chemours' Global Government Affairs Group with a primary responsibility for supporting US… more
- Merck (West Point, PA)
- …includes multiple assets moving through near-term late development milestones. The IDVAX Senior Director is responsible for driving the portfolio forward ... biologics and novel modalities, and inform dose selection and go/no-go decisions. As the Senior Director for the IDVAX therapeutic area, you will be responsible… more
- Spark Therapeutics Inc. (Philadelphia, PA)
- …as Clinical Development Lead will provide clinical development support and guidance into global regulatory interactions, will assist the Medical Affairs team, as ... Senior Medical Director - Neurology **Date:**...timelines. + Serves internally as clinical development expert for global regulatory interactions; collaborate with Regulatory… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …+ Appropriately escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned ... life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will...+ Working within Labeling Team and GRA + Represents Global Labeling at Global Regulatory … more
- Takeda Pharmaceuticals (Exton, PA)
- …the best of my knowledge. **Job Description** About the role: Join Takeda as a Senior Manager, US Medical Ad/Promo Regulatory Review where you will serve as an ... the US Medical team, you will report to the Director , Ad/Promo Regulatory Review. You will be...promotional and disease state materials. + May present to senior management, and present regulatory topics to… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …my knowledge. **Job Description** **About the role:** Join Takeda as a Senior Medical Director , Pharmacovigilance in Gastrointestinal and Inflammation (GI2). You ... to the Takeda Safety Board and similar forums. The Senior Medical Director will be a key...submissions, investigational and new drug applications and interactions with regulatory authorities worldwide. + Assists the Global … more
- JPMorgan Chase (Wilmington, DE)
- …risk management shapes our global tech resilience. As a Tech Risk Assurance Director in the Cyber and Tech Controls line of business, you will provide confidence ... the dynamic landscape of evolving cyber threats, technology advancements, and global regulations. The primary responsibilities are to support the cybersecurity… more