- Danaher Corporation (Timonium, MD)
- …Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. Director Global Quality and Regulatory ... ideas into impact - innovating at the speed of life. As a global leader in high-tech filtration, separation, and purification, Pall Corporation thrives on helping… more
- Merck (Harrisburg, PA)
- **Job Description** The Executive Director (ED) for Field Medical Affairs in the US understands our Company's corporate and products/portfolio strategies and ... work cross-functionally with the Global Medical and Scientific Affairs Therapeutic Area...in a highly matrixed environment is critical. The Executive Director provides strategic and tactical direction to the field… more
- Sumitomo Pharma (Harrisburg, PA)
- …Strateg** **y (** **Hematology/Oncology** **)** will be a key member of the Medical Affairs team reporting to the Executive Director , Medical Affairs ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...launch strategy and guide the tactical implementation of Medical Affairs plans. The Associate Director will also… more
- Takeda Pharmaceuticals (Exton, PA)
- …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... and compliance with regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the organization. Identify … more
- Eurofins (Lancaster, PA)
- …to the entire product lifecycle, from pre-clinical and clinical support to regulatory affairs and market access. Key Responsibilities: + Strategic Leadership ... the entire network of Eurofins companies. Position Overview: The Director of Consulting Services will lead and develop our...test result management. + Life Cycle Management and Outsourced Regulatory Affairs : Offer ongoing support in … more
- Merck (West Point, PA)
- … Global Clinical Supply, Global Clinical Trial Operations, Translational Medicine, Global Regulatory Affairs & Clinical Safety and Quality functions ... **Job Description** The Executive Director of Global Clinical Supplies Quality...of Quality professionals assuring the reliable availability, quality and regulatory compliance of clinical supplies in support of the… more
- J&J Family of Companies (Malvern, PA)
- …strategies, ensuring the successful advancement of our innovative therapies through global regulatory filings. **Responsibilities:** + Lead and manage a ... in their roles. + Collaborate cross-functionally with R&D, quality assurance, regulatory affairs , and manufacturing teams to integrate analytical strategies… more
- Sumitomo Pharma (Harrisburg, PA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... highly motivated, and experienced individual for the position of **Senior Director , Commercial Strategy and Launch Lead, Heme/Onc.** **Job Duties and… more
- Merck (Harrisburg, PA)
- …ethics committees, and internal auditors in conjunction with CCQM, compliance, Regulatory , Pharmacovigilance (PV) and Medical Affairs . + Responsible and ... **Job Description** The Clinical Research Director (CRD) is the Clinical Operations lead in...delivery. + A complete understanding of ICH GCP and Global /Regional/Local regulatory requirements is required. + Strong… more
- Endo International (Malvern, PA)
- …communication platform + Understand and adhere to FDA, DEA and internal regulatory affairs guidelines. + Develop advocacy strategy and resulting tactics ... develop and deliver life-enhancing products through focused execution. Our nearly 3,000 global team members understand the important role we play in delivering… more
- Teva Pharmaceuticals (West Chester, PA)
- …within drug development teams and with other internal partners (eg DMPK, Regulatory Affairs , Clinical Development, and Biostatistics). + Monitor timelines, ... Director Pharmacometrics Date: Mar 16, 2025 Location: West...customers. + Proactively contribute into key pre-clinical, clinical, and regulatory documents including; clinical study protocols, clinical study reports,… more
- Teva Pharmaceuticals (West Chester, PA)
- …their interdependent functions, including R&D, intellectual property, supply chain, finance, and regulatory affairs . This role will also help oversee internal ... and new people to make a difference with. **The opportunity** The Sr. Director , Associate General Counsel, Transactions & Corporate Affairs role reports directly… more