- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …capabilities within a biotech or pharmaceutical setting + Expertise in navigating regulatory frameworks and ensuring compliance within medical affairs function + ... As a senior leader within Medical Affairs, the Executive Director will serve as a strategic thought partner and Chief of Staff to the Vice President of Medical… more
- Guidehouse (Philadelphia, PA)
- …all levels, to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Do you think you are up ... & reimbursement; product commercialization; franchise & business unit strategy; corporate strategy; regulatory & compliance . + 3 plus years leading project… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …SOPs, GPP (Good Publication Practices), ICMJE guidelines, and global regulatory /legal requirements, establishing governance frameworks to ensure compliance ... The Senior Director , Medical Communications, CNS directs and provides strategic...teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory , Commercial) to ensure global and US alignment +… more
- J&J Family of Companies (Spring House, PA)
- …**Johnson & Johnson Innovative Medicine is recruiting for a Medical Director - Clinical Research, Oncology. They will be a member of ... with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the disease area leader… more
- CSL Behring (King Of Prussia, PA)
- …timely, and compliant case management across global PV activities. + Monitor regulatory compliance within case processing workflows, ensuring alignment with ... and implement innovative case management strategies across the Enterprise ensuring compliance with regulatory obligations and scientific excellence. The… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at CMOs ... and transported in a controlled way that is in accordance with regulatory expectations and applicable cGMP/GDP quality standards. This role will direct Biologics… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …SOPs, GPP (Good Publication Practices), ICMJE guidelines, and global regulatory /legal requirements, establishing governance frameworks to ensure compliance ... **Job Summary** The Senior Director , Medical Communications, Nephrology & Immunology directs and...teams (eg, Global Integrated Evidence & Innovation, Clinical Development, Regulatory , Commercial) to ensure global and US alignment +… more
- UPMC (Pittsburgh, PA)
- …to Perfusion Services division. + Assume leadership role as research associate managing project oversight, grant preparation, student and director mentoring of ... UPMC Procirca is looking for a Sr. Director Perfusion Services to lead their dedicated team! This UPMC system-wide position is responsible for the operational… more
- Merck (West Point, PA)
- …**Sr. Principal Scientist - Device Technical and Engineering Lead (Sr. Director Equivalent)** Our company's Device Product & Process Development (DPPD) Team ... ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead… more
- Teva Pharmaceuticals (West Chester, PA)
- …drug development and GxP requirements as knowledge of local, regional and global regulatory compliance (ICH, GMP, EPA, OSHA, DEA, etc.) are integral ... CMC Biologics Quality Control Director , Physiochemical Testing Date: Nov 15, 2025 Location:...stability testing, raw materials testing, contract lab testing, and regulatory submissions. The incumbent may also participate in/provide oversight… more