- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …practices and tools to promote engaged, collaborative, and results-driven work environments. The Director , Global Programs ( Regulatory and Laboratory) ... leadership team, is responsible for developing and implementing a global growth strategy for USP's externally funded regulatory... global growth strategy for USP's externally funded regulatory and laboratory programs . The incumbent will… more
- CBRE (Annapolis, MD)
- Regulatory Change Management Director Job ID 215809 Posted 21-Apr-2025 Service line Corporate Segment Role type Full-time Areas of Interest Legal Location(s) ... United States of America **About The Role:** As a Regulatory Change Management Director at CBRE, you...will be responsible for developing and implementing a comprehensive regulatory change management program to ensure CBRE's… more
- Cardinal Health (Annapolis, MD)
- … experts who provide consulting services in a myriad of capacities, including: + Global Regulatory Strategy Development + Global Regulatory Affairs ... success in obtaining the greatest market share possible. The Director , Business Development with Cardinal Health Regulatory ...Cardinal Health offers a wide variety of benefits and programs to support health and well-being. + Medical, dental… more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- …data management, and medical writing. + Complete understanding of the global regulatory requirements. Demonstrated experience in successful regulatory ... **Job Description** Otsuka is seeking a Director , Global Clinical Development (GCD), who...and other research project team members, and to external regulatory agencies. + Authors program strategies (ie,… more
- Stryker (Annapolis, MD)
- **Key Areas of Responsibility:** + Develops the organization's national, regional, and global regulatory position(s) and strategy based upon assessment and ... competition, opportunities, and to drive regulatory strategy + Integrates regulatory considerations into the organization's global product entry and exit… more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- …for those with CNS disorders, we are seeking a skilled and experienced Medical Director of CNS Early Assets, Global Medical Affairs, responsible for certain ... Franchise Lead CNS Early Assets. **Position Summary:** The Medical Director , Global Medical Affairs, CNS Early Assets... global value and real-world evidence, US and global commercial teams, market access, and regulatory … more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- …post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director , GCD is responsible for all ... and clinical trial implementation and management. + Complete understanding of the global regulatory requirements. + Working knowledge of marketing and… more
- CBRE (Annapolis, MD)
- Business Development Senior Director , Global Occupier Accounts Job ID 210942 Posted 02-May-2025 Service line GWS Segment Role type Full-time Areas of Interest ... is Senior Managing Director , Business Development** The Senior Business Development Director , Global Occupier Accounts, will lead the Healthcare sector Named… more
- Merck (Annapolis, MD)
- …and project delivery. + A complete understanding of ICH GCP and Global /Regional/Local regulatory requirements is required. + Strong Communication skills ... **Job Description** The Executive Director (ED) is the Clinical Operations lead in...for GCTO country operations. Adherence to GCP, local and global policies and procedures to conduct high-quality, inspection ready… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …technical assistance activities across multiple countries in Africa. As the Technical Director for this program , they will provide strategic technical oversight ... access to high-quality medicines through public standards and related programs . USP prioritizes scientific integrity, regulatory excellence, and evidence-based… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …industry and government/ regulatory experience. + Familiarity with global regulatory frameworks affecting pharmaceutical supply chains. **Supervisory ... access to high-quality medicines through public standards and related programs . USP prioritizes scientific integrity, regulatory excellence, and evidence-based… more
- Catalent Pharma Solutions (Harmans, MD)
- …CAPA implementation. + Manage validation lifecycle, ensuring compliance with regulatory expectations and maintaining requalification/periodic review programs for ... **Associate Director , Validation & Engineering** Catalent Pharma Solutions is...Engineering departments in Maryland. Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission… more
- Western Digital (Annapolis, MD)
- …skills. Together, we can build the future of data storage. **Job Description** The Director of the Enterprise Risk Program within Internal Audit is responsible ... insurance; tax-advantaged flexible spending and health savings accounts; employee assistance program ; other voluntary benefit programs such as supplemental life… more
- Gilead Sciences, Inc. (Frederick, MD)
- …Join Kite and help create more tomorrows. **Job Description** We are seeking a Global Director for Quality Systems. This is a critical leadership role ... practices/learnings across the network. + Oversee the development and implementation of global training programs on quality system requirements. + Ensure the… more
- Anywhere Real Estate (Baltimore, MD)
- …Security team, the Director of Risk & Compliance (Data Privacy and Regulatory Compliance) will spearhead the global data privacy and compliance initiatives ... PCI and NYDFS, ensuring robust controls for financial reporting processes. + **Monitor Regulatory Changes** : Stay abreast of evolving global regulations, assess… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- …expertise in chemistry, biologics, engineering, data science, economics, business, and regulatory sciences. The Director for Sustainable Manufacturing brings ... access to high-quality medicines through public standards and related programs . USP prioritizes scientific integrity, regulatory excellence, and evidence-based… more
- Gilead Sciences, Inc. (Frederick, MD)
- …to support the development, implementation, and oversight of facilities and equipment quality programs . + Ensure local and global quality decisions related to ... Join Kite and help create more tomorrows. **Job Description** We are seeking a Director for a Facilities & Equipment Quality Oversight Support role. The role is a… more
- Renaissance (Baltimore, MD)
- …and sensitive information, acts with discretion and is accountable for legal and regulatory compliance. **In this role as Director Compensation & Benefits, you ... When you join Renaissance(R), you join a global leader in pre-K-12 education technology! Renaissance's solutions...best, own our actions, and grow and evolve. The Director of Compensation & Benefits is responsible for the… more
- The US Pharmacopeial Convention (USP) (Rockville, MD)
- … access to high-quality medicines through public standards and related programs . USP prioritizes scientific integrity, regulatory excellence, and evidence-based ... that scientific excellence is driven by a commitment to fairness, integrity, and global collaboration. This belief is embedded in our core value of Passion for… more
- Merck (Annapolis, MD)
- …analyses on programs . + Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics (monoclonal antibodies, ... and verbal communication. + Experience in IND, NDA and other submissions to global regulatory agencies. + An exemplary record of increasing responsibility,… more