- University of Pennsylvania (Philadelphia, PA)
- …to enhance understand of and compliance with applicable regulations. + The Associate Director for Regulatory Affairs will also serve as the key departmental ... trial compliance and quality assurance through communication of audit results and compliance guidelines. + The Associate Director for Regulatory Affairs… more
- Astrix Technology (Indianapolis, IN)
- ** Associate Director , Quality & Compliance ** Quality Assurance Indianapolis, IN, US + Added - 15/12/2025 Apply for Job Associate Director , Quality & ... + Own batch record review and release, ensuring speed, accuracy, and compliance + Drive investigations, deviations, CAPAs, change control, and SOP execution +… more
- Takeda Pharmaceuticals (Boston, MA)
- …best of my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for ensuring the ... meet quality requirements, auditing and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards,… more
- Takeda Pharmaceuticals (Boston, MA)
- …true to the best of my knowledge. **Job Description** **ABOUT THE ROLE** The Associate Director , GCP Audit & Compliance provides strategic quality oversight ... global network. You will lead the risk-based supplier audit program, drive compliance insights, and partner closely with stakeholders to ensure adherence to GCP,… more
- Boehringer Ingelheim (St. Joseph, MO)
- …through activities such as governance review, project team meetings, planning activities and FDA communications. Associate Director Act as Regulatory Affairs ... of regulatory tools as defined. + Supports specific infrastructural projects as assigned. Associate Director + Responsibility for the safety and efficacy part of… more
- Boehringer Ingelheim (Ridgefield, CT)
- …and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Associate Director , DRA Product Labeling will lead and manage the ... ECTD compliant. + Responsible for the labeling section of NDA Annual Reports. **Requirements** Associate Director : + Bachelor's degree with a focus in Biology or… more
- Bristol Myers Squibb (Madison, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director Commercial Regulatory Affairs** **Description** : The role ... of Associate Director of US Commercial Regulatory Affairs... of all promotions with approved labeling and /or FDA guidances + Ensure regulatory compliance with… more
- United Therapeutics (Research Triangle Park, NC)
- …individual expertise and mentoring or developing a member of your team. The Associate Director , QA Engineering will provide advanced support and subject matter ... pulmonary arterial hypertension ( **PAH** ). Today, we have six FDA -approved therapies that treat PAH, pulmonary hypertension associated with interstitial lung… more
- Takeda Pharmaceuticals (Boston, MA)
- …medicines and make a lasting impact on patients worldwide. Join Takeda as Associate Director , Global Regulatory Lead Oncology where you will be part ... of the global regulatory team. As Associate Director , Global Regulatory Lead Oncology, you...lead as a member of a GRT + Primary FDA contact for projects of responsibility. + Accountable for… more
- Ascendis Pharma (Princeton, NJ)
- …the boundaries of company compliance SOP's and US regulations). The Associate Medical Director is expected to develop and deliver impactful presentations ... As a member of the Endocrine Medical Sciences team for the US business, the Associate Medical Director supports the US Medical Director for deliverables and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA A&P) ... to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you… more
- Takeda Pharmaceuticals (Boston, MA)
- …regulatory strategies in collaboration with their regional counterparts. **Accountabilities:** + The Associate Director will be responsible for complex or highly ... to achieve timely and efficient development and maintenance of programs, while ensuring compliance with applicable regulatory requirements. + Is a leader both in the… more
- Cambrex High Point (Charles City, IA)
- …and inspections. Responsibilities + Responsible for monitoring and maintaining compliance with DEA regulations pertaining to shipping, manufacturing, analytical and ... related to CS handling and mfg. All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to… more
- J&J Family of Companies (Horsham, PA)
- …of America **Job Description:** We are searching for the best talent for Associate Medical Director , US Medical Affairs -Gastroenterology based in Horsham, PA. ... at https://www.jnj.com/innovative-medicine **Purpose:** J&J Innovative Medicine is seeking an Associate Medical Director , US Medical Affairs -Gastroenterology to… more
- Mallinckrodt Pharmaceuticals (Horsham, PA)
- Job Title Associate Director , Manufacturing Operations Requisition JR000015470 Associate Director , Manufacturing Operations (Open) Location Horsham, PA ... Additional Locations Job Description Summary Job Description The Associate Director , Manufacturing Operations will provide leadership and management of… more
- Bristol Myers Squibb (Devens, MA)
- …lives. Read more: careers.bms.com/working-with-us . **Position Summary** Reporting to the Director , Inspection Readiness, the Associate Director will ... Inspection Readiness and will, on a tactical level, execute compliance and inspection support programs in a matrixed organization....with teams and leaders across the BMS network. The Associate Director will support BMS' GMP/GDP Inspection… more
- Catalent Pharma Solutions (Philadelphia, PA)
- ** Associate Director , Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) ... is a full-time salaried position, onsite out of Philadelphia, PA.** The ** Associate Director , Quality Assurance** is responsible for providing leadership and… more
- Catalent Pharma Solutions (Manassas, VA)
- ** Associate Director , Engineering & Maintenance** **Position Summary** + **Work Schedule:** Regular business hours + 100% based on-site Our Manassas, Virginia ... help create engaging new products consumers will love. The ** Associate Director , Engineering & Maintenance** is responsible...reports directly to the site General Manager / Site Director . **The Role** + Ensuring full compliance … more
- Charles River Laboratories (Northridge, CA)
- …at HemaCare, you will make a difference every day. **Job Summary** The Associate Director , Technical Excellence is responsible for oversight of Technical ... Services, Donor Ops and PMO. + Responsible, in collaboration with the Director , Manufacturing Operations, and Production Planning to ensure proper staffing capacity… more
- Otsuka America Pharmaceutical Inc. (Richmond, VA)
- The Associate Director , GxP Training, is a critical member of the Learning Center of Excellence within Global Quality. This role is responsible for developing ... and maintaining robust training programs that ensure compliance with Good Practice (GxP) regulations across the organization....+ Ensure all training programs meet global regulatory standards ( FDA , EMA, ICH, etc.) and internal SOPs. + Monitor… more