- Takeda Pharmaceuticals (Boston, MA)
- …inspire you and empower you to shine? Join us as a Executive Medical Director , Oncology Clinical Sciences in our Cambridge office. At Takeda, we are transforming the ... development plan that is competitive and consistent with the latest regulatory requirements, proactive identification of challenges, and development of contingency… more
- Abbott (Alameda, CA)
- …**Required Qualifications** + Bachelor's or Master's degree in Engineering, Life Sciences, Regulatory Affairs or a related field or equivalent combination of ... colleagues serve people in more than 160 countries. **Associate Director , Complaint Handling** **Working at Abbott** At Abbott, you...also have access to: + Career development with an international company where you can grow the career you… more
- City of New York (New York, NY)
- …Department of Design and Construction, Division of Public Buildings, seeks an Executive Director to ensure efficient day to day operations of the Public Buildings' ... be responsible with overseeing Public Buildings Program Administration and Regulatory Units, review, prioritize, and coordinate interagency reviews and approvals… more
- Danaher Corporation (Sunnyvale, CA)
- …core team stakeholders such as Project Management, Portfolio Management, R&D, Quality, Regulatory , and Clinical Affairs . The essential requirements of the job ... Danaher Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Director , Product Management, Innovation is responsible for bringing Cepheid's… more
- US Tech Solutions (IL)
- …governance milestones. o Coordinate cross-functional teams, including clinical development, medical affairs , market access, regulatory , and commercial, to align ... **Job Summary:** We are seeking an experienced and motivated HEOR Strategy Associate Director to join our Parkinson's Disease team. You will lead HEOR strategy and… more
- Jabil (Hunt Valley, MD)
- …programs are maintained. + Collaborate with colleagues in Research & Development, Regulatory Affairs , Quality Assurance, and external partners and vendors or ... or established in the laboratory conform to current and appropriate scientific and regulatory standards are suitable for use for their intended purpose. + Develop… more
- Takeda Pharmaceuticals (Boston, MA)
- …processes and training and ensure alignment with global processes and regulatory requirements and expectations. + Drive the implementation and change management ... enable execution of CPMQ activities, ensuring alignment with global processes and regulatory requirements. + Create and deliver training solutions to support the… more
- Veralto (Grand Rapids, MI)
- …Environmental Science, or a related field. A Master's degree or certifications in regulatory affairs is a plus.; applicable to the above stated expectations ... Senior Director of Global Engineering, Quality & Compliance,the **Global Regulatory Compliance Manager** will oversee and manage all regulatory compliance… more
- Mallinckrodt Pharmaceuticals (St. Louis, MO)
- …of 15 years of pharmacuetical industry experience in a Quality Assurance and/or Regulatory Affairs function including experience in manufacturing and control of ... + Minimum 5 years managerial experience in a pharmaceutial quality/ regulatory affairs environment. Preferred Skills/Qualifications: + Previous experience… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Neuropathic Pain, Neuroscience, Neuroscience Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance, Regulatory Compliance,… more