- ZOLL Medical Corporation (Boston, MA)
- …career. Job Overview: ZOLL Medical Corporation is seeking a Professional Relations Director to lead and manage relationships within the cardiac health sector. This ... in the cardiac care space . The Professional Relations Director will play a key role in driving ZOLL's...promotes ZOLL's technologies through digital platforms and social media. Compliance & Budget Management : + Ensure all professional… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and Promotion (GRA A&P) Review Lead is ... prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead you will act as… more
- Rhythm Pharmaceuticals (Boston, MA)
- …and our tenacity to overcome barriers, together. Opportunity Overview The Associate Director (AD) of Regulatory Operations is responsible for assisting the Head of ... quality, accuracy, and adherence to regulatory guidelines. Additionally, the Associate Director supports the preparation and submission of Investigational New Drug… more
- AmeriHealth Caritas (Southfield, MI)
- …We're looking for the next generation of health care leaders. Responsibilities: The Director of Contract Performance reports to the Market President and must serve ... two days in the Southfield, MI office.; ; **Key Responsibilities** + The Director of Contract Performance is responsible for developing systems and tools to ensure… more
- Rhythm Pharmaceuticals (Boston, MA)
- …our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you will be responsible for ensuring the ... the effective management and timely execution of regulatory filings, maintaining compliance with global regulatory standards and commitments. You will provide… more
- Merck (West Point, PA)
- **Job Description** Our company's Pharmaceutical Sciences and Clinical Supply (PSCS) organization translates molecules to medicines, working from the discovery ... Manufacturing Organizations (CMOs) conducted by project managers + Provide manufacturing and compliance expertise to project teams and junior ExDM members + Identify… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Description:** The role of Associate Director of US Commercial Regulatory Affairs requires the ability to apply ... Promotion advisory submissions and sub part e submissions + Ensure full regulatory compliance of all promotions with approved labeling and /or FDA guidances + Ensure… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Director , Global Regulatory Labeling Strategy where you will be responsible for the ... EU SmPC enabling the most up-to-date information and in compliance with labeling requirements to be provided to patients...(MSc, PhD, or PharmD) preferred. + 10+ years of pharmaceutical industry experience. This is inclusive of 8 years… more
- Sysco (Rahway, NJ)
- …a high-performing quality culture across the organization. **POSITION PURPOSE:** The Director of Global Quality Assurance & Quality Control leads the quality ... System (QMS) that ensures product excellence, customer satisfaction, regulatory compliance , and business continuity across the entire supply chain-from development… more
- GE HealthCare (Chicago, IL)
- …activities; identification and communication of high-risk issues; reporting compliance concerns and recommended improvements to business leadership; developing ... of 7 years' experience in the medical device or pharmaceutical industry; or Bachelor's Degree and a minimum of...5 years' Experience driving Global programs to resolve quality compliance issues (directly). + Experience with Pharma QMS requirements… more