- Sumitomo Pharma (St. Paul, MN)
- …a dynamic, highly motivated, and experienced individual for the position of **Associate Director , Regulatory Affairs (Oncology).** The Associate Director ... is part of the Global Regulatory Affairs (GRA) team based in the US. He/She will...Ideally with a minimum of 4 years focused in regulatory affairs + Oncology product development experience… more
- Sumitomo Pharma (St. Paul, MN)
- …are currently seeking a dynamic, highly motivated, and experienced individual for the position of ** Director Regulatory Affairs ** . The Director is part ... of the Global Regulatory Affairs (GRA) team based in the US. He/she will...pharmaceutical industry with minimum of 8 years focused in regulatory affairs . + Master's degree required (preferably… more
- United Therapeutics (St. Paul, MN)
- …or pharma regulatory experience with a Bachelor's Degree in life sciences, quality, regulatory affairs or a related area of study or 10+ years of biologic ... pharma regulatory experience with a Master's Degree in life sciences, quality, regulatory affairs or a related area of study or 7+ years of biologic or… more
- Merck (St. Paul, MN)
- **Job Description** + The Precision Medicine - Medical Affairs Director - Health Systems Oncology (PM MAD-HSO) develops ongoing professional relationships with ... account plans in partnership with Precision Medicine Health Systems Oncology Medical Affairs Director (PM HSO-MADs), oncology account management, and precision… more
- WelbeHealth (St. Paul, MN)
- …stakeholders. **Essential Job Duties:** + Lead the WelbeHealth federal legislative and regulatory affairs function with Congress and the Centers for Medicare ... providing an all-inclusive care option to our most vulnerable senior population. The Director , Federal Government Affairs will lead a bold advocacy strategy to… more
- Medtronic (Mounds View, MN)
- …Affairs Specialist** to join the CAS Medical Science team, reporting to the Director of Medical Affairs to assist in the acquisition, assimilation, and ... dissemination of clinical evidence for aortic therapies. The Medical Affairs team evaluates the evidence landscape to tell a clinical story grounded in evidence with… more
- Danaher Corporation (New Brighton, MN)
- … compliance. This position reports to the Director of Quality Assurance and Regulatory Affairs and is part of the Quality Assurance and Regulatory ... progressive experience in operations quality assurance, with exposure to QMS and regulatory affairs in regulated industries (eg, medical device, pharmaceutical,… more
- Minnesota State (St. Paul, MN)
- …Date (if designated).** **Working Title:** Systems Analysis Unit Supervisor - Director of Data Services and Institutional Analytics **Institution:** Saint Paul ... **Salary Range:** $38.74 - $66.92 **Job Description** **Job Summary:** The Director of Data Services and Institutional Analytics provides leadership and oversight… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …, legal, and ethical guidelines + Foster strong partnerships with Medical Affairs , Clinical Development, Market Access, Market Research, Regulatory , Legal, and ... our focus to ultra-rare neurological conditions. **Job Summary** The Executive Director , Sales and Marketing, Neurology Rare Disease will be responsible for… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …cross-functionally with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to ... **Associate Director , Small Molecule Analytical Development** + Lead and...and drug product ensuring compliance with relevant ICH and regulatory guidelines + Develop and implement stability study protocols… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- **Position Summary:** The Director GVE Operations oversee and coordinates projects within the department to ensure alignment with organizational goals. This role is ... other integrated data generation initiatives. This position reports to the Senior Director , Global Integrated Evidence & Innovation Operations and can be based in… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …appropriate. + Collaborate with cross-functional teams including R&D, Quality Assurance, Regulatory Affairs , and Operations to align strategies and optimize ... **Position Overview:** The Senior Director , MSAT Biologics provides strategic and technical leadership...validation lifecycle (PPQ, CPV, etc.) ensuring compliance with global regulatory standards. + Establish and oversee robust Continued Process… more
- 3M (Maplewood, MN)
- **Job Description:** ** Director , Assistant General Counsel - Corporate & Securities** **Collaborate with Innovative 3Mers Around the World** Choosing where to start ... statements (WKSI S-3 shelf; S-4; S-8); and emerging areas such as ESG regulatory disclosures. + Corporate governance experience - working closely with the Corporate… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- …data scientists and data programmers, and external stakeholders including Medical Affairs , Value and Real World Evidence to provide end-to-end statistical expertise ... approve tables, listings and graphs specifications. + Closely work with Medical Affairs to support statistical design, conduct secondary analyses of clinical and… more
- Prime Therapeutics (St. Paul, MN)
- …Sr Dir Pharmacy Trade Relations - Remote **Job Description** The Sr Director , Pharmaceutical Trade Relations is responsible for managing Prime's Trade Relations ... on Medicare Part D and Managed Medicaid. The Sr Director , Pharm Trade Relations leads a team of directors...needs in rebate contracting. + Serve as a government affairs expert including providing support to Prime's gov't … more
- Medtronic (Mounds View, MN)
- …and development opportunities + Partner with marketing, geographies, clinical, legal, regulatory affairs , packaging and labeling, sales force, supply chain, ... Communications processes. This role will report to the Senior Director of CV Technical Communications. **Role and responsibilities:** +...documentation control, translation teams, regulatory agencies, etc. in support of both the CRDN… more