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Your search generated 194 results

Director, Labeling

Cambridge, Massachusetts

Sarepta Therapeutics

Why Sarepta? Why Now? The promise of genetic medicine has arrived, and Sarepta is at the forefront. We hold leadership positions in Duchenne muscular dystrophy (DMD) and limb-girdle muscular dystrophies (LGMDs), and we currently have more t...

Job Type Full Time
MetroPlus Health Plan

Senior Director of Regulatory Affairs

New York, New York

MetroPlus Health Plan

Senior Director of Regulatory Affairs Job Ref: 112166 Category: Professional Department: OFFICE CORPORATE COMPLIANCE Location: 50 Water Street, 7th Floor, New York, NY 10004 Job Type: Regular Employment Type: Full-Time Hire In Rate: $190,00...

Job Type Full Time
Sysmex America, Inc

Sr. Director, Regulatory Affairs

Lincolnshire, Illinois

Sysmex America, Inc

Sr. Director, Regulatory Affairs Job Location(s) US-IL-Lincolnshire # of Openings 1 Job ID 2024-4181 Category Surgical Robotics Business Travel 25% Overview Find a Better Way... ...to use your skills and experience. This is the time to let ...

Job Type Full Time
Meitheal Pharmaceuticals

Head of Global Medical Affairs

Chicago, Illinois

Meitheal Pharmaceuticals

Apply Description About Us: Founded in 2017 and based in Chicago, Meitheal is focused on the development and commercialization of generic injectable medications and, as of 2022, has expanded its focus to include fertility, biologic, and bra...

Job Type Full Time
Comerica Bank

RPO Workstream Lead Senior

Dallas, Texas

Comerica Bank

RPO Workstream Strategy Lead Sr Summary: The Workstream Strategy Lead Sr will be part of the bank's Remediation Program Office ("RPO") and report directly to the Director, RPO, who reports into the Chief Administrative Officer of Comerica. ...

Job Type Full Time
Novartis Group Companies

Regulatory Affairs Executive Director

East Hanover, New Jersey

Novartis Group Companies

Job Description SummaryThe Executive Global Program Regulatory Director (Exec GPRD) provides expert global regulatory leadership throughout the lifecycle of an exceptionally complex project or a portfolio, requiring advanced expertise to na...

Job Type Full Time
Akebia Therapeutics

Sr. Director, Regulatory Affairs - CMC

Cambridge, Massachusetts

Akebia Therapeutics

Sr. Director, Regulatory Affairs - CMC LinkedIn Twitter Email Message Share CMC / Technical Operations Cambridge, MA * ID: 25R-19 * Full-Time/Regular Nearly 37 million Americans are currently affected by Chronic Kidney Disease. 37 million. ...

Job Type Full Time
Incyte Corporation

Associate Director, Global Regulatory Affairs

Wilmington, Delaware

Incyte Corporation

Overview Incyte is a biopharmaceutical company focused on the discovery, development, and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity. Incyte is committed to the rig...

Job Type Full Time
Blueprint Medicines

Director, Process Chemistry

Cambridge, Massachusetts

Blueprint Medicines

How will your role help us transform hope into reality? As a recognized expert in drug substance development and manufacturing, you will enable advancement of Blueprint Medicines' clinical and commercial programs. You will be expected to co...

Job Type Full Time
PTC Therapeutics, Inc

Contract, Global Regulatory Affairs CMC Fellow (Warren, NJ - Hybrid)

Boston, Massachusetts

PTC Therapeutics, Inc

PTC Therapeutics is a global commercial biopharmaceutical company. For over 25 years our team has been deeply committed to a unified purpose: Extending life's moments for children and adults living with a rare disease. At PTC, we cultivate ...

Job Type Full Time

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