- Lilly (Philadelphia, PA)
- …and advance care for patients with unmet needs. **Position Overview:** The Associate Director , CMC Development will be responsible for the execution ... of multiple radiopharmaceutical CMC development and manufacturing programs supporting various...risks and associated mitigation plans; ensure timely communication with senior management and across relevant functional areas. + Support… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …alongside some of the brightest minds in biopharma. **Position Summary** The Scientific Director / Senior Director , CMC Team Leader is responsible ... into medicines. **This role may be appointed at the Director or Senior Director level.... development and a proven track record in CMC development and/or leading CMC … more
- Lilly (Indianapolis, IN)
- …solutions to support communities through philanthropy and volunteerism. **Position Summary:** The Senior Director , CMC Project Management will provide ... therapeutic areas to translate clinical, asset and portfolio strategy into clear CMC development and delivery goals for cross-functional CMC teams. + Lead… more
- Lilly (Indianapolis, IN)
- …to patients who need them all over the world. The Senior Advisor/ Director in Global Regulatory Affairs - CMC Pre-approval Small Molecules will leverage ... based upon global regulatory changes. + Provide regulatory guidance to allow CMC development teams to make well-informed decisions on development or product… more
- Lilly (Indianapolis, IN)
- …a proactive leadership role in the critical review of molecule specific CMC development strategies and submission content for registration, post-approval ... life-changing new medicines to patients who need them all over the world. The Senior Advisor/ Director Post approval scientist in Global Regulatory Affairs - … more
- Bristol Myers Squibb (Indianapolis, IN)
- …the global leader in radiopharmaceuticals . We are seeking an experienced and motivated ** Senior Director , Regulatory Affairs - CMC (Manufacturing)** . This ... and Marketing Authorization Application (MAA) submissions + Lead the development and execution of global CMC regulatory...care resources. Other perks like tuition reimbursement and a recognition program. If you come across a role that… more
- Lilly (Indianapolis, IN)
- …The Associate Director , CMC Project Management may also partner with the Senior Director or Assoc. VP, CMC Project Management to deliver high ... P2 in the new role. **Position Summary:** The Associate Director , CMC Project Management will provide strategic...and translate clinical, asset and portfolio strategy into clear CMC development and delivery goals for cross-functional… more
- J&J Family of Companies (Horsham, PA)
- …submission. Johnson & Johnson Innovative Medicine R&D is recruiting for a Director , CMC (Chemistry, Manufacturing and Controls) Regulatory Affairs Biologics New ... Spring House, PA; Titusville, NJ; or Raritan, NJ. The Director , CMC Regulatory Affairs Biologics New Modalities...CMC regulatory professionals and will be responsible for development , implementation, and maintenance of global CMC … more
- Takeda Pharmaceuticals (Boston, MA)
- …part of the Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC . **How you will contribute:** + ... therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you...oversee the development and execution of regulatory CMC development and registration strategies. You will… more
- AbbVie (North Chicago, IL)
- …experience; PhD Degree with at least 12+ years of relevant experience. + CMC development experience through IND and/or NDA/MAA. Experience leading multiple ... and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Pharma Product Group Director will be fully responsible for providing CMC leadership and… more