- J&J Family of Companies (Spring House, PA)
- …more at https://www.jnj.com/innovative-medicine We are currently seeking a motivated Senior Scientist in CMC Regulatory Affairs to join our dynamic team. ... communications in line with global product strategy. + Alert CMC Regulatory Affairs Management to...is eligible to participate in the Company's long-term incentive program . Employees are eligible for the following time off… more
- Takeda Pharmaceuticals (Boston, MA)
- …Proactively recognizes and contributes to enhancing business processes. As part of the Global Regulatory Affairs CMC team, you will report to the Senior ... Director Global Regulatory Affairs CMC . **How you...long-term disability coverage, basic life insurance, a tuition reimbursement program , paid volunteer time off, company holidays, and well-being… more
- Bristol Myers Squibb (Indianapolis, IN)
- …in radiopharmaceuticals . We are seeking an experienced and motivated **Senior Director, Regulatory Affairs - CMC (Manufacturing)** . This position will ... report to the Head of Regulatory Affairs and will oversee and/or manage CMC ...Wellbeing support such as the BMS Living Life Better program and employee assistance programs (EAP). Financial well-being resources… more
- Lilly (Indianapolis, IN)
- …patients who need them all over the world. The Advisor Post approval scientist in Global Regulatory Affairs - CMC Commercial Products will leverage CMC ... around the world. Lilly is looking for post approval regulatory CMC scientists to join us in...individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in… 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 ... for people around the world. Lilly is looking for regulatory CMC scientists to join us in...individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. **Purpose:** The Senior Director of Global Regulatory Affairs - CMC (GRA- CMC ) leads and manages the ... scientific and regulatory efforts of the team, overseeing CMC regulatory activities for global submissions and interactions with regulatory authorities… more
- Lilly (Indianapolis, IN)
- …need them all over the world. The Senior Advisor/Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral products will use ... around the world. Lilly is looking for post approval regulatory CMC scientists to join us in...individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in… more
- Lilly (Indianapolis, IN)
- … CMC technical knowledge and regulatory science expertise to drive regulatory CMC strategies and develop submissions for marketing authorizations for the ... development strategies and submission content + Makes risk-based decisions on CMC regulatory strategies impacting product submissions across geographies and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …as follows: + Champions, independently develops and leads the execution of regulatory CMC investigational and/or registration strategies for assigned products as ... guide the team to define and drive strategy for CMC regulatory dossier content and reviews this...long-term disability coverage, basic life insurance, a tuition reimbursement program , paid volunteer time off, company holidays, and well-being… more
- Lilly (Indianapolis, IN)
- …the world. The Sr. Principal Scientist **or** Advisor Post Approval Scientist in Global Regulatory Affairs - CMC Commercial Products will leverage CMC ... life better for people around the world. Lilly is looking for post approval regulatory CMC (Chemistry, manufacturing and controls) scientists to join us in… more
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