- Charles River Laboratories (Shrewsbury, MA)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... management, interpretation, and reporting of study data and assuring the regulatory compliance of these projects, as appropriate. Additional responsibilities include… more
- Charles River Laboratories (Reno, NV)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... inspections of routine processes to assure compliance with applicable regulatory requirements, international standards, and corporate policies and procedures. This… more
- AbbVie (North Chicago, IL)
- …of analytical scientists supporting early phase development of New Chemical Entities (NCEs) drug substance and drug product in both preclinical and clinical ... programs. The candidate should have extensive expertise in applying regulatory guidelines within an R&D environment with a fit for purpose mind set. The candidate… more
- Otsuka America Pharmaceutical Inc. (Atlanta, GA)
- …of drugs and unmet medical needs. + Formulating a rationale to develop the drug in accordance with a clinical and regulatory strategy. + Working with ... position requires deep understanding of all aspects of the drug development process from early clinical stages to post...with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible… more
- Pfizer (Groton, CT)
- …vaccines that matter most. Whether you are in the discovery sciences, ensuring drug safety and efficacy or supporting clinical trials, you will apply cutting edge ... accelerate and bring the best-in-class medicines to patients around the world. The Drug Product Analytics group is accountable for the analytical aspects of drug… more
- Beth Israel Lahey Health (Cambridge, MA)
- …work experience strongly preferred. * Strong working knowledge of brand and generic drug names and basic pharmacology. * Basic familiarity with computers. Ability to ... department. 32. Evaluates departmental and hospital policy and practice compliance with regulatory agencies (eg, Joint Commission) as well as state and federal laws,… more
- WMCHealth (Warwick, NY)
- …and storing medications and controlled substances and other applicable regulatory requirements including 340B and USP797 compliance. The Pharmacist provides ... on specified target drugs and initiates pharmacokinetic dosing protocols. Evaluates drug therapy for appropriateness and makes drug therapy recommendations… more
- Lilly (Indianapolis, IN)
- …teams to develop robust control strategies for drug substances and drug products, enable clinical programs, and author regulatory submissions. + Drive ... Design and Development (SMDD) organization is responsible for the development of synthetic drug substances and drug products from the pre-clinical phase through… more
- Bristol Myers Squibb (Cambridge, MA)
- …of a global integrated program strategy from candidate nomination through drug development to successful launch and commercialization. The GPL develops, leads, ... **Technical/Functional Responsibilities:** **Develops and manages product strategy and late drug development program to ensure approval and commercial success** +… more
- Sutter Health (Oakland, CA)
- …Performs billing, pricing, record keeping, and provision of services required to meet regulatory requirements. + Maintains records of drug distribution and works ... role involves a fast-paced environment with an emphasis on compliance and regulatory standards in patient care and medication management. **PHARMACY SERVICES** +… more