- GE HealthCare (Chicago, IL)
- …**Roles and Responsibilities** + Executes against the Quality & Regulatory Business Development Process. This includes scheduling, preparation, execution, reporting, ... and ensuring strategy is executed to current industry practices and regulatory expectations. + Standardization of processes, tools, and performance management… more
- System One (Alameda, CA)
- Job Title: Senior DMPK Director ( Drug Metabolism & Pharmacokinetics) Location: Alameda , California Type: Direct Hire Compensation: $242000 - $278000 annually ... to development stage and build comprehensive DMPK packages to enable successful drug registration. The senior director is responsible for providing strategic… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …Gilead and help create possible, together. **Job Description** **POSITION OVERVIEW:** Regulatory Affairs (RA) Business Operations believe talented people deserve a ... Management + Change, Communications and Engagement + Performance Management + Regulatory Inspection and Standards Excellence (RISE) Management + Business Process… more
- Fujifilm (Holly Springs, NC)
- **Position Overview** ** Director , QA Drug Substance Operations** Are you a strategic leader with expertise in managing teams of QA professionals and ... and grow in a world-class Quality organization as the Director , QA Drug Substance Operations. In this...quality systems that align with CGMP, GDP, and other regulatory standards, ensuring product compliance through robust quality systems.… more
- Bristol Myers Squibb (Devens, MA)
- …in their personal lives. Read more: careers.bms.com/working-with-us . Position: Executive Director , Biologics Drug Substance, Manufacturing Sciences & Technology ... Join us and make a difference. Position Summary The Head of Biologics Drug Substance Manufacturing Sciences & Technology is responsible for scientific and technical… more
- Danaher Corporation (Fargo, ND)
- …safeguard and improve human health. We are seeking a strategic and technically accomplished Director of Drug Product CMC to lead client-facing drug product ... sequence to vial mRNA services. A key responsibility will be to implement drug product strategy across all departments ensuring alignment with overall company goals… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- **Job Summary** **** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes ... review technical reports, protocols, risk assessments, and relevant sections of regulatory submissions (IND, BLA, MAA, etc.) related to downstream processing. +… more
- Gilead Sciences, Inc. (Foster City, CA)
- …**Job Description** **Specific Responsibilities:** The primary responsibility of this Biologics DMPK Director position is to serve as an expert in the PK and ... + Lead the DMPK strategy for programs at various stages of drug discovery/development in collaboration with inter-disciplinary team; champion activities to deliver… more
- JPMorgan Chase (Jersey City, NJ)
- …they have access to the best possible care and resources. As the Executive Director , Prescription Drug lead within the Benefits Department at JPMorgan Chase, you ... will manage and enhance our Prescription Drug offerings and other benefits programs. Your role will...prescription drugs, dental and vision + Monitor legislative and regulatory changes to ensure compliance with new and existing… more
- Lilly (Indianapolis, IN)
- …has a diverse and expanding portfolio of ADCs that require thorough drug -linker process development and regulatory submission strategies, often with compressed ... accelerate the development of lifesaving new medicines for our patients. Our antibody- drug conjugate (ADC) team seeks to perform innovative and cutting-edge research… more