- System One (Alameda, CA)
- Job Title: Senior DMPK Director ( Drug Metabolism & Pharmacokinetics) Location: Alameda , California Type: Direct Hire Compensation: $242000 - $278000 annually ... develop and implement DMPK and modeling & simulation strategies to advance drug candidates from discovery to development stage and build comprehensive DMPK packages… more
- HCA Healthcare (Mckinney, TX)
- …and dispense pharmaceuticals + Complies with facility policy and procedures and regulatory requirements + Monitor drug therapy regimens for contraindications, ... cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free...Maintain appropriate controlled substance records + Comply with all regulatory standards Prioritize work and lead others to comply… more
- Sanofi Group (Cambridge, MA)
- …Ready to get started? **Main Responsibilities** + Develops medical devices and drug device combination products following regulatory requirements (FDA, EU MDR) ... responsibility for ensuring robust device design and successful delivery of Drug Device Combination Products and Medical Devices. Working within strict technical,… more
- Catalent Pharma Solutions (Philadelphia, PA)
- …or biotech firms preferred. + Experience working with global supply chains and regulatory compliance in drug sourcing preferred. + Bachelor's degree in science, ... Business Development Manager to lead the sales of our Drug Comparator Services. In this role, you will be...terms. + Stay up to date on industry trends, regulatory requirements, and competitor activities. Identify emerging opportunities in… more
- Sanofi Group (Cambridge, MA)
- …project team and internal partners such as clinical operations, translational medicine, regulatory affairs, biostatistics, drug discovery, drug safety, ... clinical sections of integrated development plans, and submission dossiers for regulatory approval + Support drug registrations (contribution to submission… more
- University of North Carolina- Chapel Hill (Chapel Hill, NC)
- …specimen banking, clinical trials design, clinical trials data management, and new drug and laboratory testing regulatory affairs. Additionally, as the direction ... the current/projected fiscal environment. They will ensure grant financial and regulatory compliance, manage contracts and subawards and supervise financial staff.… more
- Contract Pharmacal Corp (Hauppauge, NY)
- …and troubleshooting. + Stays current with recent advances and trends in the drug delivery technology and regulatory policies. + Other responsibilities as ... is primarily responsible for the formulation product development and submission of regulatory documents for oral solid dosage and other pharmaceutical dosage form.… more
- Amgen (Washington, DC)
- …analysis plans, and clinical study reports + Prepare/review safety sections of new drug applications and other regulatory filings + Serve as safety expert ... **Preferred Qualifications:** + Product safety in the bio/pharmaceutical industry or regulatory agency + Previous management and/or mentoring experience + Experience… more
- Bristol Myers Squibb (Devens, MA)
- …Read more: careers.bms.com/working-with-us . Position: Executive Director, Biologics Drug Substance, Manufacturing Sciences & Technology Location: Devens, ... 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)
- …human health. We are seeking a strategic and technically accomplished Director of Drug Product CMC to lead client-facing drug product development and ... 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