- Fujifilm (Holly Springs, NC)
- …to ensure the systems are properly qualified and validated per standards and regulatory requirements (eg, Food & Drug Administration (FDA)) * Reads piping ... and reviewing documents. This role ensures equipment and systems comply with regulatory requirements and quality standards while ensuring a successful integration of… more
- Genentech (South San Francisco, CA)
- …The ideal candidate will have extensive experience in late stage drug development and managing large-scale clinical trials, including outcoming studies. The ... have strong collaboration with cross-functional teams, including clinical research, regulatory affairs, and product development, to ensure the successful progression… more
- Lilly (Indianapolis, IN)
- … Drug /clinical development experience (for example, epidemiology, toxicology, pharmacology, regulatory affairs, medical affairs) If experience is either in 2 and ... teams in new product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or… more
- Drug Enforcement Administration (Arlington, VA)
- …Planning and Resources Section, Liaison Section, Policy Section, and the Regulatory Drafting and Policy Support Section. Responsibilities Ensures the evaluation of ... procedures and policies for large-scale, national, and international enforcement and regulatory investigations. Meets or designates staff to meet with key officials… more
- Howard University Hospital (Washington, DC)
- …, you will: Reviews pharmacy and organizational policies and procedures in regard to drug use and departmental readiness for regulatory audits. Serves as a ... University Hospital including clinical guidelines, critical pathways, disease management, and drug use programs. Assists in the preparation and presentation of other… more
- Amgen (Thousand Oaks, CA)
- …Let's change the world! As part of Amgen's Process Development organization, Drug Product Technologies (DPT) is seeking a highly motivated **Senior Engineer** to ... role in bringing a wide variety of high-quality clinical and licensed drug products to patients through demonstrated excellence in aseptic processing, technology… more
- Lilly (Indianapolis, IN)
- …Lilly in external forums where standards, common protocols, assessment instruments, regulatory standards and clinical guidelines concerning drug development ... preparation of regulatory reports, including INDs, FDA annual reports, regulatory responses and Periodic Adverse Drug Experience Reports (PADERS),… more
- Genentech (Boston, MA)
- …The ideal candidate will have extensive experience in late stage drug development and a demonstrated level of collaboration experience with cross-functional ... requires a strong understanding of cardiovascular diseases, clinical trial protocols, regulatory requirements, and possibly interactions with regulatory agencies… more
- NRG Energy, Inc. (UT)
- …a culture of accountability. This role ensures compliance with both regulatory requirements and internal standards through risk assessments, monitoring, training, ... policies, procedures, and controls that are specifically tailored to meet regulatory requirements and align with internal business standards, ensuring adaptability… more
- Merck (Rahway, NJ)
- …In summary, our team enables the translation of preclinical candidates into non-oral drug products. We are seeking a highly motivated candidate for the position of ... Principal Scientist (R5) focused on developing parenteral drug products across a range of modalities (small molecule, peptides, proteins, antibody- drug … more