- Lilly (Durham, NC)
- …to make life better for people around the world. The Associate Director - Quality Engineering is responsible for demonstrating leadership, teamwork, and quality ... and regulatory knowledge to lead the Quality Engineering team to...vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (eg, healthcare and/or dependent day… more
- WSP USA (Raleigh, NC)
- This Opportunity WSP is currently initiating a search for a **Senior Technical Director , NCDOT Client Manager** in our **Raleigh, NC** office. This role provides ... Federal, State, and Local engineering/design/construction laws, codes, policies, and regulatory requirements. + Oversee internal vision and mission for the… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and ensure Gilead is highly competitive in commercial markets. As the ** Director , Human Factors Engineering and Human-Centered Design Specialist** you will support ... Qualified candidates will focus on the development of devices and drug -device combination products such as pre-filled syringes and auto-injectors. **Specific Job… more
- ARCO (Raleigh, NC)
- …stage of construction? If so, we have an exciting opportunity for you as a Director of Quality Management based in Raleigh, NC. In this senior leadership role, you ... culture that supports diversity and inclusion. We are proud to be a drug -free workplace and an equal opportunity employer, and all qualified applicants will receive… more
- AbbVie (North Chicago, IL)
- …scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. + Oversees the conduct of clinical trials ... documents reporting safety monitoring and other scientific reports submitted to the regulatory authorities. + Participation in design and execution of clinical trial… more
- Bristol Myers Squibb (Boston, MA)
- …the development of immuno-oncology therapies and continues to diversify in drug development for the treatment of cancers. Our world-class Translational Development ... on translational data generated to support asset development and contribute to regulatory submissions. This individual will work on cross-functional project teams to… more
- Lilly (Indianapolis, IN)
- …over the world! **Position Brand Description:** Provides technical leadership for drug product manufacturing processes under development and in commercial production ... sites, and applicable functional areas to commercialize new dry oral solid drug products . + Leverage prior experience to anticipate commercial manufacturing… more
- 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 ... and assignments meet client needs. o Maintain the scientific, safety, and regulatory compliance integrity of the entire bioanalytical process. o Provide hands on… more
- Lilly (Lebanon, IN)
- …the Lilly Medicine Foundry, a new center for advanced manufacturing and drug development. The first-ever facility of its kind, combining research and manufacturing ... trial medicines, while also reducing costs and environmental impact. The Associate Director of Materials will lead the planning and procurement of direct materials… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. **Position Overview:** The Executive Director - Global Imaging Portfolio and Project Management, Global Imaging, will report ... areas such as Clinical Development, Medical, Imaging Operations, Imaging R&D, Regulatory , Business Development, and field medical teams; facilitates effective cross… more