- Lilly (Indianapolis, 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 Small Molecule Process Engineering provides leadership and direction to… more
- Takeda Pharmaceuticals (Boston, MA)
- …care decision-makers to guide HE strategies Communication/Publication: + Ensure the drug 's value proposition will be recognized among the external (scientific/ payer ... Access, Global Evidence and Outcomes, Medica Affairs, Clinical Development, Regulatory Affairs, Biostatistics, Global Emerging Markets (GEM; eg, China), Project… more
- Rhythm Pharmaceuticals (Boston, MA)
- …adapt, learn, and our tenacity to overcome barriers, together. Opportunity Overview The Sr. Associate , Analytical Chemistry will be a member of the Tech Ops team and ... of testing performed at Rhythm's contract sites for the manufacturing and testing of Drug Substance and Drug Product. This position will s upport analytical… more
- Teleflex (Minneapolis, MN)
- Clinical Research Associate Manager (REMOTE) **Date:** Nov 20, 2025 **Location:** Minneapolis, MN, US **Company:** Teleflex **Expected Travel** : More than 50% ... now also includes Passeo (TM) -18 Lux (TM) Peripheral Drug -Coated Balloon Catheter, Pantera (TM) Lux (TM) Drug...* Train site personnel regarding the protocol and applicable regulatory requirements. * Ensure each site is meeting its… more
- Mizuho Corporate Bank (New York, NY)
- …potential risk to the firm + Ability to determine and review Dodd Frank regulatory information provided by the client and determine if sufficient based on regulation ... all documentation required to adhere to both AML and regulatory requirements + Liaise with internal groups such as...We participate in the E-Verify program. We maintain a drug -free workplace and reserve the right to require pre-… more
- Lilly (Pleasant Prairie, WI)
- …programs as needed. Additionally, this role will act as an IH/HSE regulatory advisor for manufacturing and support units, ensuring ongoing compliance and fostering ... and submitted on time, incorporating second person verification as needed. + Regulatory Guidance: Be a resource to operational areas, helping them understand the… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** **Come join our team!** The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, ... conduct research participant visits independently. + Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB). May work directly… more
- Lilly (Indianapolis, IN)
- …around the world, and emphasizing emerging, innovative technologies in both Drug Product and Biotech platforms utilizing advanced data and process control ... as Global Facilities Delivery (GFD) and Global Quality. **Responsibilities:** The Associate Director - Global Process Automation & Control Engineering position has… more
- The Boeing Company (Berkeley, MO)
- …programs in **Berkeley, MO** or **Hazelwood, MO** . We are seeking an ** Associate (Level 2), Mid-Level (Level 3), or Senior (Level 4) Aircraft Safety Engineer** ... validation and verification activities in compliance with relevant customer and regulatory safety standards + Supports creating and maintaining safety and corrective… more
- The Boeing Company (Smithfield, PA)
- …to safety and quality standards, ensuring that all operations meet regulatory compliance and operational excellence. If you are detail-oriented, possess strong ... for a broad range of experience levels including : Associate and Mid Level Manufacturing Assemblers. **Position Responsibilities** +...order to attain higher levels of performance **Travel** **10%** ** Drug Free Workplace** Boeing is a Drug … more