- Teva Pharmaceuticals (Salt Lake City, UT)
- …environment, Supply Chain or Materials Management. * Requires strong knowledge of pharmaceutical materials and general manufacturing processes. * Requires ... Senior Director , Supply Chain & Planning Date: Aug 22,...industry regulatory requirements as they relate to the production of pharmaceutical products and associated quality systems.… more
- Lilly (San Diego, CA)
- …Committee on Medical Education (LCME). **Preferred Qualifications** + Minimum 3-5 years of pharmaceutical industry experience in clinical development + PhD in ... those who need them, improve the understanding and management of disease, and give back to our communities through...physician scientist to join our Immunology team as Medical Director , Early Clinical Development. This role is designed for… more
- Novo Nordisk (Washington, DC)
- …strongly preferred + Demonstrated career progression with increasing roles of responsibility + Pharmaceutical /healthcare industry experience and knowledge ... ready to realize your potential? The Position The Senior Director works on complex issues that require an in-depth...works on complex issues that require an in-depth knowledge of the company and its long-term ambitions. Develops NNI's… more
- Sanofi Group (Morristown, NJ)
- …record with a minimum of 1 year (3+ years preferred) of regulatory experience, preferably within the pharmaceutical /medical device/biotech industry + ... **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location**...scientific subject matter is extremely helpful + Significant understanding of the US pharmaceutical marketplace, especially the… more
- Teledyne (Thousand Oaks, CA)
- …and the aerospace, defense, or commercial aviation industry. + Strong understanding of federal procurement processes and FAR/DFARS compliance . + Domestic and ... oil and gas exploration and production, medical imaging and pharmaceutical research. We are looking for individuals who thrive...thrive on making an impact and want the excitement of being on a team that wins. **Job Description**… more
- Cambrex High Point (Charles City, IA)
- …Start a career where You Matter by applying today! Job Overview The Associate Director of Capital Projects is responsible for the strategic planning, execution, ... in this section may be assigned. Qualifications/Skills + Strong knowledge of GMP regulations, validation practices, and pharmaceutical production processes.… more
- Lilly (Indianapolis, IN)
- …multi-organizational environment while maintaining prioritization and ensuring appropriate level of compliance with policies and procedures. **Basic ... medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.… more
- Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
- …This role is responsible for ensuring the robustness, scalability, and compliance of downstream operations through effective technology transfer, validation ... **Job Summary** **** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing processes… more
- Otsuka America Pharmaceutical Inc. (Augusta, ME)
- …skilled and experienced professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. ... This role is responsible for ensuring the robustness, scalability, and compliance of upstream operations through effective technology transfer, validation… more
- BeOne Medicines (Pennington, NJ)
- **General Description:** We are seeking a strategic and detail-oriented Director of Inventory and Cost Accounting to oversee our global inventory valuation and ... + Monitor and ensure adherence to internal and external compliance (eg SOX) related to inventory and costing controls.... accounting/financial experience with at least 8 plus years of relevant finance experience in the pharmaceutical … more