- Lilly (Indianapolis, IN)
- …clinical trial medicines, while also reducing costs and environmental impact. The Associate Director Small Molecule Process Engineering provides leadership and ... influence and implement the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Identify, track, and report key indicators of… more
- Lilly (Houston, TX)
- …a successful startup into GMP manufacturing operations. **Position Overview** The Associate Director - Operational Readiness is a key site leader responsible ... project managers and the Site Lead Team to align all workstream deliverables. The Associate Director ensures clear communication between the GFD project team and… more
- Lilly (Pleasant Prairie, WI)
- …Reporting to the Sr. Director of Supply Chain and Logistics, the Associate Director - Warehouse and Logistics will join leading logistics operations between ... work group / team to attain departmental and site objectives for safety, quality , delivery, cost, and people + Ensure warehouse and logistics teams meet production… more
- Cambrex High Point (Charles City, IA)
- …world. Start a career where You Matter by applying today! Job Overview The Associate Director of Capital Projects is responsible for the strategic planning, ... manufacturing excellence, as well as our strong commitment to quality and safety, we offer a range of career...for capital initiatives. + Ensure all projects comply with GMP , environmental, health and safety (EHS), and regulatory requirements.… more
- Lilly (Indianapolis, IN)
- …for people who are determined to make life better for people around the world. ** Associate Director Global MES - PharmaSuite & PMX** **This is an opportunity you ... You will be part of Tech@Lilly MQ (Manufacturing and Quality ), an organization that drives manufacturing operational excellence and...**What You'll Be Doing** : As the **Global MES Associate Director ,** you will guide a team… more
- Charles River Laboratories (Northridge, CA)
- …at HemaCare, you will make a difference every day. **Job Summary** The Associate Director , Technical Excellence is responsible for oversight of Technical ... research, clinical studies from phases 1 to 3, and commercialization with high- quality RUO and GMP -compliant starting material and apheresis collections. In… more
- Merck (Elkton, VA)
- …**Primary Responsibilities** Reporting to the Director of Operations, the Associate Director is accountable for the oversight of Manufacturing Operations, ... + Ensures staff activities are aligned with department objectives to reliably supply quality product at a competitive cost + Forecasts resource needs and manages… more
- United Therapeutics (Research Triangle Park, NC)
- …individual expertise and mentoring or developing a member of your team. The Associate Director , QA Engineering will provide advanced support and subject matter ... option. **Who You Are** You bring a wealth of Quality Assurance knowledge to the table and are eager...+ Clear understanding of US FDA, EU, and JP GMP regulations + Knowledge of software validation practices and… more
- Lilly (Indianapolis, IN)
- …while also reducing costs and environmental impact. **Position Description:** The Associate Director Operational Readiness is responsible for managing the ... is expansive, stretching across all functional areas of the site, requiring the Associate Director Operational Readiness to build breadth of knowledge and work… more
- Gilead Sciences, Inc. (Foster City, CA)
- …, QA oversight of manufacturing/testing, and independence from production per our GMP Quality Manuals (Gilead/Kite). + Hands-on leadership ensuring **QA ... and help create possible, together. **Job Description** The Senior Director , Quality Assurance leads the site's independent...with 14+ years of experience in Biopharmaceutical or Pharmaceutical quality control OR Associate degree with 16+… more