- Lilly (Indianapolis, IN)
- …program ownership for key programs across the corporation. **Position Overview:** The Associate Director - Corporate Mechanical Disciplines position has overall ... supporting the overall corporate design, delivery, and equipment strategies. The Associate Director role will provide mechanical engineering discipline… more
- Curia (Albuquerque, NM)
- Associate Director , Automation Engineering in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract ... matching contributions + Learning platform + And more! The Associate Director of Automation Engineering is responsible...Demonstrates strong attention to detail + Detailed Knowledge of cGMP and regulatory requirements relating to process … more
- Merck (Rahway, NJ)
- … Principal Scientist - Device Technical and Engineering Lead ( Associate Director Equivalent)** _Our company's Device Product & Process Development (DPPD) ... position will be responsible for applying their knowledge of product and process development in the (bio)pharmaceutical and/or medical device industries to set… 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 ... current Good Laboratory Practice (cGLP) and current Good Manufacturing Practice ( cGMP ) compliant Cell & Gene Therapy (C>) products.. Essential Responsibilities +… more
- Boehringer Ingelheim (St. Joseph, MO)
- …for the company + Continuous improvement by the reduction of equipment and process failures + Define and Drive Strategy: + Identification of new applicable ... it + Responsible for governance framework, automation guidelines and approval process **Requirements** + Bachelor's degree in Engineering, Maintenance or related… more
- Merck (Rahway, NJ)
- …safety, quality, and equipment decisions. This role evaluates safety, product/ process quality, and equipment performance and determines the appropriate path ... on next steps, including stop‑work when risk warrants; escalate and document per cGMP expectations. + Serve as owner and trainer for key equipment with emphasis… more
- Lilly (Indianapolis, IN)
- …mentoring to drive analytical initiatives and improvements. The Quality Control (QC) Associate Director (AD) Analytical Sciences is responsible for leading the ... but not limited to analytical stewardship, chromatography, Mass Spectroscopy, and Process Analytical Technology. + Provide leadership and oversight for method… more
- Lilly (Indianapolis, IN)
- …world. Eli Lilly and Company is seeking an experienced and highly motivated Associate Director to join our Technical Services/Manufacturing Science (TS/MS) team, ... robust and compliant manufacturing of peptide drug substances, from process development through commercialization and life cycle management. **Job Responsibilities**… more
- Merck (West Point, PA)
- …responsibility for microbial control and sterility assurance related topics. In the Associate Director role, the incumbent will provide subject matter expertise ... maintaining the divisional quality standards in alignment with regulatory requirements, cGMP expectations, and industry trends + Assisting manufacturing sites and… more
- Merck (Rahway, NJ)
- **Job Description** The Biologics Process Research & Development organization within our Company Research Labs is responsible for developing the drug substance ... material to supply clinical trials. We are also responsible for commercial process development, and development and implementation of new technologies. We work with… more