- Aequor (Seattle, WA)
- …inputting and expressing Quality principles Position Reports to Jenna Walker - Associate Director , QA Training & Document Control Education: Bachelor's degree ... working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …identify process risks and associated critical controls around the associate processing steps Provide mentorship to deviation management team members Acts ... role with relocation assistance eligible for selected candidate.Relationships Reports to: Director of MSAT & Quality Control Number of subordinates with… more
- Merck & Co. (Rahway, NJ)
- …fast-paced job that provides both technical and project management responsibility. The Associate Specialist - Manufacturing Automation position will report to the ... Director , Engineering, Automation Lead position and will be a...production, utility systems and associated infrastructure.- Responsibilities of the Associate Specialist - Manufacturing Automation include the following: Small… more
- Merck & Co. (Durham, NC)
- …to have the safest and most compliant operation around the network.EMSS has an Associate Director opening for the Teknika maintenance and Engineering team. The ... facility. The Teknika Facility handles and End to End process and part of the main equipment includes all...Minimum 8 years of progressive Maintenance leadership experience in cGMP operations (6 Years with a master's degree or… more
- Novo Nordisk Inc. (Boulder, CO)
- …quality, cost & timely completion of all validation deliverables. Relationships Associate Director . Essential Functions Perform, review & approve ... With a new laboratory completed in 2021 to support analytical and process development, the CMC team works alongside Quality, Regulatory, Technical Operations and… more
- University of Southern California (Los Angeles, CA)
- cGMP Associate Director Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... in compliance with current Good Manufacturing Practices ( cGMP ). As the Associate Director of Process Development, the individual will be responsible for… more
- University of Rochester (Rochester, NY)
- …and the Upstate Stem Cell cGMP Facility (USCGF) teams. The QC Associate will be responsible for upholding in- process and final release analysis of ... Responsibilities **Position Summary:** The Quality Control (QC) Associate I will be a member of the...are reported in a timely manner to the QA Director of the cGMP Facility, therefore interacting… more
- BeiGene (Hopewell, NJ)
- **_General Description:_** The Associate Director Site Technical Services is responsible for the day-to-day activities of the Validation team, Metrology, CMMS ... audits and inspections, write and implement Equipment, Facility and Process Installation/Operational/Performance Qualifications (IQ/OQ/PQ), and write deviations, root causes,… more
- Lilly (Indianapolis, IN)
- …people who are determined to make life better for people around the world. The Associate Director , Capital Procurement Process Owner in the Development & ... objectives and maintaining compliance with Procurement practices. Continually drive process improvement across projects using metrics. + Provide strategic insights… more
- Lilly (Indianapolis, IN)
- …quality oversight of Indianapolis Parenteral Manufacturing's central quality processes. The Associate Director for Site Quality & Compliance is responsible ... of quality medicine, strong quality culture and maintenance of cGMP compliance and inspection readiness + Actively assist in...of responsibility + Act as primary back-up for other Associate Directors in Site Quality and Compliance, upon delegation… more
- ARCO (Framingham, MA)
- …**A DAY IN THE LIFE** + Design and manage construction of cGMP manufacturing facilities from concept design to completion, including preconstruction and estimating ... + Assist client by analyzing manufacturing process to develop project performance specifications, space planning, etc....focusing on improvements in safety, quality, and efficiency for cGMP end users + Be a subject matter expert… more
- Lilly (Indianapolis, IN)
- …life better for people around the world. #WeAreLilly **Organization Overview:** The ** Associate Director - Analytical Operations and Compliance** will have ... Our organization is comprised of experienced, creative, and energetic process chemists, analytical chemists, formulation scientists, and engineers who… more
- Lilly (Lebanon, IN)
- …impact to our environment. **What You'll Be Doing** The Manufacturing & Quality (MQ) IT Associate Director -IT for LP1 will be part of the IT Leadership team for ... This role will report to the MQ IT Sr Director for LP1. This role will work hand by...+ Provide leadership in the development and execution of cGMP and/or improvement plans within the IT function and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** **Key Responsibilities** Associate Director , Global External Manufacturing Biologics ensures ... global external contract manufacturing network, while ensuring compliance with cGMP , regulatory requirements, and environmental, health, and safety legislations.… more
- Regeneron Pharmaceuticals (Troy, NY)
- The IT department is hiring! The Associate Director IT Applications - Lab Systems position leads the Global Laboratory Systems team within the Information ... development, maintenance and compliance activities for Laboratory software and process control systems in our QC, Chemistry, Micro and...as Endoscan V, SoftMax Pro and DataPro2. As an Associate Director , a typical day might include… more
- Lilly (Indianapolis, IN)
- …to make life better for people around the world. Responsibilities: The API EM Associate Director (AD) - Quality Control provides analytical leadership for the ... of the regulations applicable to laboratory testing in a cGMP environment. + Identify and resolve laboratory safety issues...to request an accommodation as part of the application process . Any other correspondence will not receive a response.… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …regulated cGMP environment preferably in Biopharmaceuticals / Plasma Fractionation process and its various capacity constraints. + Detailed experience in supply ... and services in more than 110 countries and regions. ** Director ,Supply Chain** The Director , GTI Supply Chain...significant role as it relates to insuring the proper process controls, reports and systems are in place, allowing… more
- Lilly (Lebanon, IN)
- …startup into GMP manufacturing operations. **Position Description:** Reporting to the Senior Director of Operations, Associate Director of the Warehouse ... team of people to operate the state-of-the-art warehouse. The Associate Director of the Warehouse will also...corporate and site goals + Ensure robust inventory management process is developed and maintained + Ensures that all… more
- Lilly (Indianapolis, IN)
- …twins, computational modeling, edge/IoT, and analytics solutions. **Responsibilities:** The Associate Director - Digital Manufacturing Engineering position has ... streamlining processes, prioritizing work, and supporting the overall DME strategy. The Associate Director role will provide discipline leadership in technology… more
- Sanofi Group (Ridgefield, NJ)
- The Associate Director Quality is part of the Quality Assurance Department at Ridgefield, NJ. This role is responsible for providing direction and managing Teams ... objectives are to ensure product testing, release and continued process control and to: + Provides direct supervision to...Teams and cross-functional groups related to site operations The Associate Director Quality Compliance is expected to… more
