- Otsuka America Pharmaceutical Inc. (Richmond, VA)
- Job Summary The Associate Director , Global Product Quality - GMP Process is responsible for enabling the optimization and harmonization of key GMP ... coaching, and subject matter expertise to global teams on GMP compliance and quality system execution. Qualifications...to global teams on GMP compliance and quality system execution. Qualifications Required Bachelor's degree in Pharmacy,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of Quality Management System (QMS) establishment processes in collaboration with GMP Quality System function. Supports the development and implementation of ... Ensure effective collaboration with DS affiliates to promote a culture of quality that drives performance and teamwork.Responsibilities: GMP Audit: Support the… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Quality Associate Director / GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, encompassing ... and Skills: Minimum of five (5) years of manufacturing, technology, laboratory, and/or quality operations experience within GMP environment GMP Compliance… more
- Otsuka America Pharmaceutical Inc. (St. Paul, MN)
- Job Summary The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products ... studies as well as drive continuous improvement. Job Description Responsible for directing quality oversight of GMP contract manufacturers of Otsuka clinical and… more
- Merck & Co. (Rahway, NJ)
- …into the Director , Logistics and Distribution Technology the Associate Director , Logistics and Distribution Technology will be responsible ... skills to shape the technical capabilities lead a global, cross-modality technical team.The Associate Director will lead a team of technical experts responsible… more
- Lilly (Pleasant Prairie, WI)
- …on new manufacturing investments and new state of the art QC laboratories. The Associate Director , Quality Control (QC) - Chemistry, is responsible for ... in a scientific field (preferably chemistry) Minimum of 5 years' GMP Quality Control Laboratory experience including instrument qualification, analytical… more
- Lilly (Pleasant Prairie, WI)
- …driving solutions that impact the site and align with corporate objectives. The Associate Director , Quality Assurance, will also provide computer system ... production. This role will leverage a deep understanding of GMP data flows (electronic and paper), the application of...impact the site and align with corporate objectives. The Associate Director , Quality Assurance, will… 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
- Bristol Myers Squibb (Madison, NJ)
- …and collaborate extensively with teams and leaders across the BMS network. The Associate Director will support BMS' GMP /GDP Inspection Readiness strategy ... personal lives. Read more: careers.bms.com/working-with-us . Position Summary Reporting to the Director , Inspection Readiness, the Associate Director will… more
- Lilly (Lebanon, IN)
- …to enable a successful startup into GMP manufacturing operations. Overview: The Associate Director - Operational Readiness is a key site leader responsible ... activities are delivered safely, on time, and to the required quality standards. Responsibilities: Strategic Planning: Drive operational readiness strategies to… more
- Lilly (Indianapolis, IN)
- …lead the charge in shaping the future of manufacturing at Eli Lilly? As an Associate Director of Engineering, you'll be at the forefront of this exciting ... of leaders, you'll influence and implement our organizational agenda, business priorities, and quality objectives to drive success down to the floor level. Join us… more
- AbbVie (North Chicago, IL)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible ... is to use their broad understanding of Product Development, Manufacturing, Quality and Regulatory Affairs to translate the business objectives into actionable… more
- Parexel (Salt Lake City, UT)
- …associated with audits and regulatory inspections in liaison with LSAD and Clinical Quality Associate Director (CQAD). Ensures timely collection/uploading of ... other CRAs and the Local Study Team/ Local Study Associate Director (LSAD) to ensure that study...site staff in study related matters, including Risk Based Quality Management (RbQM) principles. Confirms that site staff have… more
- Bristol Myers Squibb (Summit, NJ)
- …Improvement within the Manufacturing Operations function. This position reports to Associate Director , Manufacturing. Shift Available: Monday - Friday, Onsite ... to the BMS values of Inclusion, Accountability, Innovation, Urgency and Passion. GMP Is accountable to ensure their Manufacturing Managers and their WCT members… more
- Merck (Rahway, NJ)
- …Reporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform Packaging ... compliant supply of commercialized products for the benefit of patients. The Associate Director of MDCP Platform Packaging and Assembly Technical Leadership… more
- Sysco (St. Charles, MO)
- …Safety Program (Food Safety Program Manager) reports directly to a GSC Field Director , Food Safety and has dotted line reporting to the OpSite Regional President. ... for audit non-conformance(s). Reviews results with Field Food Safety Director . Acts as the site's primary contact during Food...School or GED Equivalent Required. In lieu of an associate or bachelor's Degree, a combination of education and… more
- Otsuka America Pharmaceutical Inc. (Little Rock, AR)
- **Job Summary** The Associate Director , Global Product Quality - GMP Process is responsible for enabling the optimization and harmonization of key GMP ... coaching, and subject matter expertise to global teams on GMP compliance and quality system execution. **Qualifications**...to global teams on GMP compliance and quality system execution. **Qualifications** Required + Bachelor's degree in… more
- Compass Group, North America (Wilmington, MA)
- ESFM **Position Title: GMP UNIT DIRECTOR ** **Salary: $90,000 - $100,000** **Other Forms of Compensation:** None ESFM is the corporate facilities management (FM) ... FAQs and the Compass Employee Referral Policy, email MyReferral@compass-usa.com._** **Job Summary** The ** GMP Unit Director ** will be the on-site leader for our… more
- Merck (Durham, NC)
- **Job Description** The Quality Associate Director / GMP Lead Site Auditor will have leadership responsibility for the site internal audit program, ... Skills:** + Minimum of five (5) years of manufacturing, technology, laboratory, and/or quality operations experience within GMP environment + GMP Compliance… more
- Catalent Pharma Solutions (Philadelphia, PA)
- ** Associate Director , Quality Assurance** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) ... **This is a full-time salaried position, onsite out of Philadelphia, PA.** The ** Associate Director , Quality Assurance** is responsible for providing… more
