- Merck & Co. (Millsboro, DE)
- …Delaware seeks to add an Attending Veterinarian in the role of Associate Director.This position will have overall responsibility for oversight and administration of ... training and oversight of the animal care staff, serving as a designated reviewer and voting member of the Institutional Animal Care and Use Committee (IACUC),… more
- Merck & Co. (North Wales, PA)
- …to the Director/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review ... objectives.Serve as the liaison and manages correspondence with FDA's promotional review divisions Office of Promotion and Advertising Review (OPDP)/Advertising… more
- Software Galaxy Systems, LLC (Plaquemine, LA)
- …and attention to details. SAP experience is preferable. Responsibilities: Review Production Batch Records and other manufacturing-related documents to verify ... products to ensure compliance with established specifications and regulatory standards. Review , revise, and create SOPs as needed. Assist in the implementation… more
- Catalent (San Diego, CA)
- Quality Assurance Associate II - Manufacturing Catalent Pharma Solutions in San Diego is currently hiring a Manufacturing Quality Assurance (MQA) Associate II ... the development and manufacture of drug candidates. This will include documentation review and approval, dispositioning of product or its intermediates & supporting… more
- Catalent (San Diego, CA)
- Job Title: Quality Assurance Associate , Analytical City: San Diego State : CA JOB DESCRIPTION: Review of analytical release and stability data, involving ... (PXRD), Thermogravimetric analyzer (TGA) and Differential Scanning Calorimeter (DSC). Review Hardness testing and Friability of tablets, Content Uniformity and… more
- Catalent (San Diego, CA)
- Quality Assurance Associate I, ManufacturingCatalent Pharma Solutions in San Diego is currently hiring a Quality Assurance Associate I in our QA Manufacturing ... group. A QA Associate I must be familiar with applicable GMPs. This...regulations.Liaison between Manufacturing and QA for executed Batch Record Review and flow of documents.Liaison between QA and client… more
- Merck & Co. (North Wales, PA)
- Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central source of information regarding publication activities and is responsible for ... and implementation of global publication strategies and tactical plans. The Associate Director Pub Manager oversees compliance with our company's publication… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …is responsible for the overall quality of materials subject to Product Material Review Process (PMRP) - including but not limited to: Brand sales materials, Training ... the brand teams as well as the Product Material Review Team (PMRT) with the Legal, and Medical Affairs...needed for PMRP and assist with the scheduling and review of PMRP for Global submissions. This individual will… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …that fall under the responsibility of the R&D Procurement group. The Associate coordinates with R&D Procurement team members, Purchasing, Legal, Finance, vendors and ... needed.Responsibilities- Contract Coordination: Collate exhibits to create contract draft, Review contract documents for completeness and accuracy; Ensure compliant… more
- Eisai, Inc (NJ)
- …this is your profile, we want to hear from you. Job Summary The Associate Director, Clinical Outsourcing, will oversee and lead and support activities related to the ... and managing service provider business relationships in alignment with global strategies. Review and approve Clinical Quality Assurance audit plans and reports.… more
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Associate Specialist - Manufacturing Automation position will report to the Director, ... production, utility systems and associated infrastructure.- Responsibilities of the Associate Specialist - Manufacturing Automation include the following: Small… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director, Global Vaccines Communications for the company's pneumococcal and pediatrics franchise will collaborate closely with ... programs in support of the US and global vaccines businesses.-The Associate Director will report to the Director, Global Vaccines Communications.Primary… more
- Aequor (Seattle, WA)
- …working cross-functionally Position Summary: The Quality Assurance Document Control (QADC) Associate Specialist supports the cGMP Document Control operations for the ... including the document approvals, document change control process, periodic review and system reporting. Duties/Responsibilities: Primary responsibilities include: Managing… more
- Aequor (Thousand Oaks, CA)
- …if going well ** Must be within 1hour away or 30/50 miles MCS Mfg Associate MCS Manufacturing Associate -EW Job DescriptionJob Summary The Associate of ... and implementing improvements related to routine functions Assisting in the review of documentation for assigned functions (equipment logs, batch records) Performing… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …of research and strategic partnership contracting agreements. In collaboration with the Associate Director, the Associate Manager will support CMR's partnership ... internal and external stakeholders Relationships This position reports to an Associate Director overseeing the contract management function of the CMR organization.… more
- Aequor (Thousand Oaks, CA)
- …floor. Detail Oriented, Team player and Quality Experience. The Sr. Associate Quality Assurance position supports 's Quality Assurance program under the ... floor, inc. Inspection support, ASP and QA assessments, Electronic batch record review , SOP revision approval, Maximo System - Work order, job plan approvals,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical ... post trial information on required public forums (eg.clinicaltrials.gov).- Under supervision, review and document CRO-generated reports, such as site monitoring trip… more
- Eisai, Inc (Nutley, NJ)
- …to hear from you.JOB SUMMARY:As a member of the Data Analytics group, the Associate Director, Commercial Analytics is part of a high performing team that provides ... identify solutions to field needs with existing report data. Lead the review of recommended solutions with field leadership for confirmation and development of… more
- Merck & Co. (Boston, MA)
- Job DescriptionThe Associate Vice President (AVP)/Therapeutic Area Head, Immunology Translational Medicine, will be responsible for leading the Translational ... TMed at governance for the Immunology portfolio (discovery therapeutic area review , early and late-stage clinical governance), and fully supportive of external-based… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director, Global Marketing will join the New Assets Brand Strategy team and help build the future of our Company's Oncology. This role ... Process (specifically in launch stage). Experience with end-to-end medical/legal review and delivery processes. Previous experience at operating company level… more
