- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of ... the Technical Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide… more
- Merck & Co. (North Wales, PA)
- …development and implementation of global publication strategies and tactical plans. The Associate Director Pub Manager oversees compliance with our company's ... Job DescriptionOverview:The Associate Director Publication (Pub) Manager is the central...Policies and ProceduresProvide regular and ad hoc publication process compliance training to Publication TeamsConduct business in accordance with… 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 ... variety of activities pertaining to supporting, maintaining, and assuring compliance with quality systems requirements and applicable regulatory requirements; to… more
- Merck & Co. (North Wales, PA)
- …to discover the next medical breakthrough.Position Description: The Associate Principal Scientist Statistical Programming leads the statistical programming ... areas of focus include:the assurance of deliverable quality and process compliance ,effective deliverable development utilizing global and TA standards that optimize… 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 ... manufacturing areas. Under general supervision, the role provides support and compliance oversight to Manufacturing and Facilities and Engineering staff in the… more
- 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 ... at our company's Millsboro Animal Health facilities. This role is highly compliance -driven in accordance with State and Federal regulations as applicable to the… more
- Catalent (San Diego, CA)
- Quality Assurance Associate , Clinical SuppliesPosition Summary: Catalent Pharma in San Diego, CA is hiring a Quality Assurance (QA) Associate , Clinical Supplies ... . Under general supervision, the QA Associate performs work that is varied and that may...a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer,… more
- Merck & Co. (North Wales, PA)
- …Hybrid work model (combination of in-office and work from home abilities).The- Associate Director, Digital & Omnichannel Innovation for US Oncology-focuses on digital ... teams in order to build partnerships and trust with Commercial Legal, Compliance , Privacy and Regulatory colleagues to effectively alleviate concerns and mitigate… more
- Merck & Co. (Durham, NC)
- …- 6:30 AM rotation (2-2-3). -The VMF (Vaccine Manufacturing Facility) Associate Production Technician is an excellent entry-level opportunity for recent university ... through hands on processing activities. Key responsibilities for the Associate Production Technician include the execution of aseptic processing requirements,… more
- Novo Nordisk Inc. (Atlanta, GA)
- …rights and wellbeing; data reliability; scientific integrity; regulatory and process compliance ) for monitoring and site management activities. Takes ownership to ... deliver upon near-term North America Clinical Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex improvement/innovation projects for the department, (subset of)… 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...GMPs. This individual will be responsible for evaluating the compliance of documents such as batch records, equipment records,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Associate Director, Marketing Operations Procurement (Hybrid) Working as part of a global & dynamic team, this position is ... both Patient Access, CSO, and Market Access.Supplier Relationship Management (SRM):Support Associate Director and SSC on improving Service Delivery via Enhanced… 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)
- …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 ... Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance Performing and monitoring critical processes with the ability to perform basic… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Field Access, and Payer), Brand Marketing, Training, Market Access, Trade, Legal, Compliance , Finance, HEOR, and Market Research. The position has high exposure to ... market access, commercial insights and analytics, sales, medical/CMR, legal, compliance , and regulatory. Other internal relationships include Public Affairs,… more
- Merck & Co. (Rahway, NJ)
- …environmental impact and advancing sustainability across its global operations. The Associate Director, renewable energy and carbon offset procurement lead will be ... are grouped into center-led categories and regional operating teams.Position Description:The Associate Director of Renewable Energy and Carbon Offset Procurement and… more
- Aequor (Devers, TX)
- …Mon)This role is 100% OnsiteSome OT required as neededJob Description: Bio-Process Associate 1st shiftThis role is in Devens, MA100% OnsitePlease refer to attached ... in a timely manner. Follows detailed SOP's and batch records. Ensures compliance with cGMP and safety requirements. Maintains files, records and equipment. Records… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …make the appropriate changes to ensure trial conduct is completed in compliance and meets Novo Nordisk's business standards Risk management: Assessing and mitigating ... milestones and related payment schedules) Advanced knowledge of regulatory and compliance requirements for clinical research, ICH GCP Principles and the application… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …and Preventive Actions (CAPA) process, and is responsible for ensuring compliance within quality systems processes. Key Responsibilities Lead the CAPA program ... continuous improvement of quality systems processes. Implement processes to ensure compliance with current Good Manufacturing Practices (cGMP). Manage multiple and… more
- Aequor (Thousand Oaks, CA)
- …degree and 2 years of experience OR Bachelor's degree and 4 years of experience OR Associate 's degree and 8 years of experience OR High school diploma / GED and 10 ... Some database/reporting experience, programming languages, application support, data migration and such. While this is not a purely technical role per say, those skills will be valuable/necessary for some of the other aspects of the work we have beyond process… more
