- Merck & Co. (North Wales, PA)
- Job DescriptionRole Summary The Senior Specialist Global Professional Engagement is a member of the GEMS Consulting & Medical Education team within, V&I Global ... (GMSA), which is part of Our Company Research Laboratories (RL).The Senior Specialist , Global Professional Engagement serves as a key professional interface with… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …treatment of multiple myeloma.Legend Biotech is seeking a Master Data Governance Sr. Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... OverviewWe are actively seeking a proficient Master Data Governance Sr. Specialist with a specific focus on Materials orchestration throughout the End-to-End… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …The Position This position will review manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... assess Corrective and Preventive Actions Reviews and approves validation documentation Reviews and assesses deviations; includes tracking, follow-up and… more
- Merck & Co. (Durham, NC)
- …our incredibly high standards of quality and meets all regulatory requirements. Partnering across our internal manufacturing facilities, externalcontract ... order to maintain compliance with legal.regulations, health and safety, and regulatory requirements as written.Works in a team environment to accomplish departmental… more
- Merck & Co. (Durham, NC)
- …with our incredibly high standards of quality and meets all regulatory requirements.- Partnering across our internal manufacturing facilities, external contract ... lab operations.- Responsibilities Support routine release testing Complete appropriate documentation supporting testing procedures, including data capture forms, equipment… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Merck & Co. (Rahway, NJ)
- …supplies to augment and accelerate our products.Author and review GxP documentation including but not limited to batch records, specification, equipment ... manufacturing in pilot plant environment.Experience reviewing and approving GxP documentation , quality investigations and change management.Extensive knowledge and experience… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …contact for matters concerning contracts. Maintain records for correspondence and documentation in relation to established contracts and those in progress. ... charts, team lists and track projectsProvide Strategy Operations support for regulatory inspection related activities as required such as ensuring logistics for… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Maintenance Specialist as part of the Technical Operations team based in Raritan, New ... status in at leastoneReads and interprets blueprints, P&IDs, and drawingsUtilize good documentation practices (GDP) for all work performed on the CMMS system… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Operations Inventory Control Specialist as part of the Technical Operations team based in Raritan, New ... Jersey. Role OverviewThe Operations Inventory Control Specialist will be part of the Raritan CAR-T Operations team responsible for building operations activity area… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Warehouse Specialist as part of the Technical Operations team based in Raritan. Role ... OverviewThe Warehouse Specialist will be part of the Technical Operations team...within the electronic inventory management system.Prepares, reviews and maintains documentation , runs reports, metrics, coordinates and schedules with internal… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of multiple myeloma.Legend Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe ... QA Warehouse Incoming/Raw Material Specialist is an exempt level position with responsibility to...and record results to complete receipt process. Reviews inspection documentation (C of A or other Material Certifications) for… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist as part of the Quality Operations team based in Raritan, New Jersey. Role ... OverviewThe QA Shop Floor Specialist is an exempt level position responsible for the...path forward for manufacturing issues.Real time review of all documentation , and reporting, in support of process unit operations,… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... signature authority for deviation closure Reviews and approves Validation Documentation Reviews and assesses Corrective and Preventive Action Reports Participates… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a Technical Equipment Specialist as part of the Technical Operations team based in Raritan, NJ. Role ... OverviewThe Technical Equipment Specialist will be responsible for ensuring equipment/systems required to support an expanding Cell Therapy facility is appropriately… more
- LSI Solutions (Victor, NY)
- …state-of-the-art devices. After all, our customer is ultimately the patient. JOB TITLE: Regulatory Specialist (Labeling) - Days 8:00AM to 5:00PM SALARY RANGE: ... LOCATION: Onsite at LSI Solutions in Victor, NY JOB SUMMARY: The Regulatory Specialist applies her/his experience, knowledge, organization skills, and… more
- Guthrie (Sayre, PA)
- …DESCRIPTION: Under the direction of the VP, Pharmacy Services, the Pharmacy Clinical Specialist - Regulatory Compliance is responsible for ensuring the delivery ... development, coordination, implementation, and evaluation of Compliance issues related to regulatory or practice standards. The Pharmacy Compliance Specialist … more
- University of Pennsylvania (Philadelphia, PA)
- …maintain all regulatory affairs documentation /files as required. The Regulatory Affairs Start-Up Specialist -CC is expected to resolve, with minimal ... wellness programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile Title Clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …Title Regulatory Affairs Specialist C Job Profile Title Clinical Research Regulatory Specialist C Job Description Summary The Regulatory Affairs ... C functions independently with minimal supervision on complex protocols. The Regulatory Affairs Specialist C reviews and creates core documents (protocols,… more
- University of Pennsylvania (Philadelphia, PA)
- …Clinical Research Regulatory Specialist will prepare and process all regulatory documentation through the IRB, CTSRMC, etc., and all applicable ... resources, and much more. Posted Job Title Clinical Research Regulatory Specialist A (Department of Otorhinolaryngology) Job...affairs documentation /files as needed. The Clinical Research Regulatory Specialist is expected to resolve … more
