- Merck & Co. (Rahway, NJ)
- …a high degree of technical and project management responsibility. The Specialist -Engineering position will report to the Associate Director, Engineering and ... scaling up new chemistries, and exploring new technologies. - Responsibilities of the Specialist - Engineer include the following: The engineer role at the … more
- Merck & Co. (Rahway, NJ)
- …production, utility systems and associated infrastructure.- Responsibilities of the Specialist -Process Supervisor include the following:The process supervisor role ... at the Specialist level will serve as an operations team member...Supervisor will assist on daily production activities while ensuring compliance with Safety, GMP, and Environmental requirements to meet… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Metrology Specialist as part of the Technical Operations team based in Raritan, NJ. ... position will be responsible for metrology support for cGMP Clinical and Commercial Cell Therapy Manufacturing. This individual will partner with various Technical… more
- 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 ... is part of Our Company Research Laboratories (RL).The Senior Specialist , Global Professional Engagement serves as a key professional...18 months of experience in US and ex-US Regulatory, Compliance and Risk Management aspects and ability to lead… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …Contracts Specialist will provide end-to-end execution of Federal and commercial contracts by ensuring compliance with Institute policies, Federal ... Contracts Specialist must have demonstrated experience working in a commercial or Federal contracting environment and a fundamental understanding of standard… more
- Merck & Co. (Durham, NC)
- …intermediates and finished products. We have an exciting opportunity for a Senior Specialist to join the operations team for a capital project start-up in Durham, ... customers, above site partners, vendors) to support these initiatives. The Senior Specialist must be able to work efficiently in a fast-paced environment and… more
- Eisai, Inc (Sacramento, CA)
- …to work cross-functionally while adhering to all of Eisai's ethics and compliance standards. Senior Neurology Account Specialist (Sr NAS) Responsibilities ... impairment due to Alzheimer's disease (AD) or mild AD. TheSenior Neurology Account Specialist (Sr NAS) will be part of a diverse team of sales professionals… 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...production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environment. This… 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...CAR-T Equipment team in support of on-going clinical and commercial manufacturing as well as facility expansions and improvements.Key… 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 ... for maintenance support and mechanical system operations for cGMP Clinical and Commercial Cell Therapy Manufacturing on a modified second shift. This individual will… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking QA Document Control Specialist as part of the Quality team based in Raritan, NJ. Role OverviewThe ... Quality Assurance Document Control Specialist role is an exempt position responsible for supporting...cell therapy manufacturing facility to support both clinical and commercial requirements in a sterile GMP environment. This role… more
- Merck & Co. (Durham, NC)
- Job DescriptionThe Specialist is a member of the Focus Factory Automation team responsible for the assigned process control systems in support of manufacturing ... of process control, data collection techniques, and troubleshooting in compliance with SDLC, GMP, safety, and environmental regulations.- Actively support,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking Change Control Specialist as part of the Technical Operations team based in Raritan. Role ... OverviewThe Change Control Specialist will be part of the Technical Operations team...production of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP cleanroom environmentKey Responsibilities… 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...manufacturing of autologous CAR-T products for clinical trials and commercial operation in a controlled cGMP environment. Reviews, inspection,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Provides continuous training on contract management process and technology to ensure compliance by all Commercial employees, including new hires. Assists in ... overseeing the day-to-day operation of contract management procedure for the Commercial and Development divisions; (B) Providing employee training on the contract… more
- Merck & Co. (Durham, NC)
- …This position is accountable for performing lot release testing in compliance with standard operating procedures, safety, and cGMP regulations. Primary duties ... capture forms, equipment logbooks, and inventory formsEnter data evaluated for compliance to specifications and report abnormalities.Maintain lab areas and equipment… more
- Merck & Co. (Rahway, NJ)
- …progress of growth.Familiarity with US and EU GMP and Safety compliance regulations.Desire and willingness to learn, contribute and lead through independent ... Knowledge of Investigational drug regulatory requirementsAudit experience: safety, environmental, compliance /qualityUnderstanding of Clinical Supply Chain OperationsExperience with Commissioning, Qualification… more
- Merck & Co. (Austin, TX)
- Job Description RESPONSIBILITIES: Provide special Mobile Apps compliance and SOP Audit input and compliance reviews.Engage Markets and requestors on Mobile Apps ... related to mobile listings, Apps feedback and compliance .Manage vulnerability and technical scanning of mobility applications and ensure applications meet required… more
- Merck & Co. (Durham, NC)
- …and protocolsComplies with policies and procedures in order to maintain compliance with legal.regulations, health and safety, and regulatory requirements as ... determines require routine collaboration with external stakeholders, such as customer-facing commercial , or research-based roles, will be expected to comply not only… more
- Merck & Co. (Rahway, NJ)
- …models and deliver solutions with high quality standards, timeliness, compliance and excellent user experience.Contribute to innovative experiments, specifically to ... determines require routine collaboration with external stakeholders, such as customer-facing commercial , or research-based roles, will be expected to comply not only… more
