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The Specialist, QA Engineering is responsible for ensuring quality, integrity, and compliance of site Information Technology (IT) systems, review of validation and qualification documents for all equipment and facility activities.
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The Desktop Support Specialist provides a higher level of technical support through analysis and problem solving to facilitate installation, implementation, maintenance, education, and documentation of a variety of computer and software technologies.
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In support of this model, roles have been categorized into one of four work location categories: onsite roles, hybrid roles that are a blend of onsite and remote work, remote local roles that are primarily home-based but require some level of purpose-driven in-person interaction and living within a commutable distance, and remote non-local roles that can be effectively performed remotely with the ability to work in approved states.
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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. A background of pharmaceutical manufacturing or quality control/quality assurance is a plus.
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Manufacturing quality technician. Employee is responsible to follow and uphold all Food Safety, Food Quality, Occupational Safety, Health and Environment policies and procedures as pertains to role.
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3-5 years of experience in drug safety, pharmacovigilance, quality assurance, or a related field. Provide drug safety and pharmacovigilance leadership to the quality and compliance team, fostering a culture of collaboration, excellence, and continuous learning.
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Posting Summary Rutgers, The State University of New Jersey, is seeking a Program Development Analyst – Quality Improvement, Assessment, and Accreditation Specialist for the Office of Education at the Robert Wood Johnson Medical School.
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The Specialist, QA Engineering is responsible for ensuring quality, integrity, and compliance of site Information Technology (IT) systems, and review of validation and qualification documents for all equipment and facility activities.
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National Certified Peer Recovery Support Specialist (NCPRSS) and/or Certified Peer Recovery Specialist (CPRS). The Peer Recovery Specialist assists in the provision of Behavioral Health Services to clients and families.
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Job Summary: The Edibles, Production Specialist provides on-site support to the production areas within a cannabis cultivation facility. As a Production Specialist, you are responsible for supporting the manufacturing of cannabis infused edibles and assembling and packaging products for distribution.
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Job Summary:Develop, implement and maintain programs and processes that will ensure a safe and environmentally responsible work environment and compliance with applicable regulatory requirements/company procedures, minimize EHS related risk to Labcorp, and strive for EHS excellence.
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Mountain RAM) and quality systems software (e.g. Veeva). Must have knowledge and experience with GMP, Quality and compliance. Intermediate knowledge of quality systems including CAPA, change control, and document management systems.
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Title: Specialist, QA Engineering. Previous experience as a computer system validation / quality assurance for life sciences company regulated by. Support any other goals and objectives of the site Quality Assurance organization, as needed.
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Position OverviewAs an Operations Specialist in Animal Care, your role will be to ensure that proper animal care and husbandry is being provided for all companion animals and aquatic life in the Pet Care Center (PCC.
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Experience with Veeva (Quality Docs, QMS and Training modules) a plus. Global Pharmaceutical company, with US HQ in Central New Jersey, focused in Metabolics, Endocrinology and Oncology is expandingLooking for a strong Quality Assurance Manager for the entire North American manufacturing and quality organization.
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Title: quality specialist Company: Direct Line Global in Bridgewater, NJ
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