• Legend Biotech USA, Inc. (Raritan, NJ)
    …position with responsibilities for providing quality oversight over the validation and qualification activities for equipment, systems, computer systems, and ... validation , shipping validation , and data integrity.Key Responsibilities Provide quality and compliance oversight for computer systems validation ,… more
    HireLifeScience (07/02/25)
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  • Merck & Co. (Rahway, NJ)
    Validation Specialist will work as part of the integrated US Metrology and Validation team and drive a culture of quality and operational excellence across ... and instrumentation in both GMP and non-GMP environment Participate in laboratory computer system validation activities associated with new or upgraded… more
    HireLifeScience (07/26/25)
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  • Merck & Co. (Rahway, NJ)
    …approve GMP procedures and documentation, with an emphasis on Qualification and Validation plans around equipment, critical utilities, and computer systems.- ... and Original Equipment Manufacturers (OEM) and vendors.Provide engineering and quality engineering (QE) support, ensuring facility, utilities and equipment are… more
    HireLifeScience (07/26/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Services Lead plays a key role in overseeing the development, validation , implementation, and integration of GxP-regulated systems across the organization. This ... position ensures that all global systems, electronic records, validation processes, and regulated applications meet strict regulatory requirements, industry best… more
    HireLifeScience (05/30/25)
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  • Aequor (Cincinnati, OH)
    Quality Control Analyst I Does the position allow for the worker to be virtual/remote? No Temp to Perm: Temp to perm based on openings and performance Shift ... Perform routine and non-routine physical and chemical testing of commercial, validation and stability samples in accordance to written methodology Analyze data… more
    HireLifeScience (07/12/25)
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  • Eisai, Inc (Nutley, NJ)
    …analytical skills and report writing skills Experience with GxP systems including computer system validation and associated regulations, recommended. Ability to ... If this is your profile, we want to hear from you. Director, Clinical Quality Assurance The Director, Clinical Quality Assurance position is responsible for… more
    HireLifeScience (06/06/25)
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  • Twist BioScience (South San Francisco, CA)
    …Annex 11, and internal quality standards. Oversee and execute comprehensive computer system validation (CSV) activities, including IQ, OQ, PQ protocols and ... analytics, and data visualization capabilities to support operational decision-making and quality reviews.Compliance & Validation : Ensure our custom MES… more
    HireLifeScience (06/13/25)
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  • BioAgilytix (San Diego, CA)
    …specification, IQ/OQ/PQ, etc.) Contributes to the development and revision of Computer System Validation procedures and policies (validations, change control, ... with computer systems validationMinimum Preferred Qualifications: SkillsProficiency in Computer System Validation , following GxP regulations and GAMP… more
    HireLifeScience (07/03/25)
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  • BioAgilytix (Durham, NC)
    …That means hands-on work designing Azure Data Factory and API integrations, automating data- quality checks, and setting up clear governance so everyone knows who can ... keep BioAgilytix ahead of regulatory requirements.Key ResponsibilitiesData Governance & Quality Standards:Develop a foundational data governance framework, with hands-on… more
    HireLifeScience (07/01/25)
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  • Merck & Co. (Durham, NC)
    …make our products. We work in the manufacturing plants with a "Safety First, Quality Always" mindset striving for continuous improvement. We work in the local plant ... connected to our global manufacturing network to ensure the highest quality of raw materials, intermediates and finished products.-Position Description-This is a… more
    HireLifeScience (07/25/25)
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  • Merck & Co. (North Wales, PA)
    …that project plans are executed efficiently with timely and high quality deliverables.For assigned projects the position serves as the statistical programming ... lifecycle. Primary Activities :Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs… more
    HireLifeScience (07/26/25)
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  • Quality Chemical Laboratories (Wilmington, NC)
    …candidates for qualified analytical data reviewers, LabWare LIMS development/configuration/ validation , Document Control Associates, Computer System ... Quality Chemical Laboratories (QCL), a pharmaceutical testing and...in Chemistry or related science and experience in method development/ validation . Special consideration also given to experienced GMP data… more
    Upward (07/01/25)
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  • Aequor (Hicksville, OH)
    …paperwork for upcoming batches. Sets up and monitors cleaning and filling Validation batches according to protocols. Accepts and controls labels for individual ... feedback on operator performance. Interacts with production management, mechanics, and Quality Assurance. Participates in training of new employees. Adheres to all… more
    HireLifeScience (07/19/25)
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  • Legend Biotech USA, Inc. (Raritan, NJ)
    …training program for Operations (Manufacturing, Warehouse, Facilities & Engineering, Validation , Technical Support, Supply Chain) that supports daily clinical ... Training systemsKnowledge of LMS systemSupports the maintenance and reporting of quality training metricsJob duties performed routinely require exposure to and… more
    HireLifeScience (07/16/25)
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  • Merck & Co. (North Wales, PA)
    …in ensuring that project plans are executed efficiently with timely and high quality deliverables. - For assigned projects the position serves as the statistical ... - Primary Activities : Effective analysis and report programming development and validation utilizing global and TA standards and following departmental SOPs and… more
    HireLifeScience (05/21/25)
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  • Merck & Co. (Rahway, NJ)
    …for statistical programming deliverables. Contribute to the development and validation of datasets following CDISC standards. Generate tables, listings, and ... files and program text files for regulatory submission. Assure high quality and timely deliverables. Communicate and collaborate effectively with project team… more
    HireLifeScience (06/18/25)
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  • Merck & Co. (Rahway, NJ)
    …submission deliverables under the guidance of a senior level programmer.Perform validation tasks according to departmental SOPs and collaborate effectively with ... transport files and associated documentation for regulatory submissions.Assure deliverable quality and compliance with departmental SOPs and good programming… more
    HireLifeScience (06/17/25)
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  • Barry-Wehmiller Companies (Los Angeles, CA)
    …experience highly preferred 10+ years' experience with increasing responsibility in validation / quality service and project management of life sciences, biotech ... management tools and word processing skills. Working knowledge of process automation and computer system validation concepts, GAMP methodologies, 21 CFR Part 11… more
    Upward (07/05/25)
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  • Grand River Aseptic Manufacturing (Grand Rapids, MI)
    …knowledge of pharmaceutical manufacturing with GMPs, change control, risk management and quality by design. Must have proficient computer skills in project ... Quality , Service, Collaboration, Courage. Do you exhibit these...every day. Overview of this Position: The Sterility Assurance Validation Project Manager manages aseptic process simulation studies performed… more
    Upward (07/24/25)
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  • Sierra Nevada Corporation (Lone Tree, CO)
    As Director Engineering over the Test & Validation team, you will be using your skills and expertise to support the execution of IAS's engineering strategy, provide ... all phases of the integrated digital development process focused on verification/ validation . This includes the early phases of business development, through design… more
    Upward (07/28/25)
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