Quality assurance technician serp_jobs.h1.location_city
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Quality assurance technician • lincoln ne
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Associate provides quality assurance oversight for biological starting materials (Master Seed / Cell Banks) and raw materials for immunological and biopharmaceutical products used in the research and...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
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Zoetis is the world's largest Manufacturer and Supplier of Animal Pharmaceuticals.At Zoetis in Lincoln, NE, we manufacture high quality medicines for dogs, cats, and livestock.Our plant has been re...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
Zoetis is the world's largest Manufacturer and Supplier of Animal Pharmaceuticals.At Zoetis in Lincoln, NE, we manufacture high quality medicines for dogs, cats, and livestock.Our plant has been re...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_30
Quality System and employment of continuous improvement activities.This includes identifying or developing quality management tools assessing risks and leading root cause investigations evaluating ...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
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Monitors customer interactions and reviews and analyzes customer feedback to evaluate overall customer experience.Assigns root cause and identifies systemic quality problems.Assists with implementa...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
Any salary estimation specified in this job board may or may not be aligned with our organization's pay philosophy.Apply to connect with a Talent Acquisition Partner who can provide you more detail...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
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This position will be remote, but with a preference for candidates in Colorado, Texas, North Carolina, and Tennessee.This is your chance to be part of an in-house Brands team of industry experts in...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
General Dynamics Ordnance and Tactical Systems (OTS) is a global leader in the design, engineering and production of munitions, energetics, weapons, armaments, and missile subsystems around the wor...serp_jobs.internal_linking.show_moreserp_jobs.last_updated.last_updated_variable_days
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job_description.job_card.job_descriptionReview and approve SOPs, protocols, risk assessments and other process documents related to biological bank activities and material selection. Partner closely with Global and Site-based Manufacturing Quality Assurance to align with on-site operational requirements and best practices. Conduct internal compliance audits of MS / MC processes, ensuring alignment with internal procedures, quality standards and regulatory requirements. Investigate deviations, non-conformances, and implement effective CAPA associated with master seed / cell production and raw material selection. Support internal, external, and regulatory inspections acting as subject matter expert for MS / MC banks and associated raw materials. Utilize Global Quality Systems, as needed, including SAP, ETS and Veeva Vault. Work with R&D, MS / MC Manufacturing, Regulatory Affairs, and Supply Chain to ensure compliance during development and production of MS / MC banks. Provide QA guidance during development and scale-up of new MS / MC banks and processes. Participate in staff and project meetings, document reviews, and consultations with VMRD colleagues. Identify and support improvements in QA processes, documentation practices, and material selection. Monitor regulatory trends and update practices to maintain compliance. May assume a lead role for various QA projects within the PSQL group and / or VMRD. Support the identification, selection, and risk evaluation of raw materials and critical reagents used during research and development. Assist in developing specifications, risk assessments, and control strategies for raw materials, ensuring alignment with relevant regulatory expectations. Support review of supplier documentation, certificates of analysis, and change notifications. Bachelor's or Master's degree in Biology, Microbiology, Biotechnology, Chemistry, Animal Science, or related field. 3+ experience in Quality Assurance within the pharmaceutical, biotechnology, or animal health industry with Experience with product development, biological bank oversight, and / or raw material selection. Working knowledge of GMP, GLP, and relevant regulatory requirements (e.g., USDA, FDA, EMA). Experience utilizing enterprise systems (e.g., SAP, ETS, Veeva Vault) to support documentation, traceability, and process management activities is highly desirable. Experience with veterinary biologics or vaccines. Familiarity with cell culture, fermentation, or seed / cell bank processes. Experience leading QA projects or compliance initiatives. Demonstrated ability to work independently and in cross-functional teams. Ability to travel as needed (5-15%). Experience supporting regulatory submissions, inspections, or compliance activities is highly desirable. Strong documentation, organizational, and communication skills. Demonstrated proficiency for documentation review with a strong attention to detail.
The Product Development QA Sr. Associate provides quality assurance oversight for biological starting materials (Master Seed / Cell Banks) and raw materials for immunological and biopharmaceutical products used in the research and development of veterinary medicinal products. The role is compliance focused and is responsible for reviewing and approving documents related to raw material selection, production, and testing. Additional responsibilities include generating certificates of analysis and TSE / BSE compliance statements for both internal and external use. The Sr. Associate partners closely across R&D, Master Seed / Master Cell (MS / MC) Manufacturing, Supply Chain, and Regulatory Affairs teams, and is responsible for ensuring compliance with internal quality standards and regulatory guidelines, including those from the USDA Center for Veterinary Biologics (CVB), FDA Center for Veterinary Medicine (CVM), and EMA Committee for Medicinal Products for Veterinary Use (CVMP).
Key Responsibilities
Master Seed / Cell Bank Quality Oversight
- Oversee the establishment, characterization, and maintenance of MS / MC banks in compliance with internal and regulatory standards.
- Review and approve production records, testing records, stability reports, and requalification documentation to ensure accuracy, completeness, and compliance with regulatory and internal requirements.
- Ensure traceability and documentation of all Master Seed / Cell banks.
Quality Systems & Compliance
Cross-functional Collaboration
Continuous Improvement
Raw Material Support
Basic Qualifications
Preferred Qualifications
About Zoetis
At Zoetis , our purpose is to nurture the world and humankind by advancing care for animals. As a Fortune 500 company and the world leader in animal health, we discover, develop, manufacture and commercialize vaccines, medicines, diagnostics and other technologies for companion animals and livestock. We know our people drive our success. Our award-winning culture, built around our Core Beliefs, focuses on our colleagues' careers, connection and support. We offer competitive healthcare and retirement savings benefits, along with an array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources.
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