QC Supervisor
Listed on 2026-02-18
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Quality Assurance - QA/QC
Quality Control / Manager, QA Specialist / Manager, Quality Technician/ Inspector
We understand that the world we want tomorrow starts with how we do business today, and that’s why we’re inspired to make A Better World for Pets. Antech is comprised of a diverse team of individuals who are committed to each other’s growth and development. Our culture is centered on our guiding philosophy, The Five Principles:
Quality, Responsibility, Mutuality, Efficiency and Freedom. Today Antech is driving the future of pet health as part of Mars Science & Diagnostics, a family-owned company focused on veterinary care.
Current Associates will need to apply through the internal career site. Please log into Workday and click on Menu or View All Apps, select the Jobs Hub app, then click the magnifying glass to Browse Jobs.
The Target Pay Range for this position is $86,240.
- $107,800 annually. At Antech, pay decisions are determined using factors such as relevant job‑related skills, experience, education, training and budget.
The QC Supervisor is responsible for leading Quality Control immunoassay testing activities in a regulated biotech environment. This role oversees QC execution, data review, and team performance to ensure accurate, compliant, and timely release of materials and products. The QC Supervisor serves as a technical and people leader, supporting product lifecycle activities and maintaining high standards of data integrity and quality.
EssentialDuties And Responsibilities
- Supervise daily QC laboratory operations and related bioanalytical methods
- Ensure assays are performed in compliance with SOPs, ISO 9001, and regulatory requirements
- Review and approve QC data, calculations, trends, and reports for accuracy and compliance
- Lead and support investigations related to OOS/OOT results, product variability, and system suitability failures
- Provide technical guidance on assay troubleshooting, optimization, and robustness
- Manage training and qualification of QC analysts on SOPs.
- Support product validation, transfer, and lifecycle management of veterinary diagnostic products.
- Oversee reagent qualification, critical material management, and reference standard control
- Ensure laboratory equipment is qualified, calibrated, and maintained
- Partner with Quality, Manufacturing, and Process Development to resolve quality and assay‑related issues
- Support internal, client, and regulatory audits and inspections
- Drive continuous improvement initiatives related to assay performance, throughput, and compliance
- Bachelor’s degree (with 5 years industry experience) or Master’s degree (with 2 years of industry experience) in Biochemistry, Chemistry, Immunology, Bioanalytical Science, or a related field.
- 1‑2 years of supervisory or technical lead experience.
- Experience supporting regulatory inspections involving bioanalytical or immunoassay methods
- Experience in CLSI guidelines on assay validation (Accuracy, precision, sensitivity, specificity, robustness)
- Exposure to automation or high‑throughput immunoassay platforms (preferred).
Skills And Abilities
- Hands‑on experience with biotechnology processes and principles.
- Strong written and oral communication skills, including technical reporting.
- Knowledge of statistical analysis methods.
- Ability to handle and document sensitive and confidential information appropriately.
- Strong understanding of laboratory safety, documentation practices, and operational requirements.
The associate is regularly required to apply manual dexterity, including hand/wrist flexibility, for computer keyboarding. The associate frequently is required to sit for extended periods of time, stand, walk, and reach with hands and arms. The associate is frequently required to hear and speak in order to use the telephone, make presentations and communicate with people in an office environment. The associate is occasionally required to sit and stoop, bend, kneel, or crouch.
Work will be performed in an office, laboratory, and process assembly/manufacturing environment. Able to use standard office equipment (computer, phone), know and understand laboratory safety protocols, and operate in an around process assembly equipment. Able to walk, stand,…
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