22 qc supervisor jobs found

Medline Industries, LP seeks a qualified QC Supervisor to oversee the Quality Control functions at a designated distribution center. You will manage performance, attendance, and reviews for direct reports and coordinate with Branch Management. Responsibilities include training inspectors on QSR/FDA regulations, ensuring regulatory compliance, and guiding day‑to‑day activities. Ability to lift up to 50 pounds and travel state-to-state may be required. #J-18808-Ljbffr

Nuclein, LLC is seeking a Quality Control Supervisor in the Austin, TX area to lead QC personnel, train staff, and ensure testing and inspection meet stringent quality standards for diagnostic devices and components. The role emphasizes applying rigorous QC methods, maintaining GMP standards, and driving continuous improvement while collaborating with cross-functional teams on investigations and nonconformances. #J-18808-Ljbffr

Nuclein, LLC is seeking a Quality Control Supervisor in the Austin, TX area to lead QC personnel, train staff, and ensure testing and inspection meet stringent quality standards for diagnostic devices and components. The role emphasizes applying rigorous QC methods, maintaining GMP standards, and driving continuous improvement while collaborating with cross-functional teams on investigations and nonconformances. #J-18808-Ljbffr

Fluor is seeking a Site Quality Lead Auditor to supervise the site quality program, overseeing audits, inspections and documentation across multiple disciplines and shifts. The role requires a technical diploma and extensive construction QA/QC experience to ensure project compliance with contract requirements. Preferred certifications and strong communication skills are recommended. The position involves guiding Quality personnel, coordinating with site management, and contributing to a safe, #J-18808-Ljbffr

West Pharmaceutical Services is seeking a QC Supervisor for an onsite role in Tempe, AZ. You will lead a quality control team, ensure adherence to cGMP and ISO standards, and drive corrective actions. The role emphasizes safety, schedule adherence, and collaboration with cross‑functional teams to maintain product quality. You will oversee inspectors, manage timekeeping, and respond to nonconformances, while supporting site initiatives and training programs. #J-18808-Ljbffr

West Pharmaceutical Services is seeking a QC Supervisor for an onsite role in Tempe, AZ. You will lead a quality control team, ensure adherence to cGMP and ISO standards, and drive corrective actions. The role emphasizes safety, schedule adherence, and collaboration with cross‑functional teams to maintain product quality. You will oversee inspectors, manage timekeeping, and respond to nonconformances, while supporting site initiatives and training programs. #J-18808-Ljbffr

Quality Auditor SupervisorThis is an onsite position requiring the team member to be onsite 5 days a week. No relocation is provided for this opportunity. At West, we're a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life-saving and life-enhancing injectable medicines to millions of patients daily, West's indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There's no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving...

Description This is an onsite position requiring the team member to be onsite 5 days a week. No relocation is provided for this opportunity. At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life‑saving and life‑enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to...

Description This is an onsite position requiring the team member to be onsite 5 days a week. No relocation is provided for this opportunity. At West, we’re a dedicated team that is connected by a purpose to improve patient lives that has been at the center of our Company for more than a century. Our story began when Herman O. West solved the problem of supplying penicillin in mass quantities to the US Government during World War 2. Through our work to deliver thousands of life‑saving and life‑enhancing injectable medicines to millions of patients daily, West’s indelible mark on the healthcare industry has just begun. A name started our story. How will yours help write our future? There’s no better place to join an inclusive community of professionals with opportunities for lifelong learning, growth and development. Supported by benefit programs, we empower the physical, mental, emotional and financial health of our team members and their families. We believe in giving back to...

University of Mississippi Medical Center in Jackson, MS, seeks a Supervisor for the Medical Laboratory – Cytology to provide technical leadership and oversee cytology operations. You will support Lab and Pathology Services, ensure efficient, cost-effective testing, and act as a resource for outside laboratories. The role requires a Bachelor's degree in a chemical, physical, or biological science or Medical Technology, plus four years of relevant experience, with current credentials from #J-18808-Ljbffr

Location: Jackson, Mississippi, United StatesCompany: University of Mississippi Medical CenterPosted: 2026-09-07University of Mississippi Medical Center in Jackson, MS, seeks a Supervisor for the Medical Laboratory – Cytology to provide technical leadership and oversee cytology operations. You will support Lab and Pathology Services, ensure efficient, cost-effective testing, and act as a resource for outside laboratories.The role requires a Bachelor's degree in a chemical, physical, or biological science or Medical Technology, plus four years of relevant experience, with current credentials from#J-18808-Ljbffr

Line Supervisor - Medical Transcript - White Plains, NY, Monday to Friday, 8:00 AM to 5:00 PM Pay range: $29.90 - $44.86 / hour Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation. Benefits information: Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours Best-in-class well-being programs Annual, no-cost health assessment program Blueprint for Wellness healthyMINDS mental health program Vacation and Health/Flex Time 6 Holidays plus 1 "MyDay" off FinFit financial coaching and services 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service Employee stock purchase plan Life and disability insurance, plus buy-up option Flexible Spending Accounts Annual...

Position Summary The Clinical Technical Supervisor is responsible for the technical and scientific oversight of the laboratory's daily operations to ensure accurate, reliable, and timely patient test results in accordance with COLA, CLIA, and all applicable federal and state regulations. This position provides direct supervision of testing personnel, ensures compliance with quality assurance and quality control policies, and supports the laboratory's mission to deliver high-quality, patient-centered diagnostic services. The supervisor will also perform occasional bench work as needed or when short-staffed. Essential Duties and Responsibilities Technical Oversight & Quality Assurance Provide day-to-day technical supervision of all laboratory testing in compliance with COLA and CLIA requirements. Ensure that testing systems are properly functioning and providing accurate and timely results. Oversee verification, calibration, and maintenance of laboratory instruments and ensure...

Hamilton Medical in Reno, NV is seeking a Quality Control Supervisor to lead the Quality Control Technicians team. Responsibilities include oversight of inspections, ensuring compliance with good manufacturing practices, and maintaining quality documentation. The ideal candidate will have a Bachelor's degree and at least 4 years of QA or QC experience, along with leadership skills. The position offers a comprehensive benefits package including medical, dental, and a 401k plan. #J-18808-Ljbffr

FORT WALTON BEACH, Ft Walton Bch, FL, US 30+ days ago Requisition ID: 2150 Position Summary The Clinical Technical Supervisor is responsible for the technical and scientific oversight of the laboratory’s daily operations to ensure accurate, reliable, and timely patient test results in accordance with COLA, CLIA, and all applicable federal and state regulations. This position provides direct supervision of testing personnel, ensures compliance with quality assurance and quality control policies, and supports the laboratory’s mission to deliver high-quality, patient-centered diagnostic services. The supervisor will also perform occasional bench work as needed or when short-staffed. --- Essential Duties and Responsibilities Technical Oversight & Quality Assurance Provide day-to-day technical supervision of all laboratory testing in compliance with COLA and CLIA requirements. Ensure that testing systems are properly functioning and providing accurate and timely results....

About Us:Structure Therapeutics develops life‐changing medicines for patients using advanced structure‐based and computational drug discovery technology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical‐stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions.Structure Therapeutics is led by an experienced group of international drug innovators and financed by top-tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and...

Laboratory Technician Perform in all areas involved in pre-analytic, analytic, and post-analytic testing. Maintain the policies and procedures as technical supervisor in assigned areas of the laboratory to ensure that all regulatory requirements are maintained. Perform routine clinical tests, collect blood samples, prepare media, report results. Uphold the organization's vision, mission, and corporate values. Demonstrate understanding of and compliance with organization's policies, procedures, code of conduct and work rules. Essential Functions: Ensure absolute patient identification and match with required test; perform specimen collection, ensuring high customer service and strict attention to accuracy, integrity, and quality Supervise phlebotomist daily performance Prepare samples outsourced to another laboratory, i.e. Quest send-outs. In charge of laboratory safety compliance. Follow established QC program within parameters for acceptable levels of performance,...

ABOUT DLS Diagnostic Laboratory Services, Inc. (DLS) is Hawaii's largest locally owned and operated medical testing laboratory. DLS is considered a leader in the Hawaii, Guam and Saipan communities we serve. As an integral part of the patient care team, DLS uses state of the art testing and value-based informatics to promote optimal patient care and positively impact patient outcomes. SCHEDULE Regular Full-Time Position (Eve/Night) Must be available Monday through Friday, starting as early as 2:00 PM. Must be flexible with schedule changes to meet operational needs. HIRING RANGE $83,320 to $102,717 annual Actual pay commensurate with experience. JOB SUMMARY Supervises employees and operations for the department. Ensures operations meet regulatory requirements. Partners with the manager in hiring, developing and coaching employees. With department Manager, directs supervisory team and the overall operations of the department in support of the company and department mission,...

Job Description Job Description Position Summary The Clinical Technical Supervisor is responsible for the technical and scientific oversight of the laboratory’s daily operations to ensure accurate, reliable, and timely patient test results in accordance with COLA, CLIA, and all applicable federal and state regulations. This position provides direct supervision of testing personnel, ensures compliance with quality assurance and quality control policies, and supports the laboratory’s mission to deliver high-quality, patient-centered diagnostic services. The supervisor will also perform occasional bench work as needed or when short-staffed. --- Essential Duties and Responsibilities Technical Oversight & Quality Assurance · Provide day-to-day technical supervision of all laboratory testing in compliance with COLA and CLIA requirements. · Ensure that testing systems are properly functioning and providing accurate and timely results. · Oversee verification,...

Location: Hazard, Kentucky, United StatesCompany: Appalachian Regional HealthcarePosted: 2026-09-07Location: Hazard, Kentucky, United StatesCompany: Appalachian Regional HealthcarePosted: 2026-09-04Location: Hazard, Kentucky, United StatesCompany: Appalachian Regional HealthcarePosted: 2026-09-02Location: Hazard, Kentucky, United StatesCompany: Appalachian Regional HealthcarePosted: 2026-08-29Location: Hazard, Kentucky, United StatesCompany: Appalachian Regional HealthcarePosted: 2026-08-22Appalachian Regional Healthcare Inc. seeks a Senior Medical Technologist to supervise laboratory departments and ensure accurate test performance. The role requires strong leadership, knowledge of QC, and collaboration with physicians to discuss abnormal results.You will stay current on procedures, coordinate education for staff, and participate in weekend and on-call coverage as needed. Strong regulatory knowledge is essential for compliance.#J-18808-Ljbffr

About Us Structure Therapeutics develops life‑changing medicines for patients using advanced structure‑based and computational drug discovery technology. The company’s platform combines the latest advancements in visualization of molecular interactions, computational chemistry, and data integration to design orally available, superior small molecule medicines that overcome current limitations of biologic and peptide drugs. We are advancing a clinical‑stage pipeline of differentiated treatments focused on chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Structure Therapeutics is led by an experienced group of international drug innovators and financed by top‑tier global life sciences investors. The company completed an initial public offering (IPO) in February 2023. With offices in California and Shanghai, Structure Therapeutics has the benefit of being at the center of life science innovation in both the US and China and...

Summary This position will report to the Medical Writing Department Head and will lead scientific, medical and regulatory writing activities for development projects, ensuring full life-cycle support from clinical study protocols through regulatory submission and post-approval activities, and that documents are written in compliance with all regulations (ICH, GLPs, and GCPs). The professional will also perform the medical writing, QC reviews, and editing of the documents and will be responsible for the management, planning and direction of a team of medical writers. The professional will ensure the timely presentation/dissemination of clinical data from investigational pipeline products according to budget, timelines, strategic publication plans, and tactical approaches; and ensures that strategically aligned scientific communication points are delivered and that statements and conclusions in publications (manuscripts, abstracts, posters, oral presentations, etc.) are accurate and...