39 clinical and health jobs found

Position Summary Shift: Monday-Friday 8am-5pm 100% on-site Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply products that help people live better and healthier lives. Catalent is dedicated to delivering unparalleled service to pharma, biotech, and consumer health customers, supporting product development, launch, and full life-cycle supply. With time-tested experience in development sciences, delivery technologies, and multi-modality manufacturing, Catalent supports the acceleration of development programs and the launch of more than a hundred new products every year. Powered by thousands of scientists and technicians and the latest technology platforms at more than 40 global sites, Catalent supplies billions of doses of life-enhancing and life-saving treatments for patients annually. Catalent’s Kansas City facility is home to our Oral & Specialty Drug Delivery,...

SCHOOL WIDE RESEARCH (IN-RESW-IUINA) The Quality Assurance (QA) Director is responsible for leading the Indiana University School of Medicine (IUSM) Quality Assurance organization and for supporting various areas across Indiana University (IU) including Cell and Gene Therapy Manufacturing, Gene Therapy Testing Laboratory, IU Genetics Biobank, Laboratory Animal Resource Center, Biospecimen Management Core, and Clinical Research Center. Additionally, the Quality Director is responsible for providing strategic quality support to broad-reaching initiatives such as the Quality and Compliance Workstream as part of the IU Health Clinical Research Council and to Indiana's Clinical Translational Science Institute. Department-Specific Responsibilities Provides quality leadership support. Interacts closely with leadership and departments across IUSM and IU Health to understand strategies, feedback and future needs in order to partner with them in establishing and implementing quality...

Join us in pioneering breakthroughs in healthcare. For everyone. Everywhere. Sustainably. Our inspiring and caring environment forms a global community that celebrates diversity and individuality. We encourage you to step beyond your comfort zone, offering resources and flexibility to foster your professional and personal growth, all while valuing your unique contributions. Varian Medical Systems, a Siemens Healthineers company is hiring for a Design Quality Assurance Specialist in one of the 2 following locations (Shoreview, MN or Austin, TX). In this role you will be accountable for the design and development processes, ensuring specific controls are in place and documented to meet adequate quality at all product realization stages. You will keep abreast of regulatory procedures and changes to ensure compliance throughout the complete product life cycle. In addition, you will support the QT team in internal and external audits and work in close collaboration with other...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Catalent Inc. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Quality Assurance Document Control Position Summary Work Schedule: Monday – Friday, 3:45pm to 12:15am 100% on-site Catalent’s 206,878-square-foot Philadelphia-area facility serves as the global Center of Excellence for Clinical Supply Packaging, offering GMP secondary packaging and clinical labeling services. The site provides manual to fully automated packaging solutions, including temperature-controlled options for sensitive products. Come and be part of a team...

Job Title: Quality Assurance Specialist Job Description This role involves providing comprehensive support in quality-related tasks, including daily inquiries, policy interpretation, routine monitoring, audit preparation, corrective actions, and more. One specialist will focus on audits and audit preparation, while the other will concentrate on education and training tasks. A thorough understanding of protocol review/execution, documentation, adherence schedules, site workflows, and regulatory processes is essential. Responsibilities Support the Cancer, Clinical Trials, and Translational Research Office with quality-related tasks. Handle daily inquiries and interpret policies. Monitor routine activities and prepare for audits. Implement corrective actions when necessary. Focus on audit preparation and educational/training tasks. Understand and execute protocol reviews and documentation. Maintain schedules of adherence and manage site workflows. Ensure compliance...

NY HELP Yes Agency Health, Department of Title Call Center Quality Assurance Specialist 1 (NY HELPS) - 79990 Occupational Category Other Professional Careers Salary Grade 18 Bargaining Unit PS&T - Professional, Scientific, and Technical (PEF) Salary Range From $66951 to $85138 Annually Employment Type Full-Time Appointment Type Permanent Jurisdictional Class Competitive Class Travel Percentage 0% Workweek Mon-Fri Hours Per Week 37.5 Workday From 9 AM To 5 PM Flextime allowed? No Mandatory overtime? No Compressed workweek allowed? Yes Telecommuting allowed? Yes County New York Street Address Division of Eligibility and Marketplace Integration/ Bureau of Quality Management and Change Control Corporate Woods 22 City Albany State NY Zip Code 12211 Duties Description Responsibilities: This Call Center Quality Assurance Specialist 1 within the Division of Eligibility and Marketplace Integration, Bureau of Quality Management will...

Job Title: Quality Assurance Associate Job Description We are seeking a dedicated Quality Assurance Associate to support on-the-floor QA issues within our manufacturing suite. You will play a crucial role in mitigating gaps and risks for all quality and GMP processes, and will run investigations for deviations, change controls, CAPAs, and out-of-specifications. Additionally, you will review and author SOPs to ensure compliance with industry standards. Responsibilities Support on-the-floor QA issues within the manufacturing suite. Mitigate gaps and risks for all quality and GMP processes. Conduct investigations for deviations, change controls, CAPAs, and out-of-specifications. Review and author Standard Operating Procedures (SOPs). Essential Skills Proficiency in quality assurance and document control. Experience with batch record review, CAPA, and deviation management. Knowledge of compliance, audits, and quality systems management. Familiarity with cGMP,...

We’re Cubby Beds 👋 A fast-growing and high-impact startup that makes smart beds for people with cognitive conditions like Epilepsy, Cerebral Palsy, Dementia and Autism. Our mission is to improve the lives of special needs kids and their families through our innovative products and go to market strategies. Since launch, we have changed the lives of thousands of families, been insurance covered in all 50 states, achieved profitability, and are building a growing team in our Denver HQ. The next stage of the business is all about scaling our team, product, systems, and customer journey to help thousands more families get the safe sleep they deserve. This is where you come in When you join Cubby, you’re joining a team of passionate, talented individuals on a mission to change the lives of thousands of special needs families. As we continue to grow at lightning speed, we are seeking a detail-oriented and systems-minded quality professional who takes pride in helping build and...

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day. 3rd shift Quality Assurance Pay Rate $18-20 hr Quality Assurance (QA) is an integral part of operations at the Lynnfield, MA Innovation Center. Every employee at the center is responsible for ensuring we deliver quality in all that we do.? The Quality Director and Quality Supervisor, who in turn direct the QA Team to conduct daily Quality Assurance inspection, manage the production QA effort.?The overall QA mission is to make sure quality specifications are achieved, and only quality products are released to mail from the facility.? Responsibilities ?Inspecting that overall print...

Perform a wide variety of job functions associated with maintaining inventory integrity and improving efficiencies throughout the distribution center. Essential Job Functions Perform order adjustments (repicks). Monitor, research, and resolve allocation issues in the Problem Resolution (Orders) program. Perform inventory transfers and adjustments as needed. Print and apply location label requests. Request repair and replacement of RF and Vocollect units. Review and research various reports. Research inventory discrepancies and explains large quantity on hand adjustments. Perform all jobs functions associated with processing stray parts. Research and correct item numbers and locations in the LogPro Quantity Correction program. Audit outbound parcels and inbound license plates daily and verify results. Perform daily audits and reconcile all items located in damage locations. Perform all job functions associated with relabel and changeover projects which includes...

HIRING NOW: Quality Assurance Documentation Associate Interested in this role? Reach out directly to apply TODAY to Grace Williams at grawilliams@actalentservices .com (grawilliams@actalentservices.com) | Call/Text 317-567 6610 Summary As a QA Associate, you will play a crucial role in ensuring the quality and compliance of our products and packaging. You will be responsible for reviewing and analyzing data, supporting quality systems, and ensuring adherence to applicable procedures and standards. Responsibilities Provide support to Quality systems. Organize, critically review, and present information in accordance with written procedures. Provide support for the production area. Apply and obtain statistical analysis. Write, review, and revise GMP standard operating procedures. Track, maintain, and critically review manufacturing records. Maintain communication with QC lab regarding test results pertinent to batch release....

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day. 3rd shift Quality Assurance Pay Rate $18-20 hr Quality Assurance (QA) is an integral part of operations at the Lynnfield, MA Innovation Center. Every employee at the center is responsible for ensuring we deliver quality in all that we do. The Quality Director and Quality Supervisor, who in turn direct the QA Team to conduct daily Quality Assurance inspection, manage the production QA effort. The overall QA mission is to make sure quality specifications are achieved, and only quality products are released to mail from the facility. Responsibilities Inspecting that...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Lockheed Martin Corporation. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Description What We're Doing Our team, Command and Control, Battle Management and Communications (C2BMC)- Global team at Lockheed Martin, is dedicated to engineering, developing, and integrating new capabilities for the Missile Defense System that protects the United States and its allies. While we are part of a large organization, we operate within smaller, agile teams in a fast-paced, dynamic environment. Our responsibilities include Sensor/Weapon...

Job Title: Quality Assurance Technician Job Description Join our dynamic team as a Quality Assurance Technician, where you will play a crucial role in ensuring the quality and compliance of our products. You will utilize lab equipment to test finished products and components, ensuring they meet specified parameters. This position offers the opportunity to work in a rapidly growing company with a family-like culture. Responsibilities Operate lab equipment to test finished products and components, ensuring compliance with specified parameters. Conduct multiple process checks throughout production, packaging, and warehousing functions. Set up and calibrate HPLC and GC testing equipment. Receive, document, and log batch testing results into specified systems. Analyze and report quality results to supervisors and managers. Perform physical property testing using various instrumentation. Provide independent oversight of lab processes and verify compliance with company...

Job Title: Quality Assurance Laboratory Technician Job Description We are seeking a dedicated Quality Assurance Laboratory Technician to join our team. This role operates on a 2-2-3 schedule from 6 PM to 6:30 AM, requiring adaptability as the schedule changes weekly. Approximately 75% of your time will be spent on the floor, with the remaining 25% dedicated to testing tasks. Your day will start by checking emails and reviewing a list of tasks to complete. Responsibilities Swab machinery to check for contamination and conduct antibiotic testing. Run samples and perform line checks. Conduct microbiological evaluations of all raw, pasteurized, and final products. Operate equipment such as spectrometers, FTIR analyzers, moisture analyzers, and pH meters. Perform daily quality audits and checks on the plant floor, documenting findings. Recognize and report any unusual results or product defects to the Quality Assurance Lead and Manager....

Biologics Quality Assurance Specialist INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW! ? Job Description The Quality Assurance (QA) Auditor provides compliance and quality improvement support to the manufacture of phase 1/2a Investigational New Drug, Biologics manufacture, and facility operations. This role collaborates with the Quality Assurance Manager to plan, schedule, and conduct audits and administrative tasks to support the quality management program. The position ensures compliance with applicable regulations, policies, procedures, and expectations of phase-appropriate current Good Manufacturing Practices (cGMP). The QA Auditor I will also engage in various quality improvement and process improvement initiatives. Responsibilities Operate within the Quality Management Systems applicable to Investigational New Drugs and Good Tissue Practices. Maintain a...

INTERESTED CANDIDATES CAN SEND UPDATED RESUMES TO MAMCDONOUGH @ACTALENTSERVICES .COM OR TEXT MARISA AT 330. 397. 1302 TO SET UP A PHONE INTERVIEW! Job Description The Quality Assurance (QA) Auditor provides compliance and quality improvement support to the manufacture of phase 1/2a Investigational New Drug, Biologics manufacture, and facility operations. This role collaborates with the Quality Assurance Manager to plan, schedule, and conduct audits and administrative tasks to support the quality management program. The position ensures compliance with applicable regulations, policies, procedures, and expectations of phase-appropriate current Good Manufacturing Practices (cGMP). The QA Auditor I will also engage in various quality improvement and process improvement initiatives. Responsibilities Operate within the Quality Management Systems applicable to Investigational New Drugs and Good Tissue Practices. Maintain a current knowledge of applicable...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for Compass Group, North America. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Fresh & Ready Foods We are hiring immediately for a XXX position. Location : Note: online applications accepted only . Schedule : Requirement : Pay Range: [[cust_StartingPayRate]] per hour to [[cust_MaxPayRate]] per hour. *Internal Employee Referral Bonus Available We Make Applying Easy! Just text JOB to 75000 & search for the requisition ID number 1504363 . The advertised program is a conversational recruiting assistant that helps...

Description We are seeking an experienced FSQA Technician to join our team. The desired candidate will possess strong attention to detail, excellent problem-solving skills, and the ability to work effectively within a fast-paced environment. Why YOU should work for us! Competitive wages and paid time off plans Robust benefits package offered 1st of the month following 30 days: Medical, vision, and dental insurance Company paid basic life insurance and AD&D coverage with additional supplemental coverage available Critical Illness and Voluntary Accident coverage available Associate Purchase Program: product purchase at discounted rate Other wonderful benefits available: Tuition Reimbursement Paid Holidays, plus Floating Holidays Financial coverage provided towards safety footwear 401K Retirement Program with company contribution Gainsharing Incentive Program: Unlimited earning potential when company...

Quality Engineer 1, Product Quality Assurance Date: Feb 11, 2026 Location: Chelmsford, MA, US Company: Teleflex Expected Travel : Up to 10% Requisition ID :13378 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people's lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow, Barrigel, Deknatel, LMA, Pilling, QuikClot, Rüsch, UroLift and Weck - trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit...

Description 1st Shift: 7:00 AM - 3:30 PM, Monday-Friday Position Overview This role involves physical and chemical testing, visual inspections, and overall quality monitoring of plant operations and finished products. Key Responsibilities Perform in-process analytical testing on products manufactured using continuous cooking equipment (e.g., % soluble solids, viscosity, color) as needed. Conduct organoleptic and visual inspections on products in wet-side areas (Oringer, C1-C5, ILF). Audit cook stations and packaging lines to ensure compliance with HACCP food safety protocols, weights, seals, temperatures, codes, and GMPs. Ensure food safety and quality standards for all products produced or packaged daily. Report and initiate corrective actions for any food safety or quality issues. Conduct environmental swabbing of equipment when necessary. Maintain clear communication across production and management teams. Accurately complete all required daily...

Important Recruitment Information for this vacancy Job Posting closes: Open until Filled Required documents uploaded by: All required documents listed below must be attached to your application within 2 days of applying for your application to be considered complete. Agency Information: Kansas Department for Aging and Disability Services Protecting Kansans, Promoting Recovery and Supporting Self Sufficiency https://www.kdads.ks.gov/ About the Position Who can apply: Anyone Classified/Unclassified Service: Unclassified Full-Time/Part-Time: Full-Time Regular/Temporary: Regular Work Schedule: M-F Eligible to Receive Benefits: Yes Veterans' Preference Eligible: Yes Disability Preference Eligible: Yes Search Keywords: Quality Assurance Generalist Compensation: Up to a maximum salary of $55,000 annually. Salary can vary depending upon education, experience, or qualifications....

NY HELP No Agency Information Technology Services, Office of Title Technology Analyst 1 (Quality Assurance) - SP04NYC Occupational Category I.T. Engineering, Sciences Salary Grade 23 Bargaining Unit PS&T - Professional, Scientific, and Technical (PEF) Salary Range From $86681 to $109650 Annually Employment Type Full-Time Appointment Type Temporary Jurisdictional Class Competitive Class Travel Percentage 0% Workweek Mon-Fri Hours Per Week 37.5 Workday From 8 AM To 5 PM Flextime allowed? No Mandatory overtime? No Compressed workweek allowed? No Telecommuting allowed? Yes County To Be Determined Street Address New York City City NYC State NY Zip Code 0 Duties Description The New York State Office of Information Technology Services (ITS) provides operational support 24 hours a day, 7 days a week, 365 days of the year, supporting more than 4,900 applications for 53 New York State Agencies.Under the direction of the Technology...

POSITION SUMMARY Northern New Mexico Integrated Security, located in beautiful northern New Mexico, provides a professional, highly trained protective force that safely secures special nuclear material, people and other critical assets for the Department of Energy, the National Nuclear Security Administration, and the Los Alamos National Laboratory. Northern New Mexico Integrated Security is a subsidiary of Constellis. For additional information regarding this position please contact Barbara Bechechi at bbachechi@lanl.gov or 505-665-8744. Position closes on February 16, 2026, at 7:00 pm EST. The Performance Tester is responsible for planning, coordinating and conducting performance tests as directed by the Performance Testing Manager. The Tester conducts performance assurance and testing activities in accordance with policies, procedures and safety requirements. RESPONSIBILITIES Conduct performance tests as required including Los Alamos National Laboratory (LANL)...