Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

QA Specialist

SWM International

Mativ is a global leader in specialty materials headquartered in Alpharetta, Georgia. The Company offers a wide range of critical components and engineered solutions that connect, protect, and purify our world. This position will check the implementation of the quality system, conduct quality assurance audits, and monitor and record results of processes and procedures against manufacturing standards. Continually compares results to predetermined expected ranges and takes corrective measures if any deviation is found. Responsibilities Responsible for the site equipment calibration and maintenance program Ensures effective oversight of the product stability program, including monitoring, trending, and reporting stability data to support product quality, regulatory compliance, and lifecycle management Own and oversee the site Product Stability Program in alignment with cGMP, FDA, and applicable regulatory requirements Develop, maintain, and execute product stability protocols (initial, ongoing, and accelerated studies as applicable) Ensure stability studies are conducted within defined environmental conditions (temperature, humidity, light exposure where applicable) Coordinate stability sample pulls, testing schedules, and sample inventory management Review and approve stability test results, ensuring compliance with predefined specifications and acceptance criteria Perform statistical trending and analysis of stability data to identify adverse trends, shifts, or out-of-specification conditions Lead stability-related investigations, including OOS, OOT, and atypical results Assess the impact of stability results on product shelf life, expiration dates, and product quality Generate stability summaries and reports for Annual Product Reviews (APR/PQR), regulatory submissions, and internal management review Maintain stability chambers and ensure calibration, qualification, and monitoring of environmental conditions Collaborate with R&D, Quality Control, and Regulatory teams on stability requirements for new products, product changes, and validations Ensure data integrity, documentation accuracy, and audit readiness of all stability records Work with manufacturing staff on quality-related issues Assist with validations/product testing Perform statistical process control and assist with verification of process control performed by others Review cGMP documents to ensure company processes comply (DHRs, Batch Records) Monitor production practices to ensure compliance with the Quality Control procedure Assist production staff where necessary regarding Quality Control procedures and issues Complete documentation to show that tests have been carried out and recording whether the product met the standards or not Compile test measurements and outcomes into reports for inclusion in Annual Product Reviews or Monthly Reports Perform and assist in investigations regarding customer complaints Participate in audits (as needed) Assist in performing corrective actions for audit findings Ensure new products and changes to existing products are carried out through the production process within specification Assist in implementing procedures and specifications for Quality Control Inspectors and Quality Control Lab Technicians Qualifications Required Two years of experience in medical devices, pharmaceuticals, manufacturing, or other related industries Microsoft Office competence Preferred Analytical skills Organizational skills Excellent written communication skills Interpersonal skills Keen attention to detail Critical/logical thinking Proficient in Microsoft Office Suite What We Offer Mativ benefits say a lot about how we care for each other. Our employees and their families have many different needs. As a result, our benefits offer choices on many levels and are high in quality, competitive in the marketplace, and affordable. About Mativ Mativ Holdings, Inc. is a global leader in specialty materials headquartered in Alpharetta, Georgia. The company connects, protects, and purifies the world every day through a wide range of critical components and engineered solutions that solve our customers' most complex challenges. We manufacture on three continents and generate sales in nearly 100 countries through our family of business-to-business and consumer product brands. The company's two segments, Filtration & Advanced Materials and Sustainable & Adhesive Solutions, target premium applications across diversified and growing end-markets, from filtration to healthcare to sustainable packaging and more. Our broad portfolio of technologies combines polymers, fibers, and resins to optimize the performance of our customers' products across multiple stages of the value chain. Our leading positions are a testament to our best-in-class global manufacturing, supply chain, and materials science capabilities. We drive innovation and enhance performance, finding potential in the impossible. #J-18808-Ljbffr

Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the QA Specialist in Knoxville, TN vacancy
  • $19.25 per hour

     ...requirements to other WRMD employees and to participate/assist in their development as needed. Participate in and/or assist with internal QA audits, Customer audits, and Regulatory Agency audits as required. Assist with and/or conduct cGMP training, if requested.... 
    Suggested
    Temporary work
    Weekend work

    Smurfit Westrock plc

    Knoxville, TN
    2 days ago
  • Smurfit Westrock (NYSE:SW) is the go-to leader and partner of choice in sustainable packaging. We are dedicated to creating efficient and scalable paper and packaging solutions to help solve complex packaging challenges. Guided by our values of safety, loyalty, integrity...
    Suggested
    Temporary work
    Immediate start

    Smurfit Westrock plc

    Knoxville, TN
    5 days ago
  • $17 per hour

     ...proactively identify problems with products and goods? In manufacturing and industrial environments, that's what quality assurance (QA) specialists and technicians do best. If you have what it takes to report and verify defects, troubleshoot on the fly and always operate... 
    Suggested
    Temporary work
    Work experience placement
    Immediate start
    Knoxville, TN
    17 days ago
  •  ...Quality Specialist The Quality Specialist will be expected to perform basic quality control functions from subcomponents inspections to finished good dock audits to ensure company products are being produced and distributed with the highest amount of quality, with... 
    Suggested

    Honey Creek Staffing

    Knoxville, TN
    2 days ago
  • $76.44k

    Company Overview Check out this video and find out why our team loves to work here! ( Join Us! CDM Smith – where amazing career journeys unfold. Imagine a place committed to offering an unmatched employee experience. Where you work on projects that are meaningful...
    Suggested
    Contract work
    For contractors
    Work experience placement
    For subcontractor
    H1b
    Immediate start
    Flexible hours

    CDM Smith

    Knoxville, TN
    5 days ago
  • Job Summary The Chief Quality Officer (CQO) is responsible for leading and coordinating quality improvement and performance initiatives throughout the hospital. The CQO ensures compliance with regulatory standards, including The Joint Commission (JC), and serves as ...

    Community Health Systems

    Powell, TN
    1 day ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to QA Specialist. Be the first to apply!