| Location | Knoxville |
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.ResponsibilitiesResponsible for the site equipment calibration and maintenance programEnsures effective oversight of the product stability program, including monitoring, trending, and reporting stability data to support product quality, regulatory compliance, and lifecycle managementOwn and oversee the site Product Stability Program in alignment with cGMP, FDA, and applicable regulatory requirementsDevelop, 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 managementReview and approve stability test results, ensuring compliance with predefined specifications and acceptance criteriaPerform statistical trending and analysis of stability data to identify adverse trends, shifts, or out-of-specification conditionsLead stability-related investigations, including OOS, OOT, and atypical resultsAssess the impact of stability results on product shelf life, expiration dates, and product qualityGenerate stability summaries and reports for Annual Product Reviews (APR/PQR), regulatory submissions, and internal management reviewMaintain stability chambers and ensure calibration, qualification, and monitoring of environmental conditionsCollaborate with R&D, Quality Control, and Regulatory teams on stability requirements for new products, product changes, and validationsEnsure data integrity, documentation accuracy, and audit readiness of all stability recordsWork with manufacturing staff on quality-related issuesAssist with validations/product testingPerform statistical process control and assist with verification of process control performed by othersReview cGMP documents to ensure company processes comply (DHRs, Batch Records)Monitor production practices to ensure compliance with the Quality Control procedureAssist production staff regarding Quality Control procedures and issuesComplete documentation to show that tests have been carried out and record whether the product met the standards or notCompile test measurements and outcomes into reports for inclusion in Annual Product Reviews or Monthly ReportsPerform and assist in investigations regarding customer complaintsParticipate in audits (as needed) and assist in performing corrective actions for audit findingsEnsure new products and changes to existing products are carried out through the production process within the specificationAssist in implementing procedures and specifications for Quality Control Inspectors and Quality Control Lab TechniciansQualificationsRequired: Two years of experience in medical devices, pharmaceuticals, manufacturing, or other related industriesRequired: Microsoft Office competencePreferred: Analytical skillsPreferred: Organizational skillsPreferred: Excellent written communication skillsPreferred: Interpersonal skillsPreferred: Keen attention to detailPreferred: Critical/logical thinkingPreferred: Proficient in Microsoft Office SuiteWHAT WE OFFERMativ benefits support employees and their families with high-quality, competitive, and affordable options.ABOUT MATIVMativ Holdings, Inc. is a global leader in specialty materials. We connect, protect, and purify the world through a wide range of components and engineered solutions. We operate on three continents and serve nearly 100 countries, with brands across business-to-business and consumer markets. Our segments focus on premium applications across diversified markets, including filtration, healthcare, and sustainable packaging.#J-18808-Ljbffr