{"schemaVersion":"jobsearcher.job.v1","id":"ae6d2d61e8a8bb55c8306e90","url":"https://jobsearcher.com/jobs/ae6d2d61e8a8bb55c8306e90","canonicalUrl":"https://jobsearcher.com/jobs/ae6d2d61e8a8bb55c8306e90","title":"Quality Supervisor","description":"Medisca is a global company leveraging strong partnerships to serve healthcare professionals across diverse wellness disciplines. Offering extensive and essential solutions - including pharmaceutical ingredients and service, mixing technology manufacturing, analytical testing, and education – Medisca is bridging the gaps in healthcare with an unwavering commitment to precision, innovation, and societal impact.\nThe Quality Supervisor is responsible for supervising the operations of all quality related aspects within the Quality department throughout daily operations ensuring compliance with current Good Manufacturing Practices. This role provides direct supervision of quality personnel, supporting production activities, drives continuous improvement initiatives. This individual will have a team of direct reports. This role reports directly to the Quality Manager.\nLocation: Irving, Texas\nOpportunity\nResponsibilities & Duties:\nQuality\nMaterial Inspection and Release Process\nOversee the inspection and release process of incoming material.\nSupport the technical inquiries with external third party testing laboratories.\nCoordinate sampling activities\nReview and Approval of Standard Operating Procedures\nCollaboration on MEDISCA’s Standard Operating Procedures.\nEnsure Standard Operating Procedures are aligned with external regulations that govern the compounding industry.\nProduction Process\nOversee the production activities related to re-packaging processes.\nQuality Events\nPerform and support deviation investigations, non-conformance material report (NCMR) and corrective and preventative actions (CAPA) investigations as applicable.\nIdentify scientifically sound root causes and implement robust CAPAs.\nEnvironmental Monitoring and Equipment\nOversee the environmental monitoring program in the facility.\nOversee the equipment calibration and maintenance program.\nQuarantine\nMaintenance of quarantine, rejection, rework and return to supplier areas.\nPeriodically review all materials within and ensure timely dispositions are occurring.\nChange Control Process\nSupport the change control process related to the Quality department.\nCollaborate in the quality assessment CRs and provide comprehensive feedback.\nQuality Metrics\nGenerate the KPIs related to the performance of the team.\nCollaborate to the continuous improvement in the department.\nPeople Leadership\nEnsure team members understand and follow cGMPs and MEDISCA policies and procedures.\nLead members of your team; guide them to perform at their best. Set and manage clear targets and KPIs and monitor progress.\nFoster a high driven culture within your team by empowering them to bring their best selves to work.\n\nQualifications\nBachelor's degree or higher in Science\n3-5 years in quality and/or Regulatory Affairs\nKnowledge of cGMPs, 21 CFR Part 211, GUI-0104, GUI-0069; ICH Guidelines; ISO 9001; ISO 13485.\nPrevious experience in supervision and/or management, with a strong leadership presence.\nExcellent communication skills required; fluent English & French (oral & written). This position interfaces with facilities in the Unites States and Australia.\nAnalytical, with the ability to make data & people driven decisions.\nGreat time & project management skills.\nVery good command of Microsoft Office (Word, Excel, Outlook)\nExperience with MasterControl is a strong asset\n\nWhat’s in it for you…\nWe invest time and resources into making sure Medisca is as good as the people we hire.\nWork/Life Balance – PTO, vacation policy and paid statutory holidays\nInvest in your health – Group Benefit plan and health savings account\nYour Future is Bright – Opportunities to learn and grow within Medisca\nSave for your Future – Medisca contributes to a 401k plan when you invest in the plan\nHelp us grow – Employee Referral Program\nWe like to have fun – company events throughout the year\nFull time positions - 40 hour work week\nYour safety is important – Medisca provides an allocation to purchase safety shoes\nCompany is growing - new state of the art facility, coming soon\n\nWe thank all applicants for their interest; however, only candidates to be interviewed will be contacted.\nWe are an equal opportunity employer.\n#LI-Onsite\nEqual Opportunity Employer\nThis employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.","company":"Medisc","rawCompany":"medisc","city":"Arlington","state":"TX","isRemote":false,"isActive":false,"createdAt":"2026-08-03T15:56:26.730Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"51-1011.00","title":"First-Line Supervisors of Production and Operating Workers","slug":"first-line-supervisors-of-production-and-operating-workers"}],"industries":[{"code":"325412","title":"Pharmaceutical Preparation Manufacturing","slug":"pharmaceutical-preparation-manufacturing"},{"code":"325414","title":"Biological Product (except Diagnostic) Manufacturing","slug":"biological-product-except-diagnostic-manufacturing"},{"code":"325411","title":"Medicinal and Botanical Manufacturing","slug":"medicinal-and-botanical-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Supervisor","description":"Medisca is a global company leveraging strong partnerships to serve healthcare professionals across diverse wellness disciplines. Offering extensive and essential solutions - including pharmaceutical ingredients and service, mixing technology manufacturing, analytical testing, and education – Medisca is bridging the gaps in healthcare with an unwavering commitment to precision, innovation, and societal impact.\nThe Quality Supervisor is responsible for supervising the operations of all quality related aspects within the Quality department throughout daily operations ensuring compliance with current Good Manufacturing Practices. This role provides direct supervision of quality personnel, supporting production activities, drives continuous improvement initiatives. This individual will have a team of direct reports. This role reports directly to the Quality Manager.\nLocation: Irving, Texas\nOpportunity\nResponsibilities & Duties:\nQuality\nMaterial Inspection and Release Process\nOversee the inspection and release process of incoming material.\nSupport the technical inquiries with external third party testing laboratories.\nCoordinate sampling activities\nReview and Approval of Standard Operating Procedures\nCollaboration on MEDISCA’s Standard Operating Procedures.\nEnsure Standard Operating Procedures are aligned with external regulations that govern the compounding industry.\nProduction Process\nOversee the production activities related to re-packaging processes.\nQuality Events\nPerform and support deviation investigations, non-conformance material report (NCMR) and corrective and preventative actions (CAPA) investigations as applicable.\nIdentify scientifically sound root causes and implement robust CAPAs.\nEnvironmental Monitoring and Equipment\nOversee the environmental monitoring program in the facility.\nOversee the equipment calibration and maintenance program.\nQuarantine\nMaintenance of quarantine, rejection, rework and return to supplier areas.\nPeriodically review all materials within and ensure timely dispositions are occurring.\nChange Control Process\nSupport the change control process related to the Quality department.\nCollaborate in the quality assessment CRs and provide comprehensive feedback.\nQuality Metrics\nGenerate the KPIs related to the performance of the team.\nCollaborate to the continuous improvement in the department.\nPeople Leadership\nEnsure team members understand and follow cGMPs and MEDISCA policies and procedures.\nLead members of your team; guide them to perform at their best. Set and manage clear targets and KPIs and monitor progress.\nFoster a high driven culture within your team by empowering them to bring their best selves to work.\n\nQualifications\nBachelor's degree or higher in Science\n3-5 years in quality and/or Regulatory Affairs\nKnowledge of cGMPs, 21 CFR Part 211, GUI-0104, GUI-0069; ICH Guidelines; ISO 9001; ISO 13485.\nPrevious experience in supervision and/or management, with a strong leadership presence.\nExcellent communication skills required; fluent English & French (oral & written). This position interfaces with facilities in the Unites States and Australia.\nAnalytical, with the ability to make data & people driven decisions.\nGreat time & project management skills.\nVery good command of Microsoft Office (Word, Excel, Outlook)\nExperience with MasterControl is a strong asset\n\nWhat’s in it for you…\nWe invest time and resources into making sure Medisca is as good as the people we hire.\nWork/Life Balance – PTO, vacation policy and paid statutory holidays\nInvest in your health – Group Benefit plan and health savings account\nYour Future is Bright – Opportunities to learn and grow within Medisca\nSave for your Future – Medisca contributes to a 401k plan when you invest in the plan\nHelp us grow – Employee Referral Program\nWe like to have fun – company events throughout the year\nFull time positions - 40 hour work week\nYour safety is important – Medisca provides an allocation to purchase safety shoes\nCompany is growing - new state of the art facility, coming soon\n\nWe thank all applicants for their interest; however, only candidates to be interviewed will be contacted.\nWe are an equal opportunity employer.\n#LI-Onsite\nEqual Opportunity Employer\nThis employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights (https://www.eeoc.gov/poster) notice from the Department of Labor.","datePosted":"2026-08-03T15:56:26.730Z","dateModified":"2026-08-03T15:56:26.730Z","hiringOrganization":{"@type":"Organization","name":"Medisc","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Arlington","addressRegion":"TX","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"ae6d2d61e8a8bb55c8306e90"},"url":"https://jobsearcher.com/jobs/ae6d2d61e8a8bb55c8306e90"}}