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The QC Supervisor leads and develops a team of QC inspectors to deliver on-time QC activities and uphold GMP compliance while meeting customer expectations and regulatory demands. Responsibilities cover team management, floor engagement, audit-ready cGMP documentation, recruitment, coaching, escalation support, safety data sheet assessment, GMP documentation review, investigations and CAPA follow-up, quality oversight for assigned projects, reporting GMP breaches, and maintaining QC administrative duties including coverage beyond normal hours and international travel.",{"@graph":63,"@context":119},[64,80,102],{"@type":65,"itemListElement":66},"BreadcrumbList",[67,71,74,77],{"item":68,"name":69,"@type":70,"position":9},"https://docshare.wps.com","Home","ListItem",{"item":72,"name":10,"@type":70,"position":73},"https://docshare.wps.com/template/",2,{"item":75,"name":16,"@type":70,"position":76},"https://docshare.wps.com/template/resumes/",3,{"item":78,"name":59,"@type":70,"position":79},"https://docshare.wps.com/template/quality-control-supervisor-job-description-july-2023/259574/",4,{"url":78,"name":59,"@type":81,"image":82,"author":87,"headline":59,"publisher":90,"fileFormat":93,"inLanguage":57,"description":61,"dateModified":94,"datePublished":95,"encodingFormat":93,"isAccessibleForFree":96,"interactionStatistic":97},"DigitalDocument",{"url":83,"@type":84,"width":85,"height":86},"https://docshare.wps.com/thumbnails/quality-control-supervisor-job-description-july-2023/259574.png","ImageObject",442,249,{"name":88,"@type":89},"8796093062539","Person",{"url":68,"name":91,"@type":92},"DocShare","Organization","application/pdf","2026-10-21","2026-09-13",true,{"@type":98,"interactionType":99,"userInteractionCount":101},"InteractionCounter",{"@type":100},"ViewAction",6,{"@type":103,"mainEntity":104},"FAQPage",[105,111,115],{"name":106,"@type":107,"acceptedAnswer":108},"What is the overall role objective of the QC Supervisor?","Question",{"text":109,"@type":110},"To manage and develop a QC team to ensure timely QC activities, uphold GMP compliance principles, and support the business in line with customer expectations and regulatory demands.","Answer",{"name":112,"@type":107,"acceptedAnswer":113},"Which main responsibilities fall under supervisor duties?",{"text":114,"@type":110},"Managing and developing direct reports, monitoring workload and performance, maintaining regular floor presence, reviewing team documentation for cGMP compliance, meeting for feedback and assessment, and recruiting educated personnel with sufficient capacity.",{"name":116,"@type":107,"acceptedAnswer":117},"What technical duties does the QC Supervisor perform?",{"text":118,"@type":110},"Assessing safety data sheets and suitability of products before processing, reviewing and approving GMP documentation, quotes and invoices, supporting investigations and root cause analysis, ensuring CAPA actions are completed timely, and acting as a GxP quality representative/SME for assigned projects.","https://schema.org",{"og:url":78,"og:type":121,"og:title":59,"og:site_name":91,"og:description":61},"article",{"robots":123,"canonical":78},"index,follow",{"doc_id":125,"site_id":56},259574,1790354791,{"code":4,"msg":5,"data":128},{"doc_id":125,"user_id":129,"nickname":88,"user_avatar":60,"doc_module":9,"category_id":15,"category_name":16,"doc_title":59,"doc_description":61,"doc_content":130,"file_id":131,"file_url":132,"file_type":133,"file_size":134,"view_count":101,"is_deleted":4,"is_public":9,"is_downloadable":9,"audit_status":9,"page_count":47,"language":135,"language_code":57,"site_id":56,"html_lang":57,"table_of_contents":136,"faqs":137,"seo_title":138,"seo_description":61,"update_tm":139,"read_time":73},8796093062539,"JOB DESCRIPTION  \n\n| JOB DESCRIPTION CREATION DATE: | 11 Jul 2023 |\n| --- | --- |\n| POSITION: | CS CR QC Supervisor\u003Cbr>Assigned to any of the following areas: Label Control / Distribution\u003Cbr>Materials Production |\n| BUSINESS UNIT: | Clinical Services |\n| LOCATION: | Craigavon |\n| REPORTING TO: | CS CR Quality Control Manager |\n| RESPONSIBLE FOR (PEOPLE): | CS CR QC Inspectors\u003Cbr>(assigned to the respective area) |\n\nOVERALL ROLE OBJECTIVE:  \nThe QC Supervisor is responsible for the management and development of a team to ensure on-time delivery of QC activities necessary to monitor and uphold the principles of GMP compliance and support the business in line with customer expectations and regulatory demands. 1  \n1 These activities may be performed for any Almac site.  \nJOB SPECIFIC RESPONSIBILITIES:  \nThe post holder will:  \nSupervisor Duties  \n1. Manage a team of personnel , foster a positive working environment and be accountable for the performance of your direct reports. Closely monitor workload associated with tasks associated with the area to which they are assigned to undertake at any site. Provide good visibility of output and performance.  \n2. Maintain a regular presence on the floor , engaging with personnel to understand challenges , issues, trends and areas where change is necessary. Frequently review documentation completed by the team in order to monitor performance, quality , consistency and compliance with cGMP. Ensure QC related documentation is audit/ inspection ready at all times.  \n3. Meet regularly with your team throughout the year and also via the assessment process. Provide feedback , promoting staff engagement and development and address issues when performance is falling short of expectations in accordance with HR policies.  \n4. Recruit new team members, ensuring there is sufficient , educated personnel available to perform the tasks in accordance with business and customer timelines.  \n5. Support, coach and mentor team members to apply knowledge gained to perform QC activities and empower decision-making in order to build on their competence and experience. Ensure training records are up-to-date.  \n6. Act as first point of escalation and provide advice to Project Services and operational staff to resolve issues. Highlight to the QC Manager as appropriate.  \nTechnical Duties  \n7. Update register of materials processed by Clinical Services by assessing Safety Data Sheets. Ensure products are suitability assessed before processing and that appropriate handling procedures are in place by identifying any hazards and controlling risks. 1  \n8. Review and approve GMP documentation , quotes and invoices in accordance with the relevant procedures.1  \n9. Support the Lead Investigator during the conduct of investigations and root cause analysis.  \n10. Ensure any CAPA / Follow-up actions assigned to you or your direct reports are actioned in a timely manner.  \n11. Act as a Quality representative / Subject Matter Expert on assigned projects, providing advice and guidance from a GxP perspective. 1  \n• This task may be delegated by the QC Manager  \n12. Continuously consider opportunities for business improvement and be forthcoming with ideas/ suggestions regarding process simplification and improved compliance. Support the implementation of such via engagement in SOP updates and action items arising from initiativesand projects. Ensure good engagement with global counterparts in order to gain agreement (as required) . 1  \n1 These activities may be performed for any Almac site.  \nGeneral Duties  \n13. Report / escalate serious / potentially serious breaches of GMP compliance or matters of concern such as challenges / barriers or resource constraints to the QC Managers in an open and timely manner for appropriate resolution.  \n14. Assist management in the preparation and delivery of data for customer / supplier teleconferences / meetings , as needed , representing the QC department.  \n15. Maintain oversight of service pr","cbCaipZtXEAqSW7S","https://ap.wps.com/l/cbCaipZtXEAqSW7S","pdf",137574,"English","# Role Objective\n# Job Specific Responsibilities\n## Supervisor Duties\n## Technical Duties\n## General Duties\n# General Role Responsibilities\n## Quality\n## Health & Safety\n## Training and Development\n## Human Resource Management\n## Communication\n## Equal Opportunities\n## Core Competency Framework\n# Acknowledgement and Sign-off","[{\"question\":\"What is the overall role objective of the QC Supervisor?\",\"answer\":\"To manage and develop a QC team to ensure timely QC activities, uphold GMP compliance principles, and support the business in line with customer expectations and regulatory demands.\"},{\"question\":\"Which main responsibilities fall under supervisor duties?\",\"answer\":\"Managing and developing direct reports, monitoring workload and performance, maintaining regular floor presence, reviewing team documentation for cGMP compliance, meeting for feedback and assessment, and recruiting educated personnel with sufficient capacity.\"},{\"question\":\"What technical duties does the QC Supervisor perform?\",\"answer\":\"Assessing safety data sheets and suitability of products before processing, reviewing and approving GMP documentation, quotes and invoices, supporting investigations and root cause analysis, ensuring CAPA actions are completed timely, and acting as a GxP quality representative/SME for assigned projects.\"}]","Quality Control Supervisor Job Description - July 2023 | PDF",1789334190]