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Quality Assurance Manager

  • ... Posted on: Apr 01, 2026
  • ... Sovrin Medical Plastics
  • ... Slough, null
  • ... Salary: Not Available
  • ... Full-time

Quality Assurance Manager   

Job Title :

Quality Assurance Manager

Job Type :

Full-time

Job Location :

Slough null United States

Remote :

No

Jobcon Logo Job Description :

Quality ManagerSovrin Medical Plastics LtdLocation: UK (on-site)Contract: Full-time, PermanentAbout Sovrin Medical PlasticsSovrin Medical Plastics Ltd is a well-established UK manufacturer specialising in medical device moulding and cleanroom manufacturing. With a long-standing reputation for quality, compliance, and technical excellence, we support leading medical and healthcare customers with precision injection-moulded components and validated manufacturing processes.Operating within a regulated ISO 13485 environment, quality is central to everything we do.The RoleWe are seeking an experienced Quality Manager to lead and continuously improve our Quality Management System and ensure full compliance with ISO 13485 and applicable regulatory requirements.This is a hands-on leadership role, working closely with Operations, Engineering, and Customers to ensure robust processes, effective risk management, and audit readiness at all times.Key ResponsibilitiesOwn, maintain, and develop the ISO 13485 Quality Management SystemAct as site lead for external audits (customers, notified bodies, regulators) and internal auditsManage CAPA, deviations, non-conformances, and complaints through to effective closureEnsure compliance with regulatory and customer requirements for medical device manufactureOversee document control, change control, and validation documentationLead quality input into new product introduction (NPI) and process changesManage supplier quality, including supplier approval and performance monitoringDrive continuous improvement and quality culture across the businessProvide leadership and mentoring to quality team members as their line managerSkills & Experience RequiredProven experience as a Quality Manager (or Senior Quality Engineer) in a manufacturing environmentStrong working knowledge of ISO 13485 (medical devices essential)Experience within plastic injection moulding, cleanroom, or medical manufacturing highly desirableConfident leading audits and interfacing with customers and external bodiesPractical experience of CAPA, risk management, and validation activitiesStrong attention to detail with a pragmatic, solutions-focused mindsetExcellent communication skills at all levelsStrong IT skills for working in a data-driven environment (ERP experience desirable)What We OfferKey leadership role within a respected medical manufacturing businessOpportunity to shape and strengthen quality systems and cultureStable, long-term position in a growing and technically capable organisationCompetitive salary, commensurate with experience

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Jobcon Logo Position Details

Posted:

Apr 01, 2026

Reference Number:

19584_4384177524

Employment:

Full-time

Salary:

Not Available

City:

Slough

Job Origin:

APPCAST_CPC

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Quality ManagerSovrin Medical Plastics LtdLocation: UK (on-site)Contract: Full-time, PermanentAbout Sovrin Medical PlasticsSovrin Medical Plastics Ltd is a well-established UK manufacturer specialising in medical device moulding and cleanroom manufacturing. With a long-standing reputation for quality, compliance, and technical excellence, we support leading medical and healthcare customers with precision injection-moulded components and validated manufacturing processes.Operating within a regulated ISO 13485 environment, quality is central to everything we do.The RoleWe are seeking an experienced Quality Manager to lead and continuously improve our Quality Management System and ensure full compliance with ISO 13485 and applicable regulatory requirements.This is a hands-on leadership role, working closely with Operations, Engineering, and Customers to ensure robust processes, effective risk management, and audit readiness at all times.Key ResponsibilitiesOwn, maintain, and develop the ISO 13485 Quality Management SystemAct as site lead for external audits (customers, notified bodies, regulators) and internal auditsManage CAPA, deviations, non-conformances, and complaints through to effective closureEnsure compliance with regulatory and customer requirements for medical device manufactureOversee document control, change control, and validation documentationLead quality input into new product introduction (NPI) and process changesManage supplier quality, including supplier approval and performance monitoringDrive continuous improvement and quality culture across the businessProvide leadership and mentoring to quality team members as their line managerSkills & Experience RequiredProven experience as a Quality Manager (or Senior Quality Engineer) in a manufacturing environmentStrong working knowledge of ISO 13485 (medical devices essential)Experience within plastic injection moulding, cleanroom, or medical manufacturing highly desirableConfident leading audits and interfacing with customers and external bodiesPractical experience of CAPA, risk management, and validation activitiesStrong attention to detail with a pragmatic, solutions-focused mindsetExcellent communication skills at all levelsStrong IT skills for working in a data-driven environment (ERP experience desirable)What We OfferKey leadership role within a respected medical manufacturing businessOpportunity to shape and strengthen quality systems and cultureStable, long-term position in a growing and technically capable organisationCompetitive salary, commensurate with experience

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