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QA Manager

SRG
Posted a day ago, valid for 12 days
Location

Port Talbot, West Glamorgan SA13 1NR, Wales

Salary

£42,000 - £50,400 per annum

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Contract type

Full Time

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Sonic Summary

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  • The job title is QA Manager for a manufacturing organization located in South Wales.
  • Candidates should have extensive experience in GMP life science manufacturing, preferably in a pharmaceutical setting, with at least 5 years of relevant experience.
  • The role involves overseeing a QA team, developing and implementing the company's Quality Management System (QMS), and ensuring compliance with regulatory standards.
  • A qualification in a scientific or engineering field is required, along with strong communication skills and experience with regulatory bodies like the MHRA or FDA.
  • The salary for this position is competitive, reflecting the candidate's experience and qualifications.

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Job title: QA Manager

Are you a lead or manager within the Quality, Quality Assurance, or Quality Management System experience within a highly regulated environment? An opportunity has arisen for a QA Manager to join a manufacturing organisation based in South Wales.

About the Job:

We require a QA Manager with extensive experience in GMP life science manufacturing, ideally within a pharmaceutical environment, with exposure to drug manufacturing, aseptic filling, packaging or site services equipment, with interest in working within a highly regulated production environment.

In this role you will work interdepartmental as the QA SME, promoting a strong GMP culture within a small team of QA Officers, with aims of fostering an attitude of strong continuous improvement and audit readiness.

Summarised responsibilities:

  • Overseeing the QA team, reporting into head of department, and leading cross-functional QA activities to deliver on quality objectives
  • Developing and implementing the companies QMS in accordance with ISO 9001, ICH Q10, ensuring compliance is in line with UK Human Medicines Regulations, the Orange Guide, and EudraLex.
  • Carrying out risk assessments, conducting audits (internal & external), SOP's, work instructions, and forms or records.
  • Showcasing excellent communication skills when dealing with regulatory bodies, external suppliers, and reporting up to head of department and director
  • Promoting a continuous improvement culture ensuring audit readiness through cross functional departments
  • Showcasing confidence to make suggestions and challenge new ways of doing things to support a new and growing team

About you:

  • Qualification in Science (Chemistry, Pharmacy, Biology etc), Engineering, or equivalent Manufacturing experience
  • Strong Quality Assurance experience within a GMP environment
  • Proficiency in Quality Management Systems, ideally PQS
  • Experience dealing with the MHRA, FDA, or EMA
  • Previous lead or management experience
  • Positive can-do attitude with drive to lead continuous improvement
  • Good communication skills

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.

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