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Quality Assurance Manager - Project Lead

Consult
Posted 14 days ago, valid for a month
Location

Nottingham, Nottinghamshire NG42QU, England

Salary

£40,000 - £60,000 per annum

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Contract type

Full Time

Life Insurance

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.

Sonic Summary

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  • Salary: Negotiable dependent on experience plus benefits
  • Year of Experience Required: Seasoned QA professional
  • Contract: Until end of Dec 2024 (3 days a week)
  • Responsibilities:
    • Oversee operational activities from a QA perspective
    • Provide leadership and mentorship
    • Manage change controls, deviations, CAPAs
    • Review and approve operational documents
    • Stay up-to-date on pharmaceutical regulations
  • About You:
    • Seasoned QA professional with sterile manufacturing experience
    • Proven leader with management background in QA
    • Skilled communicator with attention to detail
    • Prior experience with managing change controls and validation processes

Contract until end of Dec 2024 (3 days a week)

Salary Negotiable dependent on experience plus benefits

Scope

My client are an expanding pharmaceutical manufacturing organisation seeking a highly motivated and experienced Quality Assurance Manager to join their sterile manufacturing facility. This project lead role offers the opportunity to make a significant impact to their dynamic and growing company with a focus on quality and continuous improvement. This will be on an initial fixed term contract on 3 days a week, until the end of 2024 with scope to continue into 2025.

Responsibilities

  • Oversee all operational activities from a QA perspective, ensuring compliance with GMP and regulatory requirements.
  • Provide leadership and mentorship to the team, fostering a strong understanding of good manufacturing practices (GMP).
  • Conduct regular self-inspections and facilitate continuous improvement initiatives.
  • Manage change controls, deviations, CAPAs, and qualification documentation.
  • Review and approve operational documents within the Quality Management System.
  • Partner with internal stakeholders to provide expert QA guidance.
  • Stay up-to-date on current and evolving pharmaceutical regulations.

About You

  • A seasoned QA professional with experience in pharmaceutical manufacturing from sterile environments (aseptic/terminal sterilization both considered).
  • A proven leader with a management background in Quality Assurance.
  • A skilled communicator with the ability to influence, troubleshoot, and work effectively within a team.
  • An individual with meticulous attention to detail, strong planning and organizational skills, and the ability to thrive under pressure.
  • Prior experience with managing change controls, technical protocols, validation/qualification processes, and batch record reviews.

If you're interested in the above role then please click apply or get in touch to discuss further.

Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.

Benefits:

  • Company pension
  • Life insurance
  • On-site parking
  • Private medical insurance

Schedule:

  • Flexitime
  • Monday to Friday

Apply now in a few quick clicks

In order to submit this application, a Reed account will be created for you. As such, in addition to applying for this job, you will be signed up to all Reed’s services as part of the process. By submitting this application, you agree to Reed’s Terms and Conditions and acknowledge that your personal data will be transferred to Reed and processed by them in accordance with their Privacy Policy.