Position: Mid-Senior level

Job type: Volunteer

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Job content

This role is offered as a 12 month fixed-term contract

This will a highly varied role, with exposure to the full range of quality duties associated with pharmaceutical manufacture.

You will be working with a small, friendly team, providing support to teams across our site.

Your role

Working within the Quality department, you’ll be an advocate for embedding a ‘culture of quality’ across Vectura. You’ll provide quality systems expertise to facilitate maintenance and continual improvement of Vectura’s QMS.

Other key responsibilities will include (but not limited to):

  • Maintain the existing quality system by completing a range of tasks across the QMS; e.g. supplier approval.
  • Generate, review and maintain all relevant Quality documentation required by GMP/ISO
  • Identify and implement improvements to the QMS
  • Provide Quality support to project teams and business functions
  • Actively support a continuous improvement culture
  • Perform internal and external audits, and act as subject matter expert for client and regulatory audits
  • Maintain a broad awareness of GMP/ISO requirements, and a detailed knowledge of those pertinent to areas of specialism
  • Lead continuous improvement activities and internal Quality projects as required
  • Provide formal induction and refresher training to individuals across our business

About you

You’ll be educated to bachelor degree standard in a scientific discipline, with experience in a pharmaceutical environment and an understanding of applicable GMP/ISO requirements. You’ll be IT literate with good working knowledge of MS Office applications.

Apply

If you’re looking for a quality role with breadth and variety then we’d love to hear from you. To find out more about the role, Vectura and to apply online, click on the Apply button.

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Deadline: 21-06-2024

Click to apply for free candidate

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