QC Officers

Marketplace Technical

View: 101

Update day: 07-05-2024

Location: Runcorn North West

Category: Pharmaceutical / Chemical / Biotech

Industry:

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Job content

Leading international Pharmaceutical Manufacturer seeks experienced QC Release Officers.

About the role:

Reporting to a Quality Control Shift Team Leader, you will be performing duties to comply with the quality system in accordance with GMP standards. This role will be a full-time role, based in Runcorn.

Duties may include:

  • Reviewing all pertinent batch documentation as part of the product release process, in order to assess whether a product is compliant with a given specification
  • Approving individual batches for release to market or further internal use,
  • Supporting investigations of non-conformities that may impact upon the release process, product quality or compliance of the facility
  • Contributing to the continuous improvement of all aspects of the quality system to ensure departmental objectives are met and compliance with regulatory requirements is consistently achieved
  • Compiling Certificates of Conformance as required to fulfil company responsibilities to its customers
  • Operating the Quality Assurance databases to support QA in publishing appropriate trends within the business
  • Interfacing with other departments including attendance at meetings to ensure that the requirements of the QMS are met
  • Conducting additional duties as required to support colleagues in the effective execution of their duties
  • Ensuring outsourced products are processed in a timely manner and made available for use with transactions performed on SAP

Skills and experience:

  • Degree in a life science subject or appropriate experience of working in a quality assurance or control related function within either the pharmaceutical/ healthcare related industry
  • Experience of aseptic operations is necessary; if possible aided by experience in aseptic compounding activities
  • Very good knowledge of GMP requirements specifically for manufacturing and control of aseptically produced products as laid down in the Orange Guide
  • Attention to detail
  • A demonstrable ability to communicate effectively
  • IT literate, including Microsoft Office

Apply now for more information

Job Type: Permanent

Schedule:

  • 8 hour shift

Experience:

  • Quality Control: 1 year (preferred)
  • GMP: 1 year (preferred)
  • QMS: 1 year (preferred)

Work authorisation:

  • United Kingdom (required)

Work Location: In person

Reference ID: MATECBB936

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Deadline: 21-06-2024

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