Join to apply for the Product Quality Auditor role at Almac Group
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Join to apply for the Product Quality Auditor role at Almac Group
The Role
The role focuses on ensuring pharmaceutical manufacturing and packaging batch records meet Good Manufacturing Practice (GMP) standards. The primary responsibility involves reviewing batch documentation for both commercial and clinical operations, preparing disposition packs for Qualified Person (QP) certification, and assessing any deviations or changes that could impact compliance. The post holder plays a key role in supporting timely batch release by aligning with On Time In Full (OTIF) delivery targets and managing electronic transactions to generate performance data.
Location: Craigavon
Hours: 37.5 hours per week
Salary: Competitive
Business Unit: Pharma Services
Open To: Internal & External Applicants
Ref No.: HRJOB10882
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The Role
The role focuses on ensuring pharmaceutical manufacturing and packaging batch records meet Good Manufacturing Practice (GMP) standards. The primary responsibility involves reviewing batch documentation for both commercial and clinical operations, preparing disposition packs for Qualified Person (QP) certification, and assessing any deviations or changes that could impact compliance. The post holder plays a key role in supporting timely batch release by aligning with On Time In Full (OTIF) delivery targets and managing electronic transactions to generate performance data.
In addition to core responsibilities, the role requires effective communication with internal and external stakeholders, ensuring queries are addressed professionally and promptly. The position also involves verifying data accuracy, supporting continuous improvement initiatives, and performing administrative tasks as needed. Overall, the role is integral to maintaining product quality and regulatory compliance throughout the batch release process.
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Key Requirements
* Have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time employment in the UK
* 5 GCSE’s (or Equiv.) at grade C or above including English & Maths
* 3 A-Levels (or equiv.)
* Previous experience working within an established Quality System (e.g. GMP, ISO)
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Further Information
The working pattern for this role is a flex pattern between the hours of 07:00 – 19:00 with core hours of 10:00 – 16:00.
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Apply Now
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.
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Closing Date
We will no longer be accepting applications after 5pm on 09 Sept 2025
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RECRUITMENT AGENCIES PLEASE NOTE: Almac will only accept applications from agencies/business partners that have been invited to work on this role by our Talent Acquisition team. Speculative candidate CV’s received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Seniority level
* Seniority level
Entry level
Employment type
* Employment type
Full-time
Job function
* Job function
Quality Assurance
* Industries
Pharmaceutical Manufacturing
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