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Join to apply for the Quality Assurance Associate role at Almac Group
The Role
The QA Associate will focus on ensuring compliance with Good Manufacturing Practice (GMP) and internal procedures through meticulous review of documentation and data. The post holder will review GMP documentation such as executed batch documents, liaising with relevant personnel to resolve discrepancies and ensure accuracy. Review of shipping paperwork from Almac depots, and review and approval of Packaging Specifications on behalf of the customer is also a key responsibility.
Location: Craigavon
Hours: 37.5 hours per week
Salary: Competitive
Business Unit: Clinical Services
Open To: Internal & External Applicants
Ref No.: HRJOB10680
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The Role
The QA Associate will focus on ensuring compliance with Good Manufacturing Practice (GMP) and internal procedures through meticulous review of documentation and data. The post holder will review GMP documentation such as executed batch documents, liaising with relevant personnel to resolve discrepancies and ensure accuracy. Review of shipping paperwork from Almac depots, and review and approval of Packaging Specifications on behalf of the customer is also a key responsibility.
You will also support continuous improvement by identifying trends and proposing process enhancements, while maintaining detailed records of reviewed documentation to aid resource planning. A key aspect of the role involves providing timely and accurate responses to customer queries and supporting the QA ServiceDesk with documentation approvals and system tasks.
The role requires a proactive approach to quality assurance, with an emphasis on customer focus, compliance, and continuous improvement.
Full details of the job role can be found in the Job Description attached at the bottom of this job advert.
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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
* Degree level qualification (or equivalent)
OR
* 3x A-Levels (or equivalent) AND previous significant experience gained from working within Almac Clinical Services Quality
Please note further desirable criteria contained within the Job Description attached at the bottom of the job advert.
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Further Information
The working pattern for this role is based on a flexi Evening shift between the hours of 14:30 – 01:00 with the following core hours:
* Monday – Thursday 16:30 – 23:30
* Friday: 16:30 – 23:00
You must work 37.5 hours per week.
During periods of high-volume work requests this role will require additional coverage beyond normal working hours and it is a condition of your employment that you are able to fulfil this requirement of the role.
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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 25 Jun 2025
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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