| Position | Quality Assurance Specialist |
| Posted | 26 Jul 2026 |
| Expired | 25 Aug 2026 |
| Company | Almac Group Ltd |
| Location | Craigavon | GB |
| Job Type | Full Time |
Latest job information from Almac Group Ltd for the position of Quality Assurance Specialist. If the Quality Assurance Specialist vacancy in Craigavon matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.
Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Almac Group Ltd for the position of Quality Assurance Specialist below matches your qualifications.
Location: Craigavon
Hours: 37.5 hours per week
Salary: Competitive
Business Unit: Pharma Services
Open To: Internal & External Applicants
Ref No.: HRJOB11720
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The Role
The role focuses on ensuring and enhancing the quality and GMP (Good Manufacturing Practice) compliance of pharmaceutical products within Almac Pharma Services.
The post holder will be responsible for monitoring and reviewing various operational areasincluding manufacturing, quality control, product development, and distributionto assess and maintain compliance with regulatory standards. They will provide expert quality assurance support across departments, collaborating with internal and external stakeholders to uphold product integrity and meet project timelines.
In addition to oversight responsibilities, the post holder will actively contribute to the development and continuous improvement of quality systems such as deviation management, CAPA, change control, and risk assessments. They will participate in internal and external audits, review critical documentation, and support supplier management processes.
The role also involves reviewing production and laboratory data, compiling product quality reviews, and serving as a key contact for compliance-related queries, all with the overarching goal of safeguarding the quality and regulatory compliance of pharmaceutical products.
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Key Requirements
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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.
You will be eligible for hybrid working following the successful completion of probation.
This role requires coverage beyond normal working hours on a regular basis 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 7th August 2026
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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 CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.
Skills:
Quality System Knowledge of GMP Pharmaceutical Manufacturing
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