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Almac Group

Quality Assurance Specialist (9-12 Month Contract)

Craigavon
Posted 1 day ago
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Quality Assurance Specialist (9-12 Month Contract)

Role: Quality Assurance Specialist – GMP Compliance (Fixed Term Contract)

Location: Craigavon Contract: 9-12 Month Fixed Term Contract Hours: 37.5 hours per week Salary: Competitive Business Unit: Pharma Services Open To: Internal & External Applicants Reference No.: HRJOB11609


The Role

The Quality Assurance Specialist (GMP Compliance) plays a critical role in ensuring the quality and regulatory compliance of pharmaceutical products within Almac Pharma Services.

Key Responsibilities

  • Monitor and review operational areas, including manufacturing, quality control, product development, and distribution, to assess and maintain compliance with regulatory standards.
  • Provide expert quality assurance support across departments and collaborate with internal/external stakeholders to uphold product integrity and meet project timelines.
  • Develop and continuously improve quality systems, including:
    • Deviation management
    • CAPA (Corrective and Preventive Action)
    • Change control
    • Risk assessments
  • Participate in internal and external audits, review critical documentation, and support supplier management processes.
  • Analyse production and laboratory data, compile product quality reviews, and act as a key contact for compliance-related queries to ensure safety and regulatory excellence of pharmaceutical products.

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Key Requirements

  • Eligibility to work in the UK OR a valid work permit permitting full-time employment.
  • Degree (or equivalent) in Life Science or a closely related field OR substantial experience within the pharmaceutical industry (equivalent knowledge may be accepted).
  • Significant experience in an established quality system (e.g., GMP, ISO).
  • In-depth knowledge of regulatory requirements for pharmaceutical products, including:
    • Good Manufacturing Practice (GMP)
    • Pharmaceutical Quality Systems
    • Quality Risk Management
    • Pharmaceutical Product Lifecycle Management

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Further Information

  • Working Pattern: Flexible hours (07:00–19:00), with core hours (10:00–16:00).
  • Availability: Regular coverage required beyond normal working hours—essential for this role.

Apply Online: Tailor your CV to demonstrate how you meet this role’s criteria. Upload your resume in PDF format. Applications close at 5:00 PM on 10 July 2026.


Recruitment Agencies: Only applications submitted through invited Talent Acquisition partners will be considered. Unsolicited CVs will not qualify for a fee. Thank you.

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Skills

Quality Assurance
GMP
Regulatory Compliance
Pharmaceutical Products
Quality Systems
Deviation Management
CAPA
Change Control
Risk Assessments
Internal Audits
External Audits
Documentation Review
Supplier Management
Data Review
Product Quality Reviews

Location

Craigavon, Northern Ireland, United Kingdom

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