Join to apply for the Quality Assurance Specialist role at Almac Group

Join to apply for the Quality Assurance Specialist role at Almac Group

The Role

The role focuses on ensuring and enhancing the quality and GMP (Good Manufacturing Practice) compliance of pharmaceutical products within Almac Pharma Services.

(9 – 12 month Fixed Term Roles)

Location: Craigavon

Hours: 37.5 hours per week

Salary: Competitive

Business Unit: Pharma Services

Open To: Internal & External Applicants

Ref No.: HRJOB10874

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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 areas—including manufacturing, quality control, product development, and distribution—to 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

• 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 (or equivalent) in a Life Science or closely related field OR Significant experience working within the Pharmaceutical Industry along with demonstrable knowledge may be considered as sufficient to meet educational requirements for this role.
• Significant experience working within an established Quality System (e.g. GMP, ISO)
• Comprehensive, working knowledge of the regulatory requirements for pharmaceutical products are essential, including familiarity with the principles of Good Manufacturing Practice, Pharmaceutical Quality Systems, Quality Risk Management and Pharmaceutical Product Lifecycles
  
  

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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