Role Overview
The role focuses on ensuring and enhancing quality and GMP compliance of pharmaceutical products within Almac Pharma Services. The post holder will be responsible for monitoring and reviewing operational areas—manufacturing, quality control, product development and distribution—to assess and maintain regulatory compliance. They will provide quality assurance support across departments, collaborate with internal and external stakeholders, and help meet project timelines.
In addition, the post holder will contribute to the development and continuous improvement of quality systems, including deviation management, CAPA, change control and risk assessments; participate in audits; review critical documentation; support supplier processes; review production and laboratory data; compile product quality reviews; and serve as the key contact for compliance queries, safeguarding product quality.
Location
Craigavon
Working Hours
37.5 hours per week. Flex pattern 07:00–19:00 with core hours 10:00–16:00. Coverage beyond normal hours is required. Hybrid working available after probation.
Remuneration
Competitive salary.
Business Unit
Pharma Services.
Applicants
Open to internal and external applicants.
Eligibility & Requirements
* Eligibility to work in the UK or a valid UK work permit.
* Degree (or equivalent) in Life Science or closely related field, or significant industry experience with demonstrable knowledge.
* Significant experience within an established quality system (e.g., GMP, ISO).
* Comprehensive working knowledge of regulatory requirements for pharmaceutical products: Good Manufacturing Practice, Pharmaceutical Quality Systems, Quality Risk Management, and Product Life Cycles.
Reference Number
HRJOB11469
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