Product Quality Auditor

Almac Group; Craigavon; On-site; GBP 38,000 - 50,000; Full time

Job summary

Almac Group seeks a Product Quality Auditor to join the Pharma Services team in Craigavon. The role entails reviewing batch records before QP certification and release, ensuring batch compliance and timely release to meet KPI targets and customer promises.

The successful candidate will work on-site at the Craigavon headquarters, supporting continuous quality objectives within a busy production environment and contributing to KPIs and quality system improvements.

Qualifications

• Minimum five GCSEs (incl. English and Maths) and three A Levels.
• Significant experience working within a GMP/ISO quality system.
• Experience reviewing batch records and performing QA audits.

Responsibilities

• Review batch records prior to QP certification and release to ensure compliance.
• Support KPI data generation and ensure on-time batch release in line with OTIF timelines.

Skills

Batch records

GMP/ISO experience

Audit/inspection

Education

GCSEs & A-levels

Job description

Location: Craigavon

Hours: 37.5 Hours (Full time on-site)

Salary: Competitive

Business Unit: Pharma Services

Open To: Internal & External Applicants

Ref No.: HRJOB12018

The Role

Working as part of the Pharma Services Business Unit, based in our Headquarters in Craigavon, the Product Quality Auditor will work as part of the Product Quality Team responsible for review of batch records prior to QP certification and release. They will support the Product Quality department objectives in relation to the delivery of batches in line with OTIF timelines, including performing the associated electronic transactions required to generate KPI data. They will also ensure customer requirements for batch release are met in relation to Promise Date, elevate any anticipated issues in meeting these timelines to the Product Quality Team Leader and log constraints as required. As part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group. For a full list of job specific responsibilities please see attached Job Description.

Essential Criteria

• 5 GCSEs (or equivalent) at Grade C or above including English Language and Maths
• 3 'A' Levels
• Previous significant experience working within an established Quality System (e.g. GMP, ISO)

Desirable Criteria

• Level 5 qualification or above
• Previous experience in review/auditing of GMP records
• Previous experience working within a production environment
• Previous experience working within a pharmaceutical manufacturing environment

**Please note that if you have applied for this role within the past 6 months your interview score will remain valid and you do not need to reapply**

Closing Date

We will no longer be accepting applications after 5pm on Wednesday 11th November 2026

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 CV's received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.