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Quality Compliance Auditor

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Hybrid

Quality Compliance Auditor

Almac Group

Quality Compliance Auditor

Skills

Talent AcquisitionCompliance

11 days ago

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Important information


Contract type:

Permanent

Location:

Craigavon, UK

Work mode:

Hybrid

Published on:

14 October 2026

What they need


Who We Are Almac Group is a global leader in advancing human health. We provide a range of expert services across the drug development lifecycle to pharmaceutical and biotech companies, supporting them in finding treatments for patients.

Location: Craigavon, Northwest or Dundalk (office based)

Hours: 37.5 hours per week

Business Unit : Clinical Services

Open To : Internal & External Candidates

Ref No.: HRJOB11947

The Opportunity As a Quality Compliance Auditor, you will play an important role in supporting Almac Clinical Services’ Qualified Persons in the UK and Ireland, helping to ensure that every required stage of Drug Substance and Drug Product manufacture meets GMP standards and applicable regulatory submissions. Working to internal timelines and customer and regulatory expectations, you will contribute directly to maintaining the high standards of quality and compliance that support the delivery of vital medicines to patients.

“Joining Almac means becoming part of a fast‑paced, growing organisation within a highly regulated industry. We offer a supportive and collaborative working environment, with excellent opportunities for learning, development and long‑term career progression across the Almac Group. Our approach is simple – we support, develop and reward our people, build fulfilling careers and together we advance human health. More information can be found here; Life at Almac - Almac ” What You Need To Be Successful To be successful in this position, you must either be eligible to work in the UK without restrictions or hold a valid work permit enabling you to undertake full-time employment in the UK.

Additionally, you will need a Bachelor’s degree in biology, pharmacy, chemistry or a related subject (or equivalent) qualification.

Candidates must also have relevant experience in a pharmaceutical manufacturing, laboratory or GMP environment.

For further information on essential and desirable criteria, please review the job description attached to the online job posting.

Skills And Attributes

  • Strong organisational and problem-solving abilities
  • Effective communication skills
  • Microsoft Office Packages (to include Outlook, Word, Excel and PowerPoint)
  • Strong attention to detail
  • Ability to build effective relationships with internal and external stakeholders

Further information Please note this role is not a remote position you will be required to work full time in the office for the first six months and there after a successful probationary you can avail of hybrid working (T&C’s apply).

The role will be based at our Craigavon, Northwest or Dundalk facility, depending on the successful candidate’s location.

How To Apply Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible. Closing Date We will no longer be accepting applications after 5pm on 28th October 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.

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