Quality Compliance Auditor

Almac Group; Craigavon; On-site; GBP 42,000 - 64,000; Full time

Job summary

Almac Group is seeking a Quality Compliance Auditor to support GMP compliance for Drug Substance and Drug Product manufacturing for the UK and Ireland. The role reports to the Clinical Services unit and is based in Craigavon with office-based duties.

You will collaborate with Qualified Persons, ensure timely regulatory submissions, and uphold high quality standards in a fast-paced, regulated environment. After initial six months in-office, hybrid working may be considered under applicable terms.

Qualifications

• Must have a Bachelor's degree in biology, pharmacy, chemistry or related subject.
• Relevant experience in a pharmaceutical manufacturing, laboratory or GMP environment.
• Eligible to work in the UK without restrictions or hold a valid work permit for full-time employment in the UK.

Responsibilities

• Support Almac Clinical Services' Qualified Persons in the UK and Ireland to ensure GMP compliance across Drug Substance and Drug Product manufacture.
• Work to internal timelines and regulatory expectations to maintain high quality standards.
• Contribute to delivering vital medicines to patients by upholding quality and compliance.

Skills

Organisational skills

Problem-solving abilities

Effective communication

Attention to detail

Relationship building

Education

Bachelor's degree in biology/pharmacy/chemistry

Job description

Quality Compliance Auditor

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.

Closing Date

We will no longer be accepting applications after 5pm on 28th October 2026.