Quality Compliance Team Leader

Quality Compliance Team Leader

Location: Craigavon, Northern Ireland, UK

Hours: 37.5 per week, Mon-Fri with flexible working hours

Business Unit: Almac Sciences

Open To: Internal & External Applicants

Ref No.: HRJOB11539

The Opportunity

The post holder will lead a team of Quality Compliance professionals supporting manufacturing operations, ensuring timely delivery of GMP project support. The Quality Compliance Team Leader is responsible for QA approval and release of GMP products in line with internal procedures, while working closely with the wider quality function to maintain robust, compliant Quality Management Systems.

A strong focus on coaching and mentoring will ensure team capability, performance, and continuous development.

Join Almac Sciences and be at the forefront of life-changing innovations. This is your chance to contribute to cutting-edge pharmaceutical solutions whilst advancing your own career in a supportive, forward-thinking environment.

For further information on candidate criteria and job specific responsibilities, please review the attached Job Description.

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

Key Requirements

· Life Sciences Degree level qualification

· Significant Experience of QA/Compliance within a Pharmaceutical GMP environment.

· Significant Experience of reviewing manufacturing documentation such as batch records and analytical data

· Significant Experience of investigation of Analytical and Manufacturing deviations

Desirable Requirements

· Prior QA Manufacturing Support Experience Gained in a GMP API Company (CDMO or CRO) working to ICHQ7.

· Experience of preparation for regulatory audits (MHRA, FDA)

· Previous experience of supervising a team / leading a team

Apply Now:

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 Wednesday 27th May 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 CVs received or submitted directly to Hiring Managers will be considered unsolicited and no fee will be payable. Thank you for your cooperation.