Data and Document Reviewer
Hours: 37.5 hours per week. Monday Friday, flexible working hours
Ref No: HRJOB11822
Business Unit: Almac Sciences
Location: Craigavon, Northern Ireland, UK
Open To: Internal and external candidates
The Role
Are you passionate about quality, compliance, and delivering excellence in pharmaceutical manufacturing?
Join Almac Sciences and play a key role in supporting the manufacture of Active Pharmaceutical Ingredients (APIs) within our GMP manufacturing facilities. As part of our Analytical Compliance DADR team, you will perform, monitor, and take ownership of a range of Quality Control data checking & reviewing activities, ensuring the highest standards of quality are maintained across our operations.
Working within a fast-paced and innovative environment, you'll be part of a collaborative team contributing to the development and manufacture of life-changing medicines. In return, you'll benefit from excellent opportunities for personal and professional growth, supported by the extensive training, development, and career progression pathways available across the Almac Group.
We will consider applications for either DADR or Senior DADR level. Please review attached Job Descriptions outlining key differences.
Essential Criteria
- Degree level qualification in an Analytical/Chemistry related discipline*
- Previous laboratory experience in a GxP environment
- Working knowledge of multiple laboratory techniques and data review
- A Higher-Level Qualification in relevant discipline, including significant industry experience, may be considered in Lieu of Degree Qualification
Closing Date: Sunday 13th September 2026 at 5pm local time
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
