Get more replies from employers
Send a job-specific resume in minutes.
Almac Group is seeking a Quality/Analytical Compliance DADR to support the manufacture of Active Pharmaceutical Ingredients in GMP facilities. You will perform data checking and reviewing activities to ensure the highest quality across operations.
Join a fast-paced, collaborative team with opportunities for professional growth and clear career progression pathways across the Almac Group.
37.5 hours per week. Monday – Friday, flexible working hours
HRJOB11822
Almac Sciences
Craigavon, Northern Ireland, UK
Internal and external candidates
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.
Sunday 13th September 2026 at 5pm local time
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