Data and Document Reviewer

OASIS Group; Craigavon; On-site; GBP 32,000 - 46,000; Full time

Benefits offered by this job

Paid Time-Off for Vacation and Sick**

Job summary

Almac Group in Craigavon, Northern Ireland, is seeking a Data and Document Reviewer to join the Analytical Compliance DADR team. You will perform, monitor and own a range of Quality Control data checking and reviewing activities to uphold GMP standards across API manufacturing.

Working in a fast-paced, collaborative environment, you will contribute to the development and manufacture of life-changing medicines with extensive training and clear career progression pathways across the Almac Group.

Qualifications

• 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

Responsibilities

• Perform, monitor and take ownership of a range of Quality Control data checking & reviewing activities
• Ensure the highest standards of quality are maintained across operations
• Contribute to development and manufacture of life-changing medicines

Skills

Analytical Chemistry

Data Review

Quality Compliance

GMP Experience

Education

Analytical/Chemistry degree

Job description

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.

Skills and attributes

• Analytical Chemistry
• Data Review
• Quality Compliance
• GMP Experience

Description

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.

• 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

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

• Paid Time-Off for Vacation and Sick Days

Almac Group is an Equal Opportunity Employer