Job Description
Data Analyst (Pharmaceutical) - Coleraine - Permanent Are you detail-driven with a passion for quality and compliance? We’re recruiting for a Data Reviewer to join a leading pharmaceutical manufacturing environment where precision, collaboration, and continuous improvement are at the heart of everything they do.
This is an excellent opportunity for someone with laboratory or pharmaceutical quality experience who enjoys working in a highly regulated environment and wants to be part of a business known for innovation, employee wellbeing and career development. Why apply?
Alongside a competitive, negotiable salary, employees benefit from a strong package designed to support both professional growth and personal wellbeing, including:
1. Enhanced annual leave entitlement
2. Healthcare and wellbeing initiatives
3. Pension scheme
4. Life assurance
5. Training and career development opportunities
6. Employee assistance programme
7. Modern working environment
8. Health & wellbeing activities
9. Recognition and reward initiatives
The Role
10. Working within the Quality Control Laboratory, you will play a key role in ensuring all laboratory data, testing, and documentation meet strict regulatory and GMP standards.
11. Reviewing analytical data for products, materials, validation, and stability studies
12. Reviewing equipment calibration and verification records
13. Compiling and reviewing laboratory testing instructions, specifications, and SOPs
14. Preparing validation protocols and reviewing associated reports
15. Coordinating calibration schedules for laboratory equipment
16. Preparing and reviewing technical reports and regulatory submission documentation
17. Supporting qualification activities for facilities and equipment when required
18. Maintaining compliance with cGMP, FDA, MHRA, and internal quality standards
19. Supporting a safe working environment through adherence to EHS procedures and participation in inspections and risk assessments
20. Working flexibly to support departmental and business objectives
Criteria:
21. Degree in Chemistry or a related scientific discipline
22. Experience working within a GLP/GMP regulated environment
23. Knowledge of pharmaceutical regulatory requirements, particularly FDA or MHRA standards
24. Strong attention to detail and organisational skills
25. Comfortable working independently and collaboratively within strict regulatory frameworks
26. Proficient in Microsoft Office and computer-based systems
27. Self-motivated with a proactive approach to problem solving
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