Contact Heather Lennox | | Data Analyst (Pharmaceutical) - Coleraine - PermanentAre you detail-driven with a passion for quality and compliance? Were 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:Enhanced annual leave entitlementHealthcare and wellbeing initiativesPension schemeLife assuranceTraining and career development opportunitiesEmployee assistance programmeModern working environmentHealth & wellbeing activitiesRecognition and reward initiativesThe RoleWorking 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.Reviewing analytical data for products, materials, validation, and stability studiesReviewing equipment calibration and verification recordsCompiling and reviewing laboratory testing instructions, specifications, and SOPsPreparing validation protocols and reviewing associated reportsCoordinating calibration schedules for laboratory equipmentPreparing and reviewing technical reports and regulatory submission documentationSupporting qualification activities for facilities and equipment when requiredMaintaining compliance with cGMP, FDA, MHRA, and internal quality standardsSupporting a safe working environment through adherence to EHS procedures and participation in inspections and risk assessmentsWorking flexibly to support departmental and business objectivesCriteria:Degree in Chemistry or a related scientific disciplineExperience working within a GLP/GMP regulated environmentKnowledge of pharmaceutical regulatory requirements, particularly FDA or MHRA standardsStrong attention to detail and organisational skillsComfortable working independently and collaboratively within strict regulatory frameworksProficient in Microsoft Office and computer-based systemsSelf-motivated with a proactive approach to problem solvingIf this sounds like the next step in your career, wed love to hear from you! Even if you dont meet every listed requirement, we encourage you to apply we may have other suitable roles for you. Apply online, email or call Heather on to find out more.Riada Resourcing is an equal opportunities employer.Skills:Admin AnalystWHJS1_NI