Overview

Contract Length : 9 months (with potential to extend)Pay Rate : £21.92 per hourRole Purpose and ScopeAs a member of the QA Operations Documentation Control Team, your primary responsibility will be to perform Batch Consolidation (auditing) for QC Biochemistry and Microbiology testing activities related to Drug Product (DP) and Drug Substance (DS). You will ensure all QC testing activities are complete and meet release specifications. You will also proactively issue GMP documents and labels to Manufacturing in line with schedules and timelines.Key ResponsibilitiesCoordinate and perform batch consolidation for QC Biochemistry and Microbiology testing.Ensure all testing activities are complete and meet release specifications.Issue GMP documents and labels to Manufacturing, ensuring accuracy and timeliness.Liaise with internal departments to gather required information and maintain effective communication.Support QA Operations in continuous improvement of quality systems and processes.Assist in audit preparation and provide documentation during audits.Lead and manage quality records (Deviations, CAPAs, Change Controls, Investigations).Author, review, and approve GMP documentation.Maintain the archiving system and coordinate document retrieval.Ensure training compliance and maintain an up-to-date training profile.Prioritise workload to meet strict deadlines and support Manufacturing needs.Perform other duties as assigned.Technical and Interpersonal SkillsStrong attention to detail and accurate data entryProficiency in MS Office (Word, Excel, Outlook, Access)Familiarity with database systemsEffective verbal and written communicationRisk-based decision-makingAbility to prioritise workload and meet deadlinesStrong organisational and planning skillsExperience with PQS (Pharmaceutical Quality Systems) is desirableCore CompetenciesAgilityLearns from experience, adapts to change, and embraces new challengesBusiness AcumenUnderstands how their role contributes to business successShares knowledge, listens actively, and respects othersCustomer FocusUnderstands and responds to internal/external customer needsDriving ResultsDelivers high-quality work on time, monitors KPIs, and overcomes challengesLeadershipTakes responsibility, seeks feedback, and contributes to a positive work environmentQualificationsEducation: BSc in Biology or a related field (or equivalent experience)Experience: Entry-level (0–4 years); prior QA/GMP experience is beneficial but not essentialSeniority level

AssociateEmployment type

ContractJob function

Quality AssuranceIndustries: Pharmaceutical Manufacturing

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