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Title: Quality Control AnalystLocation: Dartford - Fully on-siteClient: Leading Pharmaceutical CompanyType: 6 months contract - full timeShifts: 3 weeks rotation Early shift 6am - 2pm Monday-FridayLate shift 1:30pm - 10pm Monday-Thursday, 1:30pm - 7pm FridayNight shift 9pm - 7am Scroll down to find an indepth overview of this job, and what is expected of candidates Make an application by clicking on the Apply button.Main ResponsibilitiesImplement and document Musterzge (sampling) of raw materials for the manufacture of clinical trial suppliesPerform and document incoming goods inspections, ensuring compliance with internal and regulatory standardsManage storage, retention, and archiving of samples and all related documentationParticipate in quality-releasing processes for printed labelsConduct quality control of product distribution to ensure compliance and traceabilitySupport the development and optimization of test proceduresPerform analytical testing of in-process controls and composite samples in accordance with GMP and EHS requirementsExecute analyses using defined methods and SOPs within agreed timelinesCarry out a broad range of tests, including Particle size analysis, Cleaning verification, FTIR identification testing etcReview, approve, and report QC data, ensuring accuracy, clarity and compliance with cGMPPrepare test methods for particle size and cleaning verification analysesCompile and issue analytical documentation such as Statements of Results, Certificates of Analysis, and Cleaning CertificatesMain RequirementsCompleted training as PTA, CTA, PCA, MFA, or pharmaceutical ZMFA (or equivalent technical training)Practical experience in quality control of pharmaceuticals and/or packaging materialsStrong command of English, both written and spokenHigh attention to detail, accuracy, and documentation qualityAbility to work independently and efficiently while maintaining compliance with GMP standardsWillingness to work flexible hours, depending on operational needsABOUT PLANET PHARMAPlanet Pharma is an American parented Employment Business/Agency that provides global staffing services with its head-quarters in Chicago and our EMEA regional office located in Central London. We have invested significantly in creating a robust international platform that enables us to work compliantly in 30+ countries with a current network of 2500+ active contractors globally as well as a very strong permanent / direct hire recruitment offering.Our specialist knowledge and close relationships with our clients and the wider industry really makes us unique in our field. Just recently we were recognised by FORBES as the 17th best professional staffing firm, and have won multiple awards from industry accredited bodies for our commitment to excellence and service delivery. We have extensive functional expertise including: Regulatory Affairs, Pharmacovigilance, QA, QC, Submissions experts, Clinical development, Quality, Biostatistics, and Medical Affairs / Writing. xjdpvnf We are an equal opportunities Recruitment Business and Agency.We welcome applications from all suitably qualified candidates regardless of their race, sex, disability, religion/belief, sexual orientation or age.