Join our quality team where you will be responsible for providing active ingredients that meet the highest pharmaceutical regulatory and compliance standards. This opportunity is for a Senior QC Analyst Validation to join the QC Technical Services Team on a temporary basis. Your Responsibilities You will: Ensure effective troubleshooting of equipment or technique failures and troubleshooting of problems associated with various analytical techniques. Takes responsibility for promoting and improving technical skills and quality standards within QC. Sample, analyse and release API, drug products, test incoming raw materials and drug packaging, provide import testing for drug product batches, CDMO batch testing, In process samples, cleaning validation, verification analysis and batch release for raw materials. Write, review, and drive the completion of validation/analytical transfer activities, owning your analytical projects within the team. Develop, train and report validation and transfer activities within QC for new and existing clients. Perform effective reactive and proactive investigations, driving continuous improvements. Drive compliance working with QA and promote quality standards. Ensure that departmental objectives are implemented in line with the overall Quality/Corporate goals. Comply with all safety and GMP requirements within the Laboratory. Document all testing activities to regulatory standards. Participate in and facilitate improvement programs within the Laboratory. Ensure that all interactions and engagements are carried out with the highest ethical and professional standards and that all work is accomplished with quality and in accordance with the client’s values. Complete additional tasks considered necessary to meet business and customer requirements as indicated by the team leader. Our Requirements Sciences degree or equivalent in a relevant science subject. Proven pharmaceutical experience handling HPLC, GC FTIR, UV, PXRD, DSC. GMP knowledge coupled with proven experience of analytical method validation & transfer principles. Excellent communication skills. What we offer Competitive hourly rate and retention bonus Training & development Open and friendly work environment Culture & Values We bring our culture to life in the way we work every day. Our culture enables career development and talent management, we recognise that how we do things is as important as what we do, and our values set out how we achieve our goals and help us "do it right". Diversity & Inclusion We are committed to nurturing a culture of diversity and inclusion that contributes to improving innovation, performance, and engagement. We value transparency, mutual respect, and equal treatment of people. For this reason, we are firm in protecting our employees against any forms of discrimination. We are Disability Confident - Committed which means we make reasonable adjustments to our process and offer interviews to disabled people who meet the minimum criteria for our vacancies. If you would like any assistance or require the application to be completed in a different format, please call or contact our Haverhill site reception. Environment, Social and Governance We strongly believe that the success of our company lies in its capacity to adapt to tomorrow’s challenges. Our responsibility as a company is to provide sustainability and resilience to the pharmaceutical value chain. EUROAPI UK Limited (now part of Particle Dynamics) Website : https://particledynamics.com/ Apply Today! Find out more about this exciting opportunity, apply today or contact Marie Meekings.