Description Responsibilities · Working in a multidisciplinary team in a GMP environment, performing routine and non-routine analysis of samples such as raw materials, excipients, APIs, drug products and other types of samples · Preparing reagents and solutions for use in analysis · Performing analytical testing of samples using chromatography and other wet chemistry techniques · Development and validation of analytical methods that are appropriate for the requirements of the individual project, under supervision. · Supporting the team by undertaking training and performing projects in physical properties and materials characterisation areas using techniques such as laser diffraction, PXRD, microscopy, thermal analysis etc. · Following scientific methods, protocols, SOPs and Pharmacopoeia accurately and independently · Providing high quality, right first-time, scientifically sound reports and CofAs to clients, meeting their deadlines · Processing and interpreting data, performing calculations, drawing conclusions and reporting, highlighting aberrant or suspect results, and working with supervisor to investigate · Presenting results verbally and in writing, both internally and externally, in a professional manner · Maintenance and troubleshooting of analytical instruments, and solving challenging problems either independently or with assistance from senior personnel · Performing experiments and documentation in accordance SOPs, data integrity and good documentation practices, and Good Manufacturing Practice (GMP) principles · Raising and reporting any OOS and deviations, assisting with investigations and CAPAs, and contributing to laboratory audits as required · Keeping up-to-date with any technological and methodological advancements to support future projects and increase lab capabilities · Organising and managing multiple projects simultaneously if required, working in a flexible manner and able to switch priorities at short notice · Sharing knowledge and expertise to foster a collaborative environment · Skills, Education & Qualifications · A BSc or higher in a relevant scientific field (such as Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Forensics), or substantial practical work experience · A minimum of one year relevant experience of analysis in a pharmaceutical testing laboratory, or equivalent · Working knowledge of a wide range of techniques such as HPLC/UPLC, laser diffraction, microscopy, thermal analysis, PXRD etc. · A strong foundation of basic principles of chemistry and separation science is essential · Experience in method development and validation is desirable but not required · A strong understanding of the pharmaceutical development process and the industry would be advantageous · Experience with Empower, OpenLAB, ChemStation or similar software · Knowledge or experience of working within GxP regulations · Excellent attention to detail and ability to spot inconsistencies