Responsibilities
Please make sure you read the following details carefully before making any applications.
* 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
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Skills, Education & Qualifications
* PhD preferred 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