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An experienced analytical chemist and has extensive method development background producing methods for challenging molecules from scratch to tight deadlines and validating these. He is experienced on HPLC in various modalities, LCMS, GCMS and looking to apply his skill set in a company in Yorkshire/ keen to relocate home.

Seeking a new challenge after working at the same company for many years. Has a broad knowledge of extraction and analytical processing methods across a range of instrumentation, worked in multiple departments across the company as well as liaised with many others. Main skills are in HPLC, UPLC training, GC MS, LC MS and GC FID using various wet chemistry extraction techniques including SPE.

This candidate is is an experienced QA and Validation Manager who has worked recently for a top European Pharmaceutical company concerned with contract development and manufacturing. He has worked on a lot of products here across tablets and injectables, dealing with validation of a rapidly changing landscape of processes in a GMP enrionment. The company is a specialist in manufacture of pharmaceuticals and take in projects to ensure that products are manufactured efficiently in a clean room environment. He had responsbiilities towards preparation of validation protocols, IQ, OQ and PQ and overseeing ‘shop floor’ activties. This involved data collation, coordination with departments, fluid communication and generally any abnomarlities and he gets accross it quickly. He has prepared the validaton master plan and developed standard operation procedures including facility, process and cleaning validations.

Candidate ref 10613 Experienced Synthesis Chemist Senior Scientist in synthetic chemistry, working on pharmaceutical early-to-late stage process development projects. Is seeking the next career step. Has 3 years of experience coupled with their MChem degree, the industrial work has mainly involved using experiments and process analytical techniques to guide the development of processes. Has worked to a high scale of production, up to 50kg and routinely works with jacketed vessels in these synthesis activities. Has proficiency in the use of LC-MS, GC-MS, NMR and other characterisation techniques. To receive a full copy of this candidates CV, please email admn@licasci.com quoting reference 10613

This candidate is experienced in working for two companies both global pharmaceutical. He is seeking a role in analytical chemistry, having a keen interests in LC-MS, HPLC, GC-MS, NMR and FTIR. He would like to find a role ideally in analytical chemistry which can apply his experience as a research chemist. He has experience of working in a GxP environment, working on controlled drugs and reviewing COSHH and risk assessments for potent material. He is experienced in method development, process investigation and compound characterisation.   He holds an MChem and has experience of two roles, one as Analytical Development in a multidisciplinary department using HPLC, LC-MS, GC and GC-MS, the second role has been as a Synthetic Chemist working in API production in a GxP environment using reflux, distillation, separation, recrystallisation and workup.   He is immediately available to interview or start a role, and is seeking this within the North West of the UK.

Experienced Study Director working with Global Pharmaceutical and Medical Device Companies. Experience with varied analytical techniques including; LC-UV-MS (Waters QToF, TQS and QDa systems). DI-GC-MS. NMR. Ability to quickly diagnose and repair instrument faults at both the hardware and software level. A sound understanding of GLP within an Analytical/QC environment. Development and validation to ICH guidelines of UPLC and GC methods for both screening and targeted analysis of trace level components.