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Adherence to all Good Manufacturing Practices (GMP) Safety StandardsJob Description
Thermo Fishers clinical research business is a leading global contract research organization and world leader in serving science. We are passionate deliberate and driven by our mission to enable our clients to make the world healthier safer and cleaner.
Within our Analytical Services team we have a functional service provider solution which is an outstanding partnership that allows our customers to use the experience of our staff while allowing you the employee to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company all while maintaining full-time benefits.
Summarized purpose:
We are currently recruiting an Analytical Scientist to be based within out client site in Stevenage Hertfordshire UK. This role will see you performing analysis and running analytical methods principally using solid-state NMR spectroscopy but also solution NMR spectroscopy for GMP and non-GMP testing of drug substances and drug products being developed as new medicines.
The successful candidate will be involved with a diverse range of activities including:
Performing analytical testing particularly using NMR spectroscopy (primarily solid-state NMR) of drug substance and drug product using established and investigational analytical methods.
Preparation and management of samples (powder tablets etc) and instruments for NMR analysis.
Performing and managing calibration/maintenance tests of solid-state NMR instruments.
Owning and managing analytical testing through the lifecycle from early phase product development to marketing.
Supporting the development of new analytical methods for testing drug substance and drug product during product development
Collaborating closely with analytical colleagues in Stevenage and in our partner team in Philadelphia as well as colleagues in chemistry formulation and manufacturing teams
Owning and managing interactions with third parties (contractors suppliers testing laboratories academic and industry groups) e.g. communication data/information flow shipment of materials etc.
Expected Qualifications:
BSc in chemistry biochemistry pharmaceuticals or related scientific discipline
Strong organisational skills and ability to work across multiple projects in parallel
Excellent interpersonal communication skills
Demonstrated excellence in technical writing skills
Demonstrable ability to work in multi-disciplinary multi-cultural teams
Demonstrable ability to work independently and influence others
Demonstrated ability to work to high standards of quality and safety
Preferred Qualifications:
Experience in analytical method development/validation for pharmaceutical biopharmaceutical products
Experience in regulated GxP laboratory working including an understanding or experience of method validation requirements
Knowledge and understanding of Digital Data and Analytics principles tools and approaches and ideally experience of utilising such tools and workflows
Experience and interest in NMR spectroscopy
Our 4i Values:
Integrity Innovation Intensity Involvement
If you resonate with our 4i values above and ultimately wish to accelerate the delivery of safe and effective therapeutics for some of the worlds most urgent health needs submit your application wed love to hear from you
Full-Time