Bio-Techne is a world-leading developer and manufacturer of high-quality biological reagents and is seeking a Quality Control Analyst to join their growing team in Bristol.
The successful candidate will join a vibrant and dynamic team of Analysts working on QC analysis for Tocris (a Bio-Techne Brand), testing the products of complex syntheses of biologically active library compounds and novel custom synthesis work for both internal research initiatives and external clients.

EXPERIENCE AND QUALIFICATIONS

• Degree level in Chemistry or related science
• Cultural fit is as important as experience, so we are happy to accept less experience, but QC experience of 3 years plus is desirable (experience in a GMP environment would also be advantageous)
• Detailed knowledge of analytical chemistry with particular expertise in HPLC (and other chromatographic techniques)
• Practical ability and analytical data interpretation skills
• IT skills and competency with Microsoft software packages
• Safe and responsible working manner in laboratory areas

• To carry out QC tests and perform second person checking of other work subject to experience and training. Techniques to include: HPLC, GC, SFC, MS, NMR, FT-IR, UV/Vis, Fluorescence, Melting point, Karl Fischer, Optical Rotation and Solubility.
• To work within and promote our safe working practices, abiding by the COSHH regulations and maintaining a high level of tidiness.
• To be familiar and competent in all required QC and analytical techniques through on the job training and external courses where appropriate.
• Perform method development and validation when required.
• Write and amend standard operating procedures, test methods, specifications and other documents as required.
• Carry out calibration of QC laboratory equipment as required.
• Prepare and maintain stocks of reagents, solvents, chemicals and consumables as required.
• Work to maximise productivity and meet targets and deadlines with minimal personal errors.
• Maintain a high standard of laboratory work with regard to both practical output and documentation, including GMP standard work.
• Adhere to all documented procedures relating to the work carried out.