Bio-Techne is a world-leading developer and manufacturer of high-quality biological reagents and is seeking a QC Analyst to join their growing team in their QC department 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.

Requirements:

• Degree level in chemistry or related science
• Minimum 1 years+ QC experience (experience in a GMP environment would be advantageous), experience 3 years+ is desirable.
• Detailed knowledge of analytical chemistry
• High level of personal and independent productivity
• Possess excellent verbal and written communication skills
• Decision making and problem-solving skills
• Practical ability and analytical data interpretation skills
• Collaborative and team work skills
• IT skills and competency with Microsoft software packages
• Safe and responsible working manner in laboratory areas

Roles & Responsibilities:

• Work in a safe and responsible manner, abiding by the COSHH regulations and maintaining a high level of tidiness.
• To be familiar with all required QC and analytical techniques through on the job training and external courses where appropriate.
• 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.
• 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.