QC Analyst

at  BioTechne

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

WE ARE LOOKING FORWARD TO READING YOUR APPLICATION.

In order to qualify for this position, you will need to be authorised to live and work in the UK.
At Bio-Techne we appreciate and value diversity. We are seeking to attract, develop and retain talented people that will contribute to the overall success of our business. We have a supportive and flexible working environment, with commitment from all levels of the organisation in promoting equality.

• 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.