This is an 11-month initial contract.
Purpose An amazing opportunity has arisen for a QC Analyst in Analytical Testing.
In our start-up site the role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and Analytical Methods.
Responsibilities Perform a variety of routine Analytical techniques and associated documentation; including but not limited to Capillary Electrophoresis, UPLC, HPLC, GC, Wet Chemistry methods in compliance with GMP requirements Support activities including general lab readiness, audit readiness, laboratory equipment qualification and analytical method technical transfer, verification and validation Drive the development of technical skills through coaching and motivate a high performing culture across the team Foster a continuous improvement environment and bring strong problem solving and troubleshooting capabilities Consistently deliver on specific area Key Performance Indicators Operate to the highest standards of Safety, Quality and Compliance Demonstrate a commitment to learning and personal development that supports Quality, EHS, L&D and continuous improvement Requirements Degree qualification (Science/Quality/Technical) 1-3 years experience in the biotechnology and/or pharmaceutical industry, particularly in relation to Capillary Electrophoresis, UPLC, HPLC or GC testing Preferably Lean Six Sigma experience Ability to think logically and be proactive under pressure Ability to work as part of a team and on own initiative in a constructive manner Flexible and self-motivated Skills: HPLC UPLC Lean Six Sigma Analytical Testing