21545-QC Analyst-Meath Contractor

This is an 11-month initial contract.

Purpose 

In our start-up site the role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and/or 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.
• Review and approve Analytical Testing data.
• 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).
• 3-5 years’ experience in the biotechnology and/or pharmaceutical industry, particularly in relation to Capillary Electrophoresis, UPLC, HPLC, CE and or raw materials testing.
• 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.
• Problem solving abilities.