An amazing opportunity has arisen for a QC Analyst in Analytical Testing at a single-use Multiproduct Biotech facility. In this role, you will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and Analytical Methods. This is an 11-month contract, onsite position with a pay rate of up to 30 euro per hour depending on experience.
What you will do:
1. Bring energy, knowledge, innovation, and influence to carry out the following:
2. Perform a variety of routine Analytical techniques and associated documentation, including but not limited to Capillary Electrophoresis, UPLC, HPLC, GC, and Wet Chemistry methods in compliance with GMP requirements.
3. Support activities including general lab readiness, audit readiness, laboratory equipment qualification, and analytical method technical transfer, verification, and validation.
4. Drive the development of technical skills through coaching and motivate a high-performing culture across the team.
5. Foster a continuous improvement environment and bring strong problem-solving and troubleshooting capabilities.
6. Consistently deliver on specific area Key Performance Indicators.
7. Operate to the highest standards of Safety, Quality, and Compliance.
8. Demonstrate a commitment to learning and personal development that supports Quality, EHS, L&D, and continuous improvement.
What skills you will need:
1. Degree qualification (Science/Quality/Technical).
2. 1-3 years’ experience in the biotechnology and/or pharmaceutical industry, particularly in relation to Capillary Electrophoresis, UPLC, HPLC, or GC testing.
3. Preferably Lean Six Sigma experience.
4. Ability to think logically and be proactive under pressure.
5. Ability to work as part of a team and on your own initiative in a constructive manner.
6. Flexible and self-motivated.
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