Your new company

Leading company in the Pharmaceutical Industry

Your new role

• Perform document analytical testing
• Review document equipment verification and calibration
• Investigate abnormalities
• Support lab investigations and perform equipment troubleshooting
• Author GMP documentation
• Be part of continuous improvement projects

What you'll need to succeed

• Degree in Chemistry or equivalent
• 1 year of QC experience in analytical laboratory

What you'll get in return

You will be part of a leading company who values employees and have a structured career growth and development opportunities.

You will also be compensated with attractive remuneration

What you need to do now

If you're keen on pursuing this exciting opportunity, please send a copy of your CV (word document) to geraldine.tay@hays.com.sg or contact Geraldine at +6560272244

Hays Registration Number: 200609504D, EA License No: 07C3924, Registration ID No.: (R22105664)

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