Minimum of 6+ years of experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech industry.
Proven Upstream system and CIP / SIP knowledge.
Minimum 6+ years of experience in commissioning / qualification / validation of Downstream systems.
Experience with DeltaV (Emerson).
Fluent English language written and verbal communication skills.
cGMP knowledge and knowledge of regulatory requirements.
Able to work with minimum oversight fulfilling deliverables within target dates.
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