In the exciting and dynamic fields of the Pharmaceutical and Medical Device industries? We are currently seeking an experienced.
Lead and
execute commissioning, qualification, and validation activities pharmaceutical / biotech equipment systems
Prepare, review, and execute C&Q and validation documentation URS, DQ, IQ, OQ, PQ protocols test scripts summary reports ).
with cross-functional teams Engineering, QA, Validation, Manufacturing to ensure compliance with regulatory guidelines
Provide project updates progress reports stakeholders or related field.
Ability to work independently in a Fluent in Spanish written and spoken ).
PQE Group gives you the opportunity to work on international projects, improve your skills and interact with colleagues from all corners of the world.
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