Work Schedule
Standard (Mon-Fri)Environmental Conditions
OfficeJob Description
Are you looking to make a significant impact in the pharmaceutical manufacturing industry Join Thermo Fisher Scientific Monza as a Production Support Expert and be part of an exceptionally driven team dedicated to advancing world-class pharmaceutical production!
Maintain pharmaceutical sterile injectables production compliance with US and EU GMP and company quality standards through prevention and intervention suggestions.
Control
Mantain continuous surveillance of the production lines for sterile forms (cleaning blending functionality defects) to ensure adherence to current regulations and company quality benchmarks.
Engage in outlining and orchestrating testing and validation procedures for machinery ensuring alignment with current regulations and company quality criteria.
Participate in self-audits and implement corrective actions to maintain regulatory compliance.
Analyze and determine necessary actions to remove the causes of defects and complaints.
Propose and participate in GMP training courses applicable to production activities based on control findings.
Contribute to the issuance and revision of procedures and work sheets ensuring their application during operational phases.
(A) ESSENTIAL:
Italian
English
Previous involvement in manufacturing sterile and oral injectable medications
Join us and help ensure flawless production processes while working collaboratively in an ambitious environment. Your expertise will be key to our success!
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