Sterile Manufacturing Equipment Validation Engineer

MaViAl Sp. z o.o. is recruiting an experienced Sterile Manufacturing Equipment Validation Engineer for full-time, on-site work in Monza, Lombardy, Italy.

Main responsibilities:

• Plan and execute qualification and validation activities for sterile manufacturing equipment, clean utilities and controlled environments.
• Prepare and run installation, operational and performance qualification protocols with complete traceable evidence.
• Review user requirements, design documents, commissioning records, calibration status and vendor documentation.
• Investigate protocol deviations, document root causes and coordinate corrective or preventive actions with Quality and Engineering.
• Maintain validation reports, traceability matrices and lifecycle records in accordance with approved GMP procedures.

Requirements:

• At least five years of pharmaceutical equipment qualification, validation or commissioning experience.
• Degree or technical qualification in engineering, pharmaceutical technology, chemistry or biotechnology.
• Practical knowledge of IQ, OQ and PQ, risk-based validation, change control, deviations and data integrity.
• Ability to interpret P&IDs, equipment specifications, clean-utility documentation and validation acceptance criteria.
• Driving licence valid in Italy and sufficient English for controlled documentation and safety communication.

The base rate is €29.00 gross per hour for 40 hours per week. Work is based at an assigned sterile pharmaceutical manufacturing facility in Monza. Applications are accepted only through the official OpeningsHub resume form.

This Sterile Manufacturing Equipment Validation Engineer opening is tied to Monza, Lombardy, IT. Candidates should compare their experience with the responsibilities and qualifications below before applying; employment type: full time; published working pattern: 40 hours per week; on-site validation schedule confirmed in the written offer; published compensation: 29.0 EUR per hour.