Engineering Project Manager for Pharma & Medical devices

PQE is a service provider company, leader in Pharmaceutical and Medical Device sectors since 1998. With a network of over 250 dedicated consultants, PQE delivers the highest level of expertise to more than 160 customers worldwide.

An international group, PQE operates in over forty countries throughout Europe, Asia and the Americas. PQE offers a worldwide coverage with offices and representatives across Europe, Asia, the Middle East and Latin America, in order to better serve these specific local markets. Further information can be found at www.pqe.eu.

Due to a constant growth, PQE is looking for a Project Manager expert in facilities, process equipment, utilities and related control systems qualification in the regulated pharmaceutical and medical devices environments.

Responsibilities include, but are not limited to, the following:

• Development of qualification plans, user/technical requirements specifications, design qualification reports, test plans, requirements-testing traceability matrixes, qualification summary reports

• Development of installation, operational and performance qualification protocols for equipment and utilities (e.g.: HVAC, Water Systems, Process Gases), according to the current internationally recognized guidelines (e.g.: ISPE, GAMP)

• Development of thermal validation study protocols

• Development of project validation master plans for new sites implementation including detailed Gantt charts with predecessors and resources workload evaluation (advanced knowledge of Microsoft Project requested)

• Knowledge of the main test instruments suites (e.g.: GE Kaye Validator, Thermal validation studies data loggers, HVAC test instruments, calibration instruments)

• Coordination of junior resources for qualification testing execution and use of test instruments

• Development of risk based assessment at process, component and functional level according to the internationally recognized methodologies (e.g.: FMEA, HACCP)

• Development of calibration and maintenance plans and related instructions

• Development of standard operating procedures

• Advanced knowledge of EU and US GMP

Requirements:

• Fluent English

• Technical Degree (Engineering, Chemistry, Informatics, Physics, Mathematics)

• Minimum of 3 years' experience in the drug manufacturing area

• Full availability to travel

• Integrity, strong analytical skills and attention to detail

Nice to have:

• Fluent in other languages

• PhD in technical fields

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