Overview:
Expleo offers a unique offering of integrated engineering, quality and strategic consulting services for digital transformation. In a context of unprecedented technological acceleration, we are the trusted partner of innovating companies. We help them develop a competitive advantage and improve the daily lives of millions of people. Present in 30 countries and with 18,000 employees, we support our customers on a daily basis. As part of our teams, you will carry out various advisory and support missions with our clients.
Joining Expleo means:
* Technical support in the field Continuing training via our technical experts
* Human values among our employees
* The diversity of our teams An increase in skills throughout your career
* Work on large-scale projects
Responsibilities:
* Review the URS provided by the project Leader or the Customer in order to ensure all requirements mentioned related with its area of expertise are understandable and realistic
* Add all technical request in the URS for the commissioning and qualification request.
* Realize and provide the technical solution for design related issue with its area of expertise to the technical coordinator and Project leader
* Responsible for the Safety by design (with support of the internal HSE representative)
* Ensure every days that the work planned has been completed regarding the schedule
* Communicate the day to day schedule to the technical coordinator
* Ensure a good communication with other SMEs linked to its activity (Battery limits)
* Check quality of execution on site and record observations/findings in the punchlist
* Act as package owner for commissionning and verification (writing protocols and test sheets, review reports and treat incident/deviations) until hand-over;
* The complete power distribution from HV to LV including transformer, UPS, emergency generator
Qualifications:
* Proven experience in CAPEX project
* 5+ years of experience in the engineering for industrial and/or pharmaceutical environment
* Experience of biotech environment in the bio-pharmaceutical industry is preferred.
* Knowledge of safety, GMP and environmental regulatory requirements.
* Experience in legal conformity and energization process (3 green lights)
* Proven experience in qualification ; knowledge of Verification (ASTM E2500) is a plus
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