About Akkodis
Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation. With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC. Akkodis offers broad industry experience, and strong know-how in key technology sectors such as mobility, software & technology services, robotics, testing, simulations, data security, AI & data analytics. The combined IT and engineering expertise brings a unique end-to-end solution offering, with four service lines – Consulting, Solutions, Talents and Academy – to support clients in rethinking their product development and business processes, improve productivity, minimize time to market and shape a smarter and more sustainable tomorrow.
Akkodis is part of the Adecco Group. Our Webstite : www.akkodis.com
Context :
Ensure the qualification (from the design phase to the end of validation) of equipment, facilities, computerized systems, and utilities, while adhering to Good Manufacturing Practices (GMP) and hygiene and safety regulations, in accordance with the site’s Validation Master Plans (VMP).
Responsibilities:
* Ensure the ongoing auditability of validation and qualification documentation for installations.
* Define and monitor qualification/validation strategies.
* Write qualification/validation documents in compliance with GMP.
* Coordinate, execute, and/or verify qualification tests for installations and utilities (e.g., HVAC, thermal validation, etc.), involving future users and in accordance with current procedures. This includes managing potential deviations and monitoring associated quality systems.
* Propose innovative solutions that are compatible with the various chemical and pharmaceutical requirements in force and the company’s objectives.
* Manage relationships with suppliers, the final design of equipment, tracking of P&IDs, electrical schematics, and project execution (planning, coordination, etc.).
Profile :
* Over 5 years of experience in pharmaceutical companies, with project management experience, preferably in CAPEX projects within commercial GMP facilities.
* Knowledge of qualification/validation techniques for equipment used in production.
* Strong technical expertise in upstream and downstream processes.
* Good knowledge of automated systems, with knowledge of Siemens PCS7 being an asset.
* Good understanding of cGxP requirements.
* Ability to take responsibility and make decisions.
* Experience in laboratory equipment validation is a plus.
* Languages: English mandatory; French is a plus but not required.
Why can't you refuse this offer?
As a member of the AKKODIS team, you will be:
* Integrated into your role through a buddy system process
* Supported in your career by your Business Manager
* An active participant in your training plan and personal and professional development
* Benefiting from a permanent contract
* Receiving a competitive salary package that includes several extra-legal benefits