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Expert Biotech Process - limited contract
A career at our company is an ongoing journey of discovery: our 58,000 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Biotech process expert - limited contract (CD Max) of 11 months
Purpose of the role:
Support Manufacturing areas in organizing and documenting automation activities, but also deviation investigations, process equipment changes and associated validation activities.
Key Tasks & Responsibilities
Write and support functional specification in specific project and/or for small modicifactions
Coordinate all testing activities regarding testing implementation
Participate to project as automation SME
Be the single point of contact for automation in the production department
Project/ Production activities
Understand in a complete manner the activities and processes of production.
Ensure that all operations are performed according to cGMP rules
Implement or support new equipment installation or improvement modification projects
related to process equipment and methods.
Ensure a proper definition (URS), design, execution, validation and documentation of
these new equipment or improvement projects in compliance with cGMPS an in respect of
project timelines and costs.
Manage and participate to testing activities and to their documentation in line and cGMP
Write or review project validation plans and reports as appropriate and coordinate their
Production Support to Investigations:
Ensure expertise support to Operations
Participate to the improvement of the production operations management
Ensure homogeneous practices between different operational areas.
Support production in developing technical solutions for operational problems and/or
Support production on investigations from deviations
Report to management, to area supervisors and/or to project teams on the progress of the
EDUCATION/ PROFESSIONAL EXPERIENCE
Mechanical or Chemical Engineering Degree (bachelor minimum, masters preferred)
Experience in equipment qualification and/or process validation in international
pharmaceutical or biotech companies and sound awareness of cGMP related issues
Project Management Experience in a cross functional environment
Excellent problem solving skills, both conceptual and practical.
Good understanding of operations tasks and engineering/design.
Hands-on experience in start-up and troubleshooting of process equipment in large scale
Familiar with automation / programmation language
Knowledge of Yokogawa / DeltaV is an asset
Very good knowledge of French, spoken and read, advantage if written
Very good knowledge of English, read/written/spoken
What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at https://jobs.vibrantm.com