Why join us ?
30 branches in France and locations on 5 continents will enable you to develop your career close to home and on the other side of the world. Specialising in consulting and engineering services for major pharmaceutical and biotechnological players, we offer our employees a challenging work environment where the culture of expertise and service, innovation, the human dimension and investment in employee training will make you enjoy the Ingérop Life Sciences experience.
Mission
On the missions undertaken by ILS, you will work independently or in collaboration with other experts in 3 main areas :
Definition of the Industrial Strategy
You will be involved in the definition of our clients’ industrial strategies, assisting them in :
– The definition of industrial master plans,
– Development plan for information management and “industry 4.0
– Support in de-industrialisation processes,
– Audit of industrial tools,
– Intervention on specific technical issues,
– Industrial due diligence.
Design implementation :
You will support our clients in the shaping of their industrial project, providing them with your expertise and experience in :
– Definition of the Site Master Plan,
– Definition of the solutions/systems to be implemented in the context of Industry 4.0,
– The industrial feasibility of your solutions,
– Deployment strategy of the considered solutions,
– Conceptual studies specific to these systems and installations,
– The strategy for qualification and validation of the considered installations,
– Pre-project studies.
Industrial implementation:
You will assist our clients in the follow-up of the deployment of the recommended solutions:
– Definition of the execution mode of relevant packages,
– Purchasing strategy,
– Support for the selection of partners,
– Audit, technical reviews of detailed studies,
– Management, steering of the packages until production start-up,
– Implementation of maintenance plans.
You will also take part in the development of the business by participating in seminars specific to your expertise and you will assist the sales department in the drafting and presentation of tenders.
Profile required
You have at least 15 years of experience in the definition, specification and deployment of industrial IT and automation solutions and their implementation in the pharmaceutical/biotechnology industry.
You are familiar with the qualification/validation of computerised or automated systems in accordance with FDA (21 CFR part 11), European GMP annex 11 and GAMP 5 regulations.
You are dynamic, autonomous and able to make proposals. You are rigorous and able to summarise and communicate effectively in writing and orally. You enjoy working in a team and have a sense of service.
Your intellectual curiosity and adaptability enable you to take an interest in and contribute effectively to a variety of projects.
Occasional international mobility and a very good knowledge of english are necessary for this position.