Process Engineer H/F

  • Assystem Energy & Infrastructure
  • France
  • déc. 16, 2020
Contrat CDI

Description

At our customer, you will be the first point of contact for manufacturing with regard to process-specific problems related to production installations (e.g. filling lines, packaging machines, autoclaves, reactors, formulation tanks, ...). Your responsabilities will be the following: You coordinate long-term projects on the one hand and you ensure direct follow-up of the daily routine process on the other; You monitor the production process, analyze problems and make proposals for improvement in terms of process efficiency, quality and reliability; You determine the process control strategy and when problems arise, you conduct a root cause investigation and risk assessment; In case of adjustments and improvements to the production process, you ensure that process validation is carried out and that the necessary technical documents (e.g. work instructions, procedures, ...) are available; You are responsible for setting up improvement tests and you also like to roll up your sleeves to sometimes carry out these tests yourself; You can be involved in the implementation, validation and start-up of new production installations. You ensure a close follow-up of the entire process and you facilitate a streamlined collaboration between the various internal departments (such as QA, production, purchasing, ...) and external partners You hold a Master's Degree as an engineer (bio, civil, industrial etc.), industrial pharmacist etc... You have a first solid technical experience in a production environment A knowledge of GMP standards is a plus You have a strong project management and planning skills You have a service-oriented attitude    You have a good knowledge of French and/or Dutch and English, both written and spoken 

Description entité

Depuis 50 ans, nous sommes animés par la conviction que les ingénieurs, par leur audace, leur expertise et leur capacité à faire bouger les lignes sont les architectes du monde de demain. Tous les jours, nos 5 700 collaborateurs innovent au contact de leurs clients. Ils accompagnent les plus grands projets de l'ingénierie mondiale dans les domaines de l'énergie, de la santé, des sciences de la vie et des transports. Groupe international en forte croissance, nous sommes présents dans 14 pays (Europe, Moyen-Orient, Asie, Afrique). Acteur reconnu pour notre expertise en CQV (Commissioning Qualification Validation) et experts des projets à fortes contraintes techniques et réglementaires, nous accompagnons les laboratoires pharmaceutiques et industries de pointe dans leurs investissements et leurs enjeux liés à la sécurité et à la diminution des coûts et des délais de mise sur le marché. Pour nos clients, nous innovons et intégrons des technologies disruptives dans les domaines de l'intégrité des données, la cybersécurité et la maintenance prédictive.

Entité

Assystem Care

Mission

At our customer, you will be the first point of contact for manufacturing with regard to process-specific problems related to production installations (e.g. filling lines, packaging machines, autoclaves, reactors, formulation tanks, ...). Your responsabilities will be the following: You coordinate long-term projects on the one hand and you ensure direct follow-up of the daily routine process on the other; You monitor the production process, analyze problems and make proposals for improvement in terms of process efficiency, quality and reliability; You determine the process control strategy and when problems arise, you conduct a root cause investigation and risk assessment; In case of adjustments and improvements to the production process, you ensure that process validation is carried out and that the necessary technical documents (e.g. work instructions, procedures, ...) are available; You are responsible for setting up improvement tests and you also like to roll up your sleeves to sometimes carry out these tests yourself; You can be involved in the implementation, validation and start-up of new production installations. You ensure a close follow-up of the entire process and you facilitate a streamlined collaboration between the various internal departments (such as QA, production, purchasing, ...) and external partners

Profil

You hold a Master's Degree as an engineer (bio, civil, industrial etc.), industrial pharmacist etc... You have a first solid technical experience in a production environment A knowledge of GMP standards is a plus You have a strong project management and planning skills You have a service-oriented attitude    You have a good knowledge of French and/or Dutch and English, both written and spoken 

Métier

Support et Contrôle de Production

Date de publication

déc. 16, 2020

Secteur

Sciences de la Vie