fortil
About the Company
Fortil is an engineering group and technology consulting, a model designed by entrepreneurial engineers. Working with Fortil means working with an ambitious and expert community, driven by accuracy, challenge and emulation.
Today, more than 2,000 of us work every day to make Fortil the largest independent engineering company in Europe.
Our ambition is to contribute to building a more responsible, communal and inclusive world for our employees and clients.
Find out more on fortil.group
Listed Jobs
- Company Name
- fortil
- Job Title
- Développeur C/C++ systèmes embarqués F/H
- Job Description
-
Vos responsabilités métier :
Participer à la conception et au développement de solutions logicielles intégrant à la fois des systèmes embarqués et leurs serveurs backend.
Travailler sur des projets liés aux caméras connectées et au traitement de flux vidéo.
Contribuer à l’implémentation de modules pour des environnements distribués.
Assurer la communication entre différents systèmes en se basent sur différents protocoles.
Participer à la rédaction de la documentation technique et au transfert de compétences aux équipes.
Profil recherché
Vos atouts pour réussir :
Vous avez une expérience en IoT et une maîtrise des protocoles de communication IoT, notamment MQTT et ZMQ.
Vous avez une maîtrise des solutions complexes mêlant vidéos, traitements de données et gestion de systèmes à faible consommation d'énergie
Votre profil & personnalité :
Issu(e) d’une formation Bac+5 cycle Ingénieur
Vous justifiez d’une expérience de minimum 4 ans sur du développement C/C++ dans un environnement embarqué
Vous êtes capable de sortir de votre zone de confort et d’être force de proposition dans un écosystème potentiellement complexe
Vous êtes organisé.e et bon communiquant.e afin de transmettre la bonne information au bon interlocuteur
Cagnes-Sur-Mer, France
On site
09-01-2025
- Company Name
- fortil
- Job Title
- Lead Process (H/F)
- Job Description
-
Vos responsabilités métier
Produce and Review the URS in order to ensure all User requirements are fully respected
Include all technical requests in the URS for the commissioning and qualification.
Prepare Tender package and participate in discussions for supplier decision.
Define the applicable standards/norms/engineering guidelines for the project
Provide suppliers with the applicable standards
Challenge technical solutions coming from suppliers
Integrate safety, sustainability and green assessment in the design
Define List of Deliverables for his/her discipline
Provide project deliverables of his/her discipline to Process Lead
Track supplier’s planning adherence for installation of systems. Progress report to be delivered to Process and technical lead
Organize quality checks on field before each technical milestone activity
Communicate the day to day schedule to the Process and Technical Leads
Ensure a good communication with other stakeholders linked to its activity (Battery limits)
Maintain his knowledge accuracy based on new technology. Keep up-to-date
Write the specifications related with its area of expertise and provide the document to the Process Lead for review
Define battery limit and RACI matrix with Process Lead
Update drawings in its area of expertise
Write commissioning documentation and ensure that the supplier's documentation is acceptable to perform verification (ASTM 2500)
Perform FAT/SAT activities in its area of expertise
Support the qualification phases after commissioning (V-Cycle and/or ASTM2500)
Organize the training of the final user in its area of expertise & provide technical documentation in to finalize the hand-over
Actively perfom the tasks to an efficient Hand-over in its area of expertise, with the follow-up of the associated punchlist
Respect documentation strategy
Qualifications
10+ years of relevant experience in large scale EPCMV Projects in the pharmaceutical industry
In-depth technical experience in a regulated environment with knowledge of gene therapy, biologicals, pharmaceutical and engineering operations
Good Expertise in automated systems within the large scale pharmaceutical industry
Leading the Process & Automation team
Large experience in basic/detailed design, equipment installation and commissioning
Driving consistency within Engineering standards, norms and regulations
Supporting qualification and validation activities
Ensuring adherence to EHS regulation and Green good practices.
Large Experience with EPCMV (Engineering, Procurement and Construction Management & Validation) contracting models is mandatory.
Ability to lead package in collaboration with suppliers from design to qualified status.
Ability to lead & review PED (Pressure Equipment Directive) is a relevant asset
Ability to act as technical process expert during HAZOP (Hazard and Operability study) / QRA (Quality Risk Analysis) / FMEA
Knowledge in qualification & validation approaches (ASTM E2500) is highly important
Good technical knowledge in bioprocess equipment (USP, DSP, media/buffer) and their applicability.
Good knowledge in automated systems (Siemens PCS7) and understanding of IT security requirements (data integrity)
Strong knowledge of cGMP/GLP regulations, ICH, FDA CMC, ISPE and PDA Guidance Documents is preferred.
Experience in large and complex projects as well as both formal and informal leadership / coordination
Capable to benchmark with peers in the industry and able to identify latest trends
Excellent communication skills in order to present frequent reports to Management.
Antwerp, Belgium
On site
29-01-2025