Are you a precise and technically strong professional with experience in validating automated systems within a pharmaceutical environment?
Then this position as Support CSV Automation Engineer could be the perfect next step in your career.
We are looking for someone who takes ownership of computer system validation, collaborates closely with project stakeholders, and maintains a strong focus on quality. You will join an environment where technology, compliance, and teamwork go hand in hand.
What will you do?
As a Support CSV Automation Engineer, you are responsible for the validation of systems and software within a regulated (GxP) pharmaceutical environment. You will work closely with engineering, production, quality and maintenance teams, ensuring that all systems meet legal and client requirements.
Your responsibilities include:
* Defining functional, technical, and quality requirements
* Supporting the design and engineering of automation solutions (PLC, DCS, SCADA, HMI, MES…)
* Detecting and eliminating errors in products and software development
* Communicating with project stakeholders (management, production, quality, maintenance…)
* Preparing, reviewing and executing validation documentation (IQ, OQ, PQ)
* Performing commissioning and decommissioning tests
* Supporting FAT and SAT activities with suppliers and monitoring vendor quality
* Drafting URS, DQ, SRA, TCD and ERES documentation
* Identifying quality issues and preparing reports
* Advising on quality improvements and best practice implementation
* Ensuring compliance with GMP, Eudralex, FDA and EHS guidelines
* Managing changes in accordance with change control principles
* Testing and validating automation systems and processes
Hard Skills
Minimum requirements:
* Master’s degree in Industrial Engineering, Production Management, Engineering or equivalent
* OR
* Bachelor’s degree with at least 8 years of relevant experience in validation within the pharmaceutical industry.
Experience & expertise:
* At least 5 years of experience in CSV, automation, or validation within a regulated/Gxp environment
* Strong knowledge of at least two of the following systems: Siemens PCS7 / TIA Portal - Emerson DeltaV - Archestra - Rockwell
* Strong communicator & team player
* Excellent French; English plus
* Good documentation & basic Excel
What do we offer?
With us, you choose stability, variety and a career in which quality and expertise are central. You will have access to challenging technological projects in a regulated environment.
You can count on:
* Permanent contract or freelance collaboration
* Competitive salary package with various extra-legal benefits
* Company car with fuel card
* 13th month, annual bonus and monthly net allowance
* 32 days of leave
* Meal and eco vouchers
* Hospitalisation and group insurance
* Training opportunities through our internal Academy
* A warm community and enjoyable team events
Who are we?
We are an international project sourcing partner with many years of experience in technical and industrial sectors. Our consultants do not choose just one project, but a career full of variety, growth, and craftsmanship.