Overview
Job title:
Exciting opportunity for an experienced MES specialist to support a world-class consultancy on a long-term project, driving digital transformation within the Life Sciences sector.
We are looking for MES engineers for a 1
- month contract to deliver cutting-edge Manufacturing Execution System (MES) solutions for leading pharmaceutical organisations across France and the BENELUX region.
The Company:
Our client is a global consultancy at the forefront of Life Sciences, helping major pharmaceutical and biotech organisations revolutionise their technologies and accelerate innovation.
You’ll be part of a high-performing team using advanced MES platforms like Rockwell Pharma Suite to lead or support MES system design, configuration, testing, and validation activities.
Role:
MES Specialist (Pharmaceutical)
Responsibilities
- Lead or support MES system design, configuration, testing, and validation activities
- Prepare and review System Development Life Cycle (SDLC) deliverables in line with internal quality standards
- Contribute to MES design workshops alongside vendors, site integrators, and site representatives
- Ensure all activities are carried out in compliance with global policies, procedures, regulatory requirements, and cGMP standards
Qualifications
- Education:
Bachelor’s or master’s in Engineering, Computer Science, or related field.
- Experience:
- 8 years of industry experience
- Experience in MES integration with other Level 2 & Level 3 systems
- Extensive knowledge & technical proficiency of MES, particularly Rockwell Pharma Suite.
- Proficiency with Microsoft tools (Excel, SharePoint, Word, PowerPoint)
The Logistics
- Initial 12 month project, 40 hours per week
- Mainly remote with some travel required as needed
- Competitive hourly rate, dependent on experience level
Apply below or email your CV direct to ******
Seniority level
Employment type
Job function
- Engineering, Manufacturing, and Information Technology
Industries
- Pharmaceutical Manufacturing and Biotechnology Research
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