Automation Engineer

X4 Life Sciences; Paris; Hybride; EUR 55 104 - 96 432; Temps partiel

Résumé du poste

A global consultancy in Life Sciences is seeking an experienced MES Specialist to support digital transformation in the pharmaceutical sector across France and BENELUX. The role involves leading MES system design and validation using Rockwell Pharma Suite. Candidates should possess 5-8 years of related experience and a relevant degree. This position offers a competitive hourly rate and flexibility with remote work.

Qualifications

• 5-8 years of industry experience.
• Experience in MES integration with other Level 2 & Level 3 systems.
• Extensive knowledge of MES, particularly Rockwell Pharma Suite.

Responsabilités

• Lead or support MES system design, configuration, testing, and validation activities.
• Prepare and review System Development Life Cycle (SDLC) deliverables.
• Contribute to MES design workshops alongside vendors, site integrators, and site representatives.
• Ensure compliance with global policies and cGMP standards.

Connaissances

MES integration

Technical proficiency with Rockwell Pharma Suite

Microsoft tools (Excel, SharePoint, Word, PowerPoint)

Formation

Bachelor's or master's in Engineering, Computer Science, or related field

Description du poste

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 12-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: 5-8 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 [e-mail]

Seniority level

• Mid-Senior level

Employment type

• Contract

Job function

• Engineering, Manufacturing, and Information Technology

Industries

• Pharmaceutical Manufacturing and Biotechnology Research

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