MES Engineer

  • Raritan, NJ
  • Posted 1 day ago | Updated 1 day ago

Overview

On Site
Depends on Experience
Accepts corp to corp applications
Contract - Independent
Contract - W2
100% Travel

Skills

MES
Management
Manufacturing
Operational Efficiency
Optimization
Pharmaceutical Industry
Communication
Conflict Resolution
Process Optimization
Project Management
Change Control

Job Details

Role Name: MES Engineer

Location: New York, NY / Raritan, NJ

Job Description
Position Overview: As a Senior MES PAS-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum PAS-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes.
Key Responsibilities:
Development\Modification\Upgrade\Enhancement of MBR s and GMBR s on PAS-X V3 (V 3.1.8 or higher)

Validation and UAT of MBR s\GMR\ESP

Werum PAS-X Implementation: Design, configuration, and implementation of Werum PAS-X systems to ensure seamless integration with existing pharmaceutical manufacturing processes.

Project Leadership: Take charge of MBR Development, from inception to completion, ensuring adherence to project timelines and budget constraints.

Compliance: Ensure all automation processes comply with industry regulations, including GMP (Good Manufacturing Practices) and FDA guidelines.

System Maintenance: Oversee the maintenance, troubleshooting, and optimization of Werum PAS-X systems to ensure maximum uptime and operational efficiency.

Validation: Manage the validation and qualification processes for developed MBR s, ensuring they meet user requirement and specification.

Documentation: Maintain comprehensive documentation of automation processes, including SOPs (Standard Operating Procedures) and change control documentation.

Training: Provide training and support to colleagues and team members to ensure their proficiency in Werum PAS-X systems.

Continuous Improvement: Identify opportunities for process optimization and efficiency improvements within the automation systems and propose solutions.

Qualifications:

Minimum of 5-7 years of experience in the pharmaceutical industry with a focus on MBR Development on Werum PAS-X systems.

Bachelor s degree in engineering, Computer Science, or a related field. Masters degree is a plus.

Strong knowledge of GMP, FDA regulations, and industry best practices.

Proficiency in Werum PAS-X and other pharmaceutical automation systems.

Project management experience, with the ability to lead cross-functional teams.

Excellent problem-solving skills and the ability to work effectively in a team-oriented environment.

Strong communication and documentation skills.

Ability to adapt to changing priorities and manage multiple tasks simultaneously.

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