Overview
Skills
Job Details
Role: MES Engineer
Location: New York, NY / Raritan, NJ
Interview: Phone/Skype
Job Type: Contract
JOB DESCRIPTION:
PAS-X Senior Engineer
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.
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.?