| MES(Manufacturing Execution System) Analyst Opportunity in Raritan, NJ - Onsite. at Raritan, New Jersey, USA |
| Email: [email protected] |
| Hello, Role: MBR Analyst Work location: RARITAN (US:08869), NJ Duration: 10+months JOB DESCRIPTION: Position Overview: As a Senior MES Client-X MBR Modeler you will play a critical role in the design, implementation, and maintenance of our MBR using Werum Client-X V2/V3. You will ensure compliance with industry standards and regulations while optimizing production processes. Key Responsibilities: Development\\Modification\\Upgrade\\Enhancement of MBRs and GMBRs on Client-V2\\V3 Validation and UAT of MBRs\\GMR\\ESP Werum Client-X Implementation: Design, configuration, and implementation of Werum Client-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 Client-X systems to ensure maximum uptime and operational efficiency. Validation: Manage the validation and qualification processes for developed MBRs, 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 Client-X systems. Continuous Improvement: Identify opportunities for process optimization and efficiency improvements within the automation systems and propose solutions. Qualifications: Minimum of 5-8 years of experience in the pharmaceutical industry with a focus on MBR Development on Werum Client-X systems. Bachelors 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 Client-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. Please let me know if you would like to discuss this compelling opportunity further. If the opportunity above isnt the right fit for you at the moment, but know someone in your network that may be looking for this type of role, I would love to connect with them. Thanks, Mansi Kukreja Technical Recruiter Direct#: (925) 393- 5851 [email protected] www.axiomglobal.com Integrity. Expertise. Results. -- Keywords: information technology New Jersey |
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| Fri Feb 09 00:58:00 UTC 2024 |