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Hiring : MBR Engineer with 5-7 years of experience in the pharmaceutical industry with a focus on MBR Development on Werum PAS-X systems, GMP, FDA regulations, Proficiency in Werum PAS-X Exp. at Raritan, New Jersey, USA
Email: [email protected]
From:

Narayana Rao 3MKLLC,

3MK Software Solutions LLC

[email protected]

Reply to:   [email protected]

Hello,

Greetings for the day!!!

Please review the below roles and advise the best time to connect with you. If you are interested, you can reach me on Linkedin: 

www.linkedin.com/in/narayanarao2

and
share resumes to

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Hiring : MBR Engineer with
5-7 years of experience in the
pharmaceutical industry with a focus on
MBR Development on Werum PAS-X systems,
GMP, FDA regulations,
Proficiency in
Werum PAS-X Exp.

Location: Raritan, NJ (Hybrid)

Duration: 6 Months

Rate : Open / hr

Job Description:

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.

Qualifications:

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

Bachelors degree in engineering, Computer Science, or a related field. Master's 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
MBRs and GMBRs on PAS-X V3 (V 3.1.8 or higher)

Validation and
UAT of MBRs\\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 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 PAS-X systems.

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

Thanks & Regards,

Narayana Rao

Sr Manager (Recruitments)

3MK Software Solutions LLC

Direct: 801-416-0999, India Contact Number : +91 8309310531

Email: 

[email protected]

Website: 

http://3mkllc.com/

Connect me
on Linkedin too for daily updates and REQUIREMENTS:

linkedin.com/in/narayanarao2

Note: 
WANT TO GET MY DIRECT CLIENT REQUIREMENTS DAILY

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Keywords: New Jersey
Hiring : MBR Engineer with 5-7 years of experience in the pharmaceutical industry with a focus on MBR Development on Werum PAS-X systems, GMP, FDA regulations, Proficiency in Werum PAS-X Exp.
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Fri Jun 14 03:06:00 UTC 2024

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Location: Raritan, New Jersey