Description

You will develop, maintain, and optimize Werum PAS-X systems for pharmaceutical manufacturing processes.

This role is on-site.

Responsibilities

• Design, configure, and implement Werum PAS-X systems to integrate with manufacturing workflows.
• Develop, modify, and enhance MBRs and GMBRs on PAS-X V3 (v3.1 or higher).
• Maintain, troubleshoot, and optimize system uptime and efficiency.
• Ensure automation processes comply with GMPs and FDA guidelines.
• Maintain documentation, including SOPs and change control records.

Required Skills

• 7-10 years of experience in MBR Development within the Pharmaceutical Industry.
• 7-10 years of experience with Werum PAS-X (formerly Korber PAS-X).
• Strong knowledge of PMBR (Parameter Master Batch Records) and PVL (Parameter Value List).
• Deep understanding of GMP and FDA regulations.
• Bachelor’s degree in engineering, Computer Science, or a related field.
• Ability to manage multiple tasks and adapt to changing priorities.

Key Skills

Education

Any Gradute