Remote Master Batch Record Designer (MES/Pharma)

GMP Pros®; Omaha (NE); Hybrid; USD 80,000 - 100,000; Full time

Job summary

GMP Pros® is seeking a Master Batch Record Designer in Omaha, Nebraska, to develop and maintain electronic Master Batch Records within a manufacturing execution system. The ideal candidate will have experience in the biotech or pharmaceutical industries and must understand regulatory standards.

This role offers remote work with occasional on-site requirements. Candidates should possess strong communication skills and experience with eBR systems like PAS-X.

Qualifications

• 3-5 years of experience in pharmaceutical manufacturing, quality assurance, or technical writing.
• Minimum of 2-3 years hands-on design experience with eBR systems.
• Knowledge of GMP, FDA 21 CFR Part 11, and relevant regulatory standards.

Responsibilities

• Develop, configure, and maintain electronic Master Batch Records.
• Work with project team to understand business requirements.
• Support integration of hardware and infrastructure.

Skills

Experience in biotech, pharmaceutical, or animal health industries

Hands-on design experience with electronic batch record systems

Mapping business processes (Visio, Lucid Chart)

Excellent communication and organization skills

Analytical and problem-solving mindset

Education

Bachelor’s degree in Life Sciences or related field

MES platform-based training or certification

Tools

PAS-X

Pharmasuite

Siemens opCenter

Job description

GMP Pros® is seeking a Master Batch Record Designer in Omaha, Nebraska, to develop and maintain electronic Master Batch Records within a manufacturing execution system. The ideal candidate will have experience in the biotech or pharmaceutical industries and must understand regulatory standards.

This role offers remote work with occasional on-site requirements. Candidates should possess strong communication skills and experience with eBR systems like PAS-X.