Manufacturing Process Engineer
MPE_4304017448
Posted: 23/09/2025
- New Jersey, United States (On-site)
- Contract
About the Role
Are you passionate about precision, compliance, and innovation in pharmaceutical manufacturing? We’re seeking a Recipe Author with expertise in Emerson Syncade MES to design and optimize electronic batch records (EBRs) that directly support the safe and efficient delivery of life-changing medicines.
Key Responsibilities
- Design, configure, and maintain GMP-compliant recipes within Syncade MES.
- Translate manufacturing and process requirements into structured, efficient, and compliant electronic workflows.
- Partner with process engineers, QA, validation, and IT teams to ensure recipes align with both operational and regulatory requirements.
- Troubleshoot, refine, and optimize existing recipes to improve efficiency, reduce errors, and support continuous improvement initiatives.
- Maintain all recipe documentation in line with FDA, EMA, and other international regulatory standards.
About You
- Hands-on experience authoring recipes in Emerson Syncade MES within a pharmaceutical or biotech setting.
- Strong knowledge of GMP and regulatory compliance, with a proven track record in EBR design.
- Analytical and problem-solving skills with the ability to convert complex manufacturing processes into intuitive workflows.
- Excellent communication and teamwork skills, able to collaborate across multiple functions.
- Degree in Engineering, Computer Science, Life Sciences, or related field (or equivalent practical experience).
Sam Walker
Client Services Director
