RESPONSIBILITIES
- Specify, design, develop, document, test and implement Manufacturing Execution Systems for a growing client base
- Author, develop and configure Electronic Batch Records (EBR)
- Implement MES solutions and integrate with ERP and control equipment
- Document MES configuration and validation of EBRs;
- Collaboratively partner with client accounts and internal teams to deliver on multiple large-scale projects
REQUIREMENTS
- Bachelors’ degree in Science, Engineering or relatable technical degree
- 3 – 7 years of experience in a highly automated Life Sciences manufacturing environment
- Experience with at least on one of these PAS|X, Syncade, PharmaSuite, XFP, POMS, Camstar or other life sciences compatible MES solutions
- Knowledge of FDA and GMP guidelines
- Working knowledge of software Development Life Cycle (SDLC) and support methodologies
- Understanding of Life Sciences validation processes required