The role involves performing routine manufacturing processes and equipment preparation such as CIP, PT, and SIP while ensuring strict adherence to GMP guidelines
Job Summary
The role involves performing routine manufacturing processes and equipment preparation such as CIP, PT, and SIP while ensuring strict adherence to GMP guidelines.
Candidates must be capable of troubleshooting process-related issues and communicating effectively with supervisors regarding safety or quality irregularities.
This is a 1-year contract position with an option for extension based on performance, requiring the ability to carry loads up to 10kgs.
Matching Summary
Match Score: 75
The role involves performing routine manufacturing processes and equipment preparation such as CIP, PT, and SIP while ensuring strict adherence to GMP guidelines.
Skills & Requirements
Must-have
GMP compliance experience
Electronic Batch Record (EBR) usage
Rotating 12-hour shift work availability
Equipment preparation skills
Process troubleshooting capabilities
Nice-to-have
Team player with analytical skills
Knowledge of downstream processing
Experience with LIMS, SAP, DCS, MES software
Key Requirements
Degree/Diploma/ITE in chemical engineering, pharmaceutical, or biotechnology