Company Overview
SM Biologics offers innovative biopharma design services, guiding clients through discovery and development with cutting-edge solutions to achieve efficient and effective outcomes.
Job Summary
Apply your expertise in biopharmaceutical processes and equipment to support commissioning, qualification, and validation activities within a cGMP cleanroom environment, ensuring compliance and operational excellence.
Responsibilities
- Apply knowledge of DeltaV control systems to support process automation and control in biopharmaceutical operations
- Execute commissioning, qualification, and validation activities following cGMP standards to ensure regulatory compliance and product quality
- Implement FAT, SAT, IQ, OQ, and PQ protocols to verify equipment and system performance in biopharmaceutical manufacturing
- Interpret engineering drawings and P&IDs to guide installation, troubleshooting, and maintenance of biopharmaceutical equipment
- Operate effectively within a biopharmaceutical cleanroom environment, adhering to contamination control and safety procedures
- Support biopharmaceutical process workflows by applying technical knowledge of equipment and process requirements
