Review and optimize DeltaV control strategies and batch recipes for GMP manufacturing.
Define and test DCS logic, process handshakes, and system prompts to ensure robust process automation and compliance.
Provide on-floor and off-floor technical support for manufacturing operations including fermentation, centrifugation, and ultrafiltration processes.
Lead or contribute to change controls, CAPAs, and technical assessments related to process improvements or equipment modifications.
Act as Equipment Owner for assigned systems (e.g., bioreactors, centrifuges, TFF skids), managing lifecycle, reliability, and performance monitoring.
Participate in risk assessments, root cause analyses, and deviation investigations.
Collaborate with Manufacturing, QA, and Validation to define and implement production strategies, cleaning procedures, and work scopes.
Identify process optimization opportunities and lead implementation of improvements with cross-functional alignment.
Generate and review technical documentation, SOPs, protocols, and reports in compliance with cGMP standards.
Contribute to the promotion of Antaes services on top of assistance provided to clients.
Job Requirements
Bachelor degree in Science, Chemical Engineering, Mechanical Engineering, Manufacturing Engineering, Biotechnology, or related Life Science.
5 8 years experience in Engineering, pharmaceutical industry.
Strong knowledge of batch processing, handshakes, and system prompts with DeltaV systems.
Strong hands-on experience with fermentation, centrifugation, and ultrafiltration processes.
Experience with quality and process improvement methodologies and tools (Lean, Six Sigma, value stream mapping, FMEAs, DMAIC) is desired.
Adherence to safety protocols and global regulatory compliance.
Candidate must be highly motivated, be able to work independently as well as in a team and have good organizational and oral and written communication skills.
