Job Description:

• Contribute to Life Science projects for Antaes Asia clients
• Review, and optimize DeltaV control strategies and batch recipes for GMP manufacturing.
• Define, 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