Job Description
Job Description - 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.
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