Automation Engineer

JOB DESCRIPTION Designation Deputy Manager Level 7 - II Job Location Bangalore The Company Syngene International Ltd BSE 539268 NSE SYNGENE ISIN INE398R01022 is an integrated research development and manufacturing solutions company serving the global pharmaceutical biotechnology nutrition animal health consumer goods and specialty chemical sectors Syngene s 4500 scientists offer both the skills and capacity to deliver great science robust data management and IP security and quality manufacturing at speed to improve time-to-market and lower the cost of innovation With a combination of 1 9 Mn sq ft of specialist discovery development and manufacturing facilities as well as dedicated research facilities for Amgen Baxter Bristol-Myers Squibb and Herbalife Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA Position Summary We are seeking a highly skilled and motivated Process Automation Engineer with a strong background in biopharmaceutical process design and or manufacturing The ideal candidate will bring hands-on expertise in automation systems particularly within Upstream operations and add on experience in Downstream operations chromatography ultrafiltration diafiltration nanofiltration This role offers the opportunity to work on cutting-edge projects in process automation recipe management and control system design using advanced platforms and will extend to digital transformation Functional Responsibilities Design develop and implement automation solutions for Upstream and downstream operations Develop process control strategies in compliance with ISA S88 standards for batch process automation Create configure and validate recipe management systems for complex biopharma operations Design and implement PLC-based control systems using platforms such as Siemens WinCC PCS7 or similar Configure and maintain DCS platforms including Siemens PCS7 and or DeltaV from Emerson Collaborate with cross-functional teams including process engineering validation manufacturing and quality Troubleshoot and resolve automation-related issues during project execution or manufacturing daily operations Author and review automation documentation including design specifications FRS SDS HDS URS FAT SAT and validation protocols Implementing minor and major expansion projects on site and changes targeting optimisation as part of the operational support Primary Responsibilities Project Ownership Accountable for the successful execution of projects from initiation through completion ensuring all deliverables meet client expectations and regulatory standards Quality Assurance Responsible for ensuring that all processes comply with cGMP and other regulatory requirements thereby safeguarding product quality and patient safety Client Satisfaction Ensure high levels of client satisfaction through effective communication timely updates and proactive problem-solving Compliance and Risk Management Identify and mitigate risks associated with technology transfer ensuring that all operations are compliant with internal and external guidelines Develop and validate process maps and models in collaboration with cross-functional teams Adapt to additional tasks and responsibilities as assigned demonstrating flexibility and a proactive approach Education B Tech M Tech in Industrial Process Engineering Automation Engineering Instrumentation Electrical Engineering Chemical Engineering or related fields 7-10 years of relevant industry experience in biopharmaceutical automation process design commissioning or manufacturing support In-depth knowledge of biotech manufacturing processes with specialization in Upstream automation not limited to process including software writing and IT infrastructure Experience with PLC and SCADA DCS platforms Siemens WinCC PCS7 DeltaV or comparable systems Proficient in batch process control recipe creation as per ISA S88 is a must Strong understanding of instrumentation P IDs control strategies and process control hardware software integration Knowledge of GAMP5 21 CFR Part 11 compliance and other regulatory guidelines Hands-on experience in project executions including qualification phase IQ OQ PQ and on-floor operations Excellent communication and documentation skills Preferred Attributes Experience with single-use technologies SUT and Stainless-Steel technologies in bioprocessing Prior involvement in facility design or greenfield brownfield projects Experience working with digital plant systems or in digital transformation initiatives in biopharma Exposure to data historians automation analytics and real-time monitoring systems Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity EEO to all persons regardless of age color national origin citizenship status physical or mental disability race religion creed gender sex sexual orientation gender identity and or expression genetic information marital status status with regard to public assistance veteran status or any other characteristic protected by applicable legislation or local law In addition Syngene will provide reasonable accommodations for qualified individuals with disabilities Pls visit us at to know more about us and what we do