Job Description

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.
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Skills Required