Sr. Manager

Job Title Sr Manager - Process Engineer- Biologics External Manufacturing Business Unit External Manufacturing and Supply Biologics Manager Title Head - External Manufacturing and Supply Operations Biologics Location Sun House Mumbai At Sun Pharma we commit to helping you Create your own sunshine - by fostering an environment where you grow at every step take charge of your journey and thrive in a supportive community Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world you ll find yourself becoming Better every day through continuous progress Exhibit self-drive as you Take charge and lead with confidence Additionally demonstrate a collaborative spirit knowing that we Thrive together and support each other s journeys Key responsibilities The Sr Manager Process Engineer will support the manufacture of Drug Product fill finish device assembly and secondary packaging of a biologics product The activities range from tech transfer technical process studies process validation activities data analysis to handling change controls deviations and troubleshooting Writing and reviewing of DP Device Assembly FG validation-related documents and key CMC sections of regulatory dossiers different countries are also required for this position Major Duties Responsibilities Lead and oversee the operational activities at DP FG Device Assembly CMOs scheduling of batches commercial manufacturing and testing of DP Responsible for achieving on-time in-full manufacturing of DP FG Device Assembly in compliance with approved dossiers in collaboration with Quality Assurance Regulatory Affairs and Analytical teams Serve as DP Subject Matter Expert SME on multidisciplinary CMC teams to ensure scientifically driven development and optimisation of biological processes Review and approve master batch records change controls and deviations CAPA to ensure GMP compliance and operational success Preparation and review of documents such as CPV reports risk assessments technical reports validation documents deviation reports and regulatory modules Responsible for Continuous Process Improvement and Process Optimization to reduce Cost of Goods Responsible for Tech Transfer and Process Validation into commercialisation Plan and forecast budgets analysing variances for production and development testing and execute the day-to-day financial activities in accordance with procedures and contracts The candidate will communicate across the organization to ensure key stakeholders are aware of project status potential risks and their required action plans Supporting post-launch market surveillance of the product Professional Experience Doctorate with 1-3 years of related experience - or- Master s degree and 3-5 years of related experience - or- Bachelor s degree and 5-7 years of direct experience in Biologics Drug Product GMP manufacturing Experience in cGMP Biologics Drug Product is a must Knowledge of statistical tools like Minitab JMP for data analysis is required Knowledge of analytical testing methods and their impact on product quality specifications is advantageous Skills Abilities Excellent interpersonal and communication presentation skills Excellent organizational and project management skills work well under pressure Ability to diagnose complex issues develop and implement solutions by collaborating with other teams Ability to influence internal and external stakeholders through scientific justifications Ability to thrive in a small group setting with limited administrative support Travel Estimate Job Requirements Educational Qualification B E BTech MS or Ph D degree in bio chemical engineering biotechnology Experience 5 years of experience in Manufacturing Factory CMO management Your Success Matters to Us At Sun Pharma your success and well-being are our top priorities We provide robust benefits and opportunities to foster personal and professional growth Join us at Sun Pharma where every day is an opportunity to grow collaborate and make a lasting impact Let s create a brighter future together Disclaimer The preceding job description has been designed to indicate the general nature and level of work performed by employee within this classification It is not designed to contain or be interpreted as a comprehensive inventory of all duties responsibilities and qualifications required of employees as assigned to this job Nothing herein shall preclude the employer from changing these duties from time to time and assigning comparable duties or other duties commensurate with the experience and background of incumbent s