Designation Upstream Manufacturing Documentation Job Location Bangalore About Syngene Syngene is an innovation-led contract research development and manufacturing organization offering integrated scientific services from early discovery to commercial supply At Syngene safety is at the heart of everything we do personally and professionally Syngene has placed safety at par with business performance with shared responsibility and accountability including following safety guidelines procedures and SOPs in letter and spirit Key Result Areas Role-specific Lead the upstream process group to design and develop cell culture processes for monoclonal antibody and fusion protein production Provide expert leadership overseeing both strategic and day-to-day activities in upstream process development of complex novel biologics Oversee technology transfer to support scale-up and GMP manufacturing Build strong relationships with CMOs to optimize efficiency productivity quality and supply assurance Design and execute risk-based process characterization studies to define critical process parameters CPPs and critical quality attributes CQAs Scale-up process from laboratory-scale bioreactors to pilot and commercial-scale ensuring process robustness and consistency in compliance with regulatory requirement Prepare technology transfer protocols descriptions and execute transfer to clinical and commercial manufacturing sites Collaborate with downstream processing analytical development and quality assurance teams to ensure seamless integration of upstream processes Liaise with regulatory affairs to ensure compliance with industry standards and guidelines Analyze experimental data to draw meaningful conclusions and make data-driven decisions Prepare and present technical reports project updates and scientific findings to senior management and stakeholders Ensure that all upstream processes are compliant with cGMP ICH FDA EMEA regulatory requirements Prepare and review process descriptions and CMC sections of regulatory documents to support regulatory submissions as required for IND and BLA Develop and implement strategic plans to achieve project milestones and goals Mentor and develop team members to foster a high-performance culture Education Master s degree bachelor s degree in pharmacy master s degree in Pharmaceutical Sciences Industry Experience Minimum 5 -10 years of relevant practical experience in mAbs Upstream process and documentation Other competencies required for the role Excellent problem-solving skills and ability to work in a fast-paced collaborative setting Experience with automation and data analysis tools applied for cell culture bioprocessing Familiarity with regulatory submissions and quality systems in the biopharmaceutical industry Strong interpersonal skills with ability to work with internal and external stakeholders Excellent written and verbal communication skills for regulatory documentation and presentations Strong knowledge of bioprocessing principles cell culture techniques and scale-up methodologies Perform review of protocols study protocols equipment qualification protocols etc Review the executed protocols and provide adequate support for timely closure of the same Preparation of general upstream related procedures protocols risk assessment and BMRs On-time initiation closure of deviations investigations CAPA and change controls Safety and DI Responsibilities Adhere to organizational policies procedures on EHSS POSH Data Integrity and IT security Always wear the applicable PPEs and adhere to any other Environment Health and Safety EHS requirements in the workplace for individuals lab plant safety Understand all necessary safety protocols and always follow the same to ensure safety for all Proactively identify near-misses potential incidents and communicate to supervisor and or line manager or through the respective web portals 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

📌 Upstream Manufacturing Documentation (Bengaluru)
🏢 Syngene International
📍 Bengaluru