
Head Drug Substance Operations , MSAT , Planning & Transformation
- Hyderabad, Telangana
- Permanent
- Full-time
- Scale up capacity to address ~8X increase of demand through Opex and productivity interventions
- Ensure facility readiness to serve regulated markets
- Digitize the core and implement Digital 4.0 in operations
- Streamlining Production Planning & Scheduling to provide unconstrained service to front end markets (OTIF-100%)
- Capacity augmentation by new facility set up and acquisition
- Strengthen the MSAT & ASAT organizations to scale to 10X manufacturing outpu
- Conduct a comprehensive evaluation of the organization's preparedness for scaling operations.
- Design a strategic roadmap for expansion, focusing on capacity, capability, technology, and infrastructure development.
- Lead cross-functional teams in executing transformation initiatives effectively.
- Strengthen manufacturing and R&D capabilities to support biosimilar scale-up, ensuring timely product delivery and audit compliance.
- Drive the adoption of innovative technologies and process enhancements to optimize performance at scale.
- Track project milestones, analyze key performance indicators (KPIs), and ensure progress aligns with objectives.
- Implement change management strategies to enable seamless transitions to new processes and systems.
- Leverage data analytics and insights to improve decision-making, streamline operations, and enhance overall efficiency.
- Identify, evaluate, and mitigate risks to ensure business continuity while maintaining regulatory compliance.
- Oversee all aspects of biosimilars drug substance manufacturing, ensuring compliance with GMP and regulatory standards.
- Lead and manage the manufacturing services and technology teams to optimize production processes and improve efficiency.
- Develop and implement manufacturing strategies to meet production goals and timelines.
- Drive transformation initiatives to enable scale-up to 8X, achieving best-in-class productivity.
- Ensure all manufacturing plants are audit-ready and capable of supplying products without constraints.
- Ensure the highest standards of quality control and assurance throughout the manufacturing process.
- Collaborate with cross-functional teams, including R&D, Quality, and Regulatory Affairs, to support product development and commercialization.
- Drive continuous improvement initiatives to enhance manufacturing capabilities and reduce costs.
- Manage the technology transfer process for new products and processes.
- Ensure compliance with all safety, health, and environmental regulations.
- Develop and manage the manufacturing budget, including capital expenditures and operational costs.
- Mentor and develop team members, fostering a culture of innovation and excellence.
- Develop the scale up transformation roadmap with respect to capacity, capability, technology and infrastructure. Introduce new technologies and process improvements that will significantly scale the performance
- Bachelor's degree in Biochemistry, Biotechnology, Chemical Engineering, or a related field. Advanced degree preferred.
- Minimum of 15 years of experience in biologics manufacturing, with at least 5 years in a leadership role
- Extensive knowledge of biosimilars manufacturing processes, including upstream and downstream processing.
- Strong understanding of GMP, regulatory requirements, and quality control standards
- Proven experience in managing large-scale manufacturing operations and leading cross-functional teams
- Track record of clearing FDA audits and scaling manufacturing operations
- Past experience in introducing new technologies and interventions for improving performance
- Experience of leading teams ~400+
- Experience with single-use bioreactor technology and continuous manufacturing processes.
- Knowledge of process development and technology transfer.
- Familiarity with regulatory submissions and inspections.