Head MS&T DS CoE

Sandoz India

Telangana

On-site

INR 6,000,000 - 10,000,000

Full time

3 days ago
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Job summary

Sandoz India seeks a senior Process Science leader to establish a world-class CoE for biologics manufacturing across platforms. You will develop roadmaps for fed-batch, intensified and continuous processes, harmonize standards, and act as a global SME for process performance and robustness.

The role drives governance for investigations, data-driven manufacturing, and advanced process control, while leading cross-functional teams and ensuring state-of-the-art CPV and regulatory readiness.

Qualifications

  • MSc or PhD in a relevant scientific field.
  • 15+ years in Biologics Manufacturing, MS&T, Process Development or Technical Operations.
  • 7+ years leading technical organizations.
  • Experience supporting commercial biologics manufacturing.
  • Deep expertise in upstream and/or downstream processing.
  • Proven technology transfer leadership experience.
  • Experience supporting regulatory inspections.

Responsibilities

  • Provide end-to-end technical oversight of biologics manufacturing processes.
  • Lead global SME efforts for process performance, characterization and robustness.
  • Drive process improvement via governance, investigations and CAPA.
  • Support CPV, validation lifecycle, and regulatory submissions.
  • Oversee technology transfer into and out of manufacturing sites.
  • Lead and develop Process Science leaders and build multi-site capabilities.
  • Foster innovation with digital and analytics-driven manufacturing.
  • Partner with Regulatory Affairs, Quality and Supply Chain to ensure compliance.

Skills

Process science leadership
Biologics manufacturing
Continuous manufacturing
Digital analytics / data-driven
Process characterization
Technical governance
Strategic leadership
Cross-functional collaboration

Education

MSc in Biotechnology, Biochemical Engineering, Pharmaceutical Sciences, Chemical Engineering, Biology, or related
PhD in relevant scientific discipline (preferred)

Job description

Major Accountabilities
Organizational Leadership
  • Establish a world-class Process Science CoE supporting all biologics manufacturing platforms.
  • Develop technical roadmaps for improvement in fed-batch, intensified and continuous manufacturing technologies.
  • Drive harmonization of scientific standards, best practices and technical governance across all manufacturing sites.
  • Establish the CoE as the central knowledge hub for drug substance manufacturing processes.
Scientific & Technical Leadership
  • Provide end-to-end technical oversight of upstream and downstream manufacturing processes.
  • Serve as global SME for commercial biologics process performance, process characterization and process robustness.
  • Lead scientific assessment of process performance trends, process capability and manufacturing excellence initiatives.
  • Provide governance for complex technical investigations, atypical events and major product-impact assessments.
  • Drive deployment of advanced process control strategies and data-driven manufacturing approaches.
Manufacturing Support
  • Ensure timely scientific support for routine commercial manufacturing.
  • Act as escalation point for critical manufacturing issues, deviations, and product impact assessments.
  • Lead complex technical investigations and root cause analyses.
Process Lifecycle Management
  • Own lifecycle management of commercial manufacturing processes.
  • Drive process robustness, yield improvement, productivity enhancement, and cost optimization initiatives.
  • Ensure effective Continued Process Verification (CPV) and process monitoring programs.
Technology Transfer
  • Support/Lead transfers of commercial and development products into and out of the site.
  • Ensure effective transfer of process knowledge, control strategies, and manufacturing expertise.
  • Establish risk-based transfer plans and governance structures.
Validation and Compliance
  • Provide technical leadership for process characterization, PPQ, comparability and validation lifecycle activities.
  • Support global regulatory submissions and agency interactions.
  • Maintain inspection readiness across the manufacturing network.
  • Provide scientific justification and technical defense during regulatory inspections.
Innovation & Emerging Technologies
  • Evaluate emerging manufacturing technologies and industry trends.
  • Drive adoption of advanced analytics, digital twins, AI-enabled manufacturing and predictive process monitoring.
  • Build partnerships with equipment suppliers, technology providers and academic institutions.
  • Sponsor innovation programs improving manufacturing flexibility, robustness and cost competitiveness.
People Leadership
  • Lead and develop global Process Science leaders and subject matter experts.
  • Build organizational capability in USP, DSP and continuous manufacturing.
  • Establish succession planning and talent pipelines.
  • Foster a culture of scientific excellence, collaboration, innovation and accountability.
Stakeholder Management
  • Serve as technical representative to Global MS&T, Regulatory Affairs, Quality, Supply Chain, and Manufacturing Operations.
  • Lead technical governance forums and cross-functional decision-making processes.
Competencies
Leadership Competencies
  • Strategic Leadership
  • Scientific Excellence
  • Business Acumen
  • Stakeholder Management
  • Organizational Development
  • Change Leadership
  • Talent Development
  • Decision Making
  • Innovation Mindset
  • Continuous Improvement
Key Performance Indicators
Supply & Manufacturing Excellence
  • Supply reliability (% batches released / no supply interruptions)
  • Right-First-Time (RFT) manufacturing rate
  • Process yield achievement
  • Process capability (CpK/PpK) for critical processes
Quality & Compliance
  • Critical/major inspection observations
  • Overdue deviations and CAPAs
  • Recurring deviation rate
  • Products maintained in validated state
Lifecycle & Technical Delivery
  • Technology transfers delivered On-Time-In-Full (OTIF)
  • Process validation / CPV milestones achieved
  • Lifecycle change implementation success rate
  • Technical project milestone adherence
Continuous Improvement
  • Yield, throughput, or productivity improvements delivered
  • Cost savings/value generation from process improvements
  • Digital/PAT implementation milestones achieved
People & Organization
  • Employee engagement score
  • Talent retention and succession readiness
  • Training compliance
Ideal Background
Education Minimum
  • MSc in Biotechnology, Biochemical Engineering, Pharmaceutical Sciences, Chemical Engineering, Biology, or related scientific discipline
Preferred
  • PhD in relevant scientific discipline
Languages
  • Fluent English (written and spoken)
Experience Minimum
  • 15+ years in Biologics Manufacturing, MS&T, Process Development, or Technical Operations
  • 7+ years leading technical organizations
  • Experience supporting commercial biologics manufacturing
  • Deep expertise in upstream and/or downstream processing
  • Proven technology transfer leadership experience
  • Experience supporting regulatory inspections
Preferred
  • Continuous manufacturing experience
  • Perfusion manufacturing experience
  • Advanced process control and PAT experience
  • Global network leadership experience
  • Multi-site manufacturing support experience
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