Technical Head

Strategic & Leadership

• Define and implement the technical strategy for the Pharma & Healthcare vertical in line with business goals.
• Lead, mentor, and manage all technical teams — including R&D, manufacturing, QA/QC, regulatory affairs, process development, and third-party manufacturing/sourcing partners.
• Direct and coordinate cross-functional teams and HODs (Head of Departments) across head office and manufacturing/factory operations.
• Oversee resource allocation, budgeting, and scheduling of technical operations including technology-transfer, process improvements, and product lifecycle management.

Research, Development & Manufacturing Oversight

• Oversee R&D and process development activities for APIs, formulations or healthcare products, from lab to commercial scale.
• Manage technology transfer activities — including sourcing of contract manufacturers or 3rd-party manufacturers, and supervising production start-ups.
• Ensure manufacturing processes are robust, validated, reproducible, and in compliance with regulatory requirements and industry best practices.

Quality Assurance, Regulatory Compliance & Safety

• Oversee QA/QC functions, ensuring raw materials, intermediates, and finished products meet defined quality, safety and regulatory standards.
• Ensure compliance with relevant regulatory guidelines (local and/or international), and lead documentation, regulatory filings, audits and inspections as applicable.
• Implement and maintain quality management systems, standard operating procedures (SOPs), and continuous improvement processes for safety, efficacy, and compliance.

Stakeholder & External Partner Management

• Liaise with senior management (e.g. CEO), business stakeholders, supply-chain teams, procurement, and external manufacturing / contract manufacturing organisations (CMOs) or third-party vendors.
• Lead vendor/third-party selection, qualification, audits, and ensure third-party compliance with required technical and regulatory standards.
• Coordinate with cross-functional departments (procurement, supply chain, regulatory, quality, operations, etc.) for seamless end-to-end product lifecycle management.

Reporting & Documentation

• Prepare and present periodic reports (progress, compliance status, production metrics, regulatory status, quality/defect metrics, improvement actions) to senior leadership and stakeholders.
• Maintain full oversight and documentation for R&D activities, technology transfers, manufacturing processes, QA/QC records, regulatory filings, and change-control programmes.

Continuous Improvement & Innovation

• Stay updated with emerging technologies, regulatory updates, best practices in pharma/healthcare manufacturing, process automation, lab automation, supply-chain technology and quality management. i-pharmconsulting.com+1
• Implement process improvements, cost-reduction, efficiency enhancement, risk-mitigation, and scale-up strategies without compromising quality or compliance.

Job Type: Full-time

Pay: ₹25,000.00 - ₹65,000.00 per month

Benefits:

• Cell phone reimbursement
• Flexible schedule
• Food provided
• Internet reimbursement
• Provident Fund

Work Location: In person