M
Mankind Pharma
MDI & DPI Manager
Skills
Performance ManagementBudgetingInternal AuditComplianceRegulatory Compliance
2 months ago
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Important information
Contract type:
Permanent
Location:
Paonta Sahib, Himachal Pradesh, India
Work mode:
Onsite
Published on:
10 August 2026
What they need
Role & responsibilities
- Lead the establishment, commissioning, qualification, and commercialization of MDI (Metered Dose Inhaler) and DPI (Dry Powder Inhaler) production and packing lines.
- Manage end-to-end manufacturing operations including production planning, execution, packing, and dispatch activities.
- Ensure compliance with cGMP, USFDA, MHRA, EU-GMP, WHO-GMP, and other regulatory requirements.
- Develop, implement, and maintain Quality Management Systems (QMS) including Deviations, CAPA, Change Control, Risk Assessment, SOPs, Investigations, and Audit Compliance.
- Drive technology transfer, process validation, equipment qualification (DQ/IQ/OQ/PQ), and cleaning validation activities.
- Establish robust manufacturing and packing processes to achieve productivity, quality, and cost targets.
- Lead and manage cross-functional teams comprising Production, Packing, Engineering, Warehouse, and Quality departments.
- Ensure effective manpower planning, team development, performance management, and succession planning.
- Monitor and improve key performance indicators (KPIs) such as OEE, productivity, yield, rejection, and compliance metrics.
- Lead regulatory, customer, and internal audits and ensure timely closure of observations.
- Implement Lean Manufacturing, Operational Excellence, and Continuous Improvement initiatives.
- Ensure adherence to EHS (Environment, Health & Safety) standards and promote a strong quality culture.
- Manage budget planning, resource utilization, and cost optimization projects.
- Provide strategic leadership for capacity expansion, new product introductions, and operational excellence programs.
Preferred candidate profile
- B.Pharm/M.Pharm/B.Tech/M.Sc. with 8-15 years of experience in MDI & DPI production and packing operations in a regulated pharma environment.
- Proven expertise in establishing and commissioning MDI & DPI manufacturing and packing lines, including qualification and validation activities.
- Strong knowledge of QMS, cGMP, regulatory compliance, technology transfer, audit management, CAPA, and change control systems.
- Demonstrated leadership skills with experience in team management, operational excellence, productivity improvement, and cross-functional coordination.
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