O
Orchid Pharma
Cluster Head
Skills
Testing & QAComplianceRegulatory Compliance
18 days ago
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Important information
Contract type:
Permanent
Location:
Kotputli, Rajasthan 303108, India
Work mode:
Onsite
Published on:
9 October 2026
What they need
Key Responsibilities:
- Independently manage overall site operations covering Production, QA/QC, Engineering, EHS, Warehouse and Utilities.
- Ensure smooth manufacturing of API and finished formulations in compliance with cGMP, regulatory and statutory requirements.
- Drive production planning, operational efficiency, cost optimization and plant performance.
- Lead site-level audits, CAPA, compliance and continuous improvement initiatives.
- Ensure effective plant maintenance, utilities management and EHS standards.
- Provide strategic leadership and build a high-performance site team.
- Coordinate with corporate functions and ensure achievement of business and operational objectives.
Candidate Profile:
- 20+ years of overall experience in pharmaceutical manufacturing.
- Minimum 5 years of independently handling a manufacturing site/plant.
- Strong experience in API and finished formulations.
- Chemical Engineering/Chemical Technology preferred.
- Strong knowledge of cGMP, regulatory compliance, EHS and plant operations.
- Proven leadership and stakeholder management capabilities.
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