Officer – Production & GMP Compliance
Location: Pithampur, Madhya Pradesh, India
Company: Lupin
Date Posted: February 7, 2026
Employment Type: Full-Time
Industry: Pharmaceutical Manufacturing | Production Operations | Quality & Compliance
About the Role
Lupin is seeking a dedicated Officer – Production & GMP Compliance at its Pithampur facility. This role is responsible for ensuring smooth production operations, compliance with GMP/GxP standards, and effective coordination across QC, R&D, Engineering, and QA teams.
The ideal candidate will have a strong understanding of pharmaceutical manufacturing processes, quality systems, validation, and regulatory compliance. This is a critical role for optimizing production efficiency while maintaining high standards of safety and product quality.
Experience Required
Relevant experience in pharmaceutical manufacturing, production, or operations
Exposure to GMP/GxP compliance, process troubleshooting, and quality management systems
Experience in coordinating cross-functional teams and managing production workflows
Educational Qualification (Mandatory)
Bachelor’s or Master’s degree in Pharmacy, Life Sciences, Biotechnology, or related field
Key Responsibilities
Production & Process Management
Plan and execute departmental activities in line with delivery schedules
Ensure proper handling and availability of raw materials, bulk, and finished goods
Optimize utilization of manpower, machinery, and materials
Monitor production workflows and allocate tasks effectively
Compliance & Quality Assurance
Adhere to all GMP, GxP, EH&S, and other regulatory requirements
Complete SOP training and perform tasks according to applicable procedures
Report deviations, non-conformities, or operational issues to QA and management
Maintain hygiene, discipline, and cGMP compliance across production areas
Validation & Continuous Improvement
Oversee validation and qualification activities; prepare and review relevant documents
Implement corrective and preventive actions (CAPA) for deviations, complaints, or non-conformities
Support change control implementation and process improvement initiatives
Troubleshoot machinery and production processes to ensure operational efficiency
Cross-Functional Coordination
Collaborate with QC, R&D, Engineering, QA, and other departments
Ensure smooth communication and timely resolution of operational challenges
Contribute to continuous improvement initiatives to enhance productivity and compliance
Additional Responsibilities
Support quality management systems
Undertake any other assignments allocated by the Unit Head
Required Skills & Competencies
Strong knowledge of pharmaceutical production processes and cGMP compliance
Analytical and problem-solving skills for process and equipment troubleshooting
Excellent organizational and multitasking abilities
Effective collaboration and stakeholder management skills
Attention to detail and result-oriented approach
Core Competencies
Strategic Agility
Process Excellence
Collaboration & Teamwork
Innovation & Creativity
Result Orientation
Stakeholder Management
Customer Centricity
Developing Talent
Why Join Lupin?
Work in a regulated, high-standard pharmaceutical manufacturing environment
Gain exposure to cross-functional teams and advanced production systems
Contribute to compliance-driven operations in a globally recognized company
Enhance expertise in process optimization, validation, and GMP-compliant manufacturing
Equal Opportunity Statement
Lupin is committed to providing equal employment opportunities across recruitment, promotion, compensation, and professional development. All qualified candidates will be considered in accordance with applicable regulatory requirements.
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