Company Name: Celogen Pharma Pvt. Ltd.
Position Title: Production Executive
Department: Production
Location: Ponda, Goa
About Celogen:
Celogen Pharma Pvt. Ltd. is a growing pharmaceutical manufacturing company engaged in the development and manufacturing of high-quality pharmaceutical formulations for domestic and international markets. The company operates three advanced manufacturing facilities, including a dedicated hormone manufacturing unit at Mehsana and two other manufacturing units at Daman and Goa. With a strong focus on quality, compliance, hygiene, and operational excellence, Celogen Pharma is committed to delivering safe, effective, and affordable healthcare solutions while maintaining high standards across all its operations.
Position Summary
The Production Executive is responsible for executing and monitoring manufacturing activities in accordance with current Good Manufacturing Practices (cGMP), approved Standard Operating Procedures (SOPs), and regulatory requirements. The role involves ensuring smooth production operations, maintaining accurate documentation, optimizing resource utilization, and supporting quality and compliance objectives.
Key Responsibilities
Production Operations
- Execute daily manufacturing activities as per approved production plans and schedules.
- Ensure production processes are carried out in accordance with BMRs, BPRs, SOPs, and cGMP requirements.
- Monitor production activities to achieve planned output and maintain product quality standards.
- Coordinate with Warehouse, Quality Assurance, Quality Control, Engineering, and PPIC teams for uninterrupted production operations.
- Ensure timely completion of manufacturing activities and associated documentation.
Documentation & Compliance
- Maintain and review Batch Manufacturing Records (BMRs), Batch Packing Records (BPRs), equipment logbooks, and other production-related documents.
- Ensure all documentation is completed accurately and in compliance with GMP requirements.
- Report deviations, incidents, and non-conformances to the reporting manager and participate in investigations and CAPA implementation.
- Adhere to company policies, SOPs, and regulatory requirements at all times.
Manpower & Process Management
- Supervise production operators and technicians during manufacturing activities.
- Ensure proper utilization of manpower, equipment, and materials.
- Conduct on-the-job training and guide team members on GMP and operational requirements.
- Monitor cleanliness, line clearance, and readiness of production areas before commencement of activities.
Equipment Management
- Ensure proper operation and utilization of manufacturing equipment.
- Coordinate with the Engineering department for preventive maintenance and breakdown resolution.
- Verify equipment cleaning status, calibration status, and operational readiness before use.
Quality & Regulatory Compliance
- Ensure compliance with cGMP, Good Documentation Practices (GDP), and data integrity requirements.
- Support internal audits, customer audits, and regulatory inspections.
- Implement corrective and preventive actions arising from audits, deviations, and investigations.
- Maintain production areas in an audit-ready condition.
Safety, Health & Environment
- Follow all safety procedures
- Ensure the use of prescribed Personal Protective Equipment (PPE) within production areas.
- Report unsafe conditions, incidents, and near misses promptly.
Continuous Improvement
- Identify opportunities for productivity improvement, waste reduction, and process optimization.
- Support initiatives aimed at improving operational efficiency and product quality.
Experience & Educational Qualifications
- Bachelor’s Degree in Pharmacy is required. Master’s Degree in Pharmaceutics is preferable.
- 2 - 3 years of relevant experience in pharmaceutical manufacturing operations is required.
- Experience in handling production activities in a GMP-regulated pharmaceutical environment will be preferred.
Required Skills & Competencies
- Sound knowledge of pharmaceutical manufacturing processes and cGMP requirements.
- Understanding of Batch Manufacturing Records (BMR), Batch Packing Records (BPR), SOPs, and Good Documentation Practices (GDP).
- Ability to supervise shop-floor activities and manage production personnel effectively.
- Strong problem-solving, analytical, and decision-making skills.
- Good communication, coordination, and interpersonal skills.
- Ability to work in a cross-functional team environment.
- Attention to detail and commitment to quality and compliance.
- Knowledge of safety practices and regulatory requirements applicable to pharmaceutical manufacturing.
- Proficiency in basic computer applications such as MS Office and production documentation systems.
Pay: ₹30,000.00 - ₹55,000.00 per month
Ability to commute/relocate:
- Ponda, Goa (Ponda): Reliably commute or planning to relocate before starting work (Required)
Work Location: In person
