Sanofi, a global biopharmaceutical leader, is inviting applications for the role of Executive Production at its Goa manufacturing facility in Verna Industrial Estate. This opportunity is ideal for B.Pharm graduates with 1–3 years of experience in tablet manufacturing, especially in granulation, compression, and GMP-regulated environments.
This role plays a critical part in ensuring high-quality medicine production, operational excellence, and strict compliance with GMP, Quality, and HSE standards. If you are looking for pharma production jobs in Goa with a reputed multinational company, this is a strong career move.
🏭 Job Overview
- Job Title: Executive Production
- Location: Verna Industrial Estate
- Employment Type: Full-time
- Experience Required: 1–3 Years
- Education: B.Pharm
- Industry: Pharmaceutical Manufacturing (Tablets)
🧪 Key Responsibilities
Production & Shift Management
- Allocate manpower and resources as per daily production plans
- Ensure completion of scheduled activities within standard timelines
- Maintain smooth process flow from dispensing to compression/coating
- Execute effective shift handovers and critical communications
Quality & GMP Compliance
- Ensure adherence to SOPs, BMRs, and GMP standards
- Identify, report, and support resolution of deviations, OOS, and OOT
- Compile and submit batch manufacturing records to QA
- Maintain data integrity and audit readiness at all times
Production Planning & SAP
- Execute production plans in coordination with cross-functional teams
- Ensure timely batch posting and WIP control in SAP
- Plan and manage equipment changeovers efficiently
Process Excellence & Continuous Improvement
- Improve cycle time, yields, and equipment utilization
- Update OEE data and support Lean and Six Sigma initiatives
- Implement productivity and cost-optimization projects
Training & People Development
- Train operators and new joiners on SOPs, GMP, and HSE
- Support validation documentation and new product transfers
- Act as a role model for compliance, discipline, and safety culture
HSE & Safety Compliance
- Implement site HSE systems and zero-incident culture
- Conduct daily +QDCI meetings and safety training
- Participate in departmental safety committee initiatives
Validation & New Product Introduction
- Prepare and execute validation protocols and reports
- Support pilot, engineering, and commercial batch validation
- Revise MFR/BMR post-validation as required
🎓 Qualifications & Skills
Educational Qualification
- B.Pharm (Mandatory)
Experience
- 1–3 years in pharmaceutical tablet manufacturing
Technical Skills
- Granulation, dispensing, compression, coating
- GMP documentation, audits, validation exposure
Software & Tools
- SAP, MS Word, Excel, PowerPoint
Language
- English (written and verbal proficiency required)
💼 Salary & Benefits
- Estimated Salary: ₹3.5 – ₹5.5 LPA (as per industry standards)
- Work at a state-of-the-art manufacturing facility
- Exposure to global quality systems and audits
- Strong learning, training, and career growth environment
- Inclusive workplace with equal opportunity policies
📩 How to Apply
