Mumbai, Maharashtra, India
Not disclosed
On-site
Full Time
🚨 We're Hiring: #Production #Manager – Pharma OSD & External Preparations 🚨 Location: Plot No.1019, Vill. - Sarigam, G.I.D.C. , Road No. 10, Dist. - Valsad, Gujarat, India 396155. Industry: Pharmaceuticals #OSD & External Preparations) Experience: Minimum 10-12 Years We are looking for a highly experienced Production Manager to lead our Pharma OSD and External Preparation Plant. The ideal candidate will have in-depth knowledge of production processes, R&D-F&D coordination, excipient functionality, and a strong track record in team management to achieve production targets. Key Responsibilities: Lead daily operations of #OSD and external preparation manufacturing lines Collaborate closely with R&D/F&D for tech transfer and scale-up Ensure optimum utilization of resources to meet production goals Oversee compliance with GMP and regulatory standards Drive continuous improvement and process efficiency Requirements: B.Pharm/M.Pharm with 10-12 years of solid experience in pharmaceutical production Expertise in OSD (Tablets/Capsules) and External Preparations (Creams/Ointments) Strong knowledge of excipients, formulation, and plant operations Proven leadership in managing cross-functional production teams If you're ready to take the next step in your pharma career and thrive in a dynamic environment, we’d love to hear from you! 📩 Apply Now or DM us to know more. 📧 Send your resume to: hrd@tajpharma.com Call us: Mob: 9099511459 #Hiring #PharmaJobs #ProductionManager #PharmaceuticalIndustry Show more Show less
Umargam, Gujarat, India
None Not disclosed
On-site
Full Time
Responsible for managing and overseeing all production activities of the Oral Solid Dosage (OSD) plant, including planning, execution, supervision, and continuous improvement of manufacturing operations to ensure timely, cost-effective, and GMP-compliant production of tablets, capsules, and powders. --- Key Responsibilities: Lead day-to-day operations of the OSD manufacturing area. Ensure adherence to cGMP, regulatory, and safety guidelines. Plan production schedules and manpower allocation as per market demands. Coordinate with QA, QC, Maintenance, and Supply Chain for smooth operations. Review batch manufacturing records (BMRs) and documentation. Monitor production yields, deviations, and implement corrective/preventive actions. Train and supervise production staff and operators. --- Qualifications: B.Pharm / M.Pharm with 12–15 years of experience in OSD production. Strong knowledge of regulatory requirements (USFDA, EU, WHO-GMP). Proven leadership and problem-solving skills.
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