Executive - Tablet Manufacturing

SAVA HEALTHCARE LIMITED; Indor; On-site; INR 500,000 - 700,000; Full time

Job summary

SAVA HEALTHCARE LIMITED is looking for an Executive – Tablet Manufacturing at our Indore (Regulated Pharma Manufacturing Plant) facility. You will support day-to-day tablet production, including granulation, compression, and coating, following BMR/SOPs and ensuring cGMP compliance.

Key duties include line clearance with QA, in-process checks (hardness, weight, disintegration, friability) and strict data integrity.

Qualifications

• Experience in regulated pharmaceutical manufacturing (USFDA / MHRA / WHO-GMP).
• B.Pharm / M.Pharm / B.Sc. (Science) degree is required.
• 2–5 years of relevant experience in regulated pharma manufacturing.

Responsibilities

• Execute operations related to granulation, compression, and coating as per BMR and SOPs.
• Operate, clean, and maintain equipment such as RMG, FBD, tablet press, auto coaters.
• Perform line clearance in coordination with QA.
• Ensure in-process checks like weight variation, hardness, thickness, disintegration, friability.
• Maintain documentation with GDP and Data Integrity.
• Report deviations, breakdowns, and process abnormalities to supervisors.
• Monitor adherence to safety protocols and housekeeping in manufacturing area.
• Participate in validation and qualification activities.

Skills

cGMP

SOPs

Tablet manufacturing

Education

B.Pharm / M.Pharm / B.Sc. (Science)

Tools

RMG

FBD

Tablet press

Auto coaters

Job description

Job Description – Executive: Tablet Manufacturing

Job Title: Executive – Tablet Manufacturing

Location: Indore – Regulated Pharma Manufacturing Plant

Department: Production – Oral Solid Dosage (OSD)

Reporting To: Manager / Sr. Manager – Manufacturing

Job Type: Full-Time | Executive Level

Job Purpose

To execute and monitor day-to-day operations in tablet manufacturing (Granulation, Compression, Coating) ensuring compliance with production plans, cGMP, and regulatory standards.

Key Responsibilities

• Execute operations related to granulation, compression, and coating as per Batch Manufacturing Records (BMR) and SOPs.
• Operate, clean, and maintain equipment such as RMG, FBD, tablet press (compression machines), auto coaters, etc.
• Perform line clearance in coordination with QA.
• Ensure in-process checks like weight variation, hardness, thickness, disintegration, friability, etc.
• Maintain all documentation in compliance with GDP (Good Documentation Practices) and Data Integrity.
• Report deviations, breakdowns, and process abnormalities to supervisors.
• Monitor adherence to safety protocols, hygiene, and housekeeping in the manufacturing area.
• Participate in validation and qualification activities (equipment/process).

Skills & Competencies

• Good understanding of cGMP, SOPs, and manufacturing operations.
• Hands-on experience in operating tablet manufacturing equipment.
• Ability to work in shifts and under regulatory-compliant environments.
• Documentation and observation skills.

Qualifications

• B.Pharm / M.Pharm / B.Sc. (Science)
• 2–5 years of relevant experience in regulated pharmaceutical manufacturing (USFDA / MHRA / WHO-GMP).