Executive - Tablet Manufacturing

SAVA Group; Indore; On-site; INR 600,000 - 1,000,000; Full time

Job summary

SAVA Group is looking for an Executive in Tablet Manufacturing at their Indore facility. The role involves executing and monitoring daily operations, ensuring compliance with production plans, cGMP, and safety protocols. Candidates should possess a B.Pharm, M.Pharm, or B.Sc. in Science, along with 2–5 years in regulated pharma manufacturing. The position requires hands-on experience with tablet manufacturing equipment and the ability to work in shifts in a regulatory-compliant environment.

Qualifications

• 2–5 years of relevant experience in regulated pharmaceutical manufacturing (USFDA / MHRA / WHO‑GMP).
• Hands-on experience in operating tablet manufacturing equipment.
• Ability to work in shifts and under regulatory‑compliant environments.

Responsibilities

• Execute operations related to granulation, compression, and coating as per Batch Manufacturing Records.
• Operate, clean, and maintain equipment such as RMG, FBD, and tablet presses.
• Perform line clearance in coordination with QA.
• Monitor adherence to safety protocols, hygiene, and housekeeping.

Skills

Granulation

Compression

Coating

cGMP

SOPs

Documentation skills

Safety protocols

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).

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).