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Executive - Tablet Manufacturing

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Onsite

Executive - Tablet Manufacturing

SAVA HEALTHCARE LIMITED

Executive - Tablet Manufacturing

Skills

Testing & QACompliance

1 year ago

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Important information


Contract type:

Permanent

Location:

Indore, Madhya Pradesh, India

Work mode:

Onsite

Published on:

13 October 2026

What they need


Job highlights

  • Ability to work in shifts and under regulatory-compliant environments
  • Skills Competencies: Good understanding of cGMP,SOPs,and manufacturing operations
  • Maintain all documentation in compliance with GDP (Good Documentation Practices) and Data Integrity
  • Hands-on experience in operating tablet manufacturing equipment

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).

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