.
Monitor cleanroom conditions and ensure aseptic practices are followed during injectable production.
2. Documentation & Compliance:
Prepare and maintain accurate production-related documentation like
BMR, logbooks, equipment usage logs, cleaning records
, etc.
Ensure
Good Manufacturing Practices (GMP)
,
Good Documentation Practices (GDP)
, and regulatory norms (e.g., WHO-GMP, USFDA, EU-GMP) are followed.
Participate in
self-inspections, audits
, and implementation of
CAPA
(Corrective and Preventive Actions).
3. Quality & Safety:
Coordinate with QA/QC for
in-process quality checks
, sampling, and line clearance.
Ensure proper
cleaning, sterilization, and validation
of equipment and area before and after batch production.
Identify and report deviations, OOS (Out of Specification), and OOT (Out of Trend) to the QA department.
Follow all
EHS (Environment, Health & Safety)
protocols strictly, including the use of PPE.
4. Inventory & Material Handling:
Monitor and request raw materials, packaging materials, and consumables as per production requirements.
Ensure correct dispensing, usage, and reconciliation of materials.
Maintain inventory of critical spares, tools, and equipment.
5. Team Coordination & Training:
Coordinate with engineering, QA/QC, warehouse, and other departments for smooth production flow.
Guide and supervise operators and workers under the shift.
Participate in training sessions related to
GMP, machine operation, safety
, and
SOPs
.
Job Types: Full-time, Permanent
Pay: ?15,586.79 - ?25,778.31 per month
Benefits:
Food provided
Paid sick time
Paid time off
Provident Fund
Schedule:
Day shift
Work Location: In person
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