SOP for Operating Filling Machines – V 2.0

Procedure for Operating Filling Machines

Department	Production/Engineering/Quality Assurance (QA)
SOP No.	SOP/Ointment/043
Supersedes	V 1.0
Page No.	Page X of Y
Issue Date	[Insert Issue Date]
Effective Date	[Insert Effective Date]
Review Date	[Insert Review Date]

1. Purpose

The purpose of this Standard Operating Procedure (SOP) is to establish a systematic process for operating filling machines during ointment production. Proper operation ensures accurate filling, minimizes wastage, and maintains product integrity.

2. Scope

This SOP applies to all personnel involved in handling, operating, and maintaining filling machines in the ointment manufacturing facility.

3. Responsibilities

Production Supervisor: Ensures filling operations comply with batch requirements.
Machine Operator: Operates and monitors the filling machine.
Quality Assurance (QA) Personnel: Conducts in-process checks to confirm filling accuracy.
Engineering Technician: Maintains and calibrates the filling machine.

4. Accountability

The Production and QA Managers are accountable for ensuring that the filling operation follows GMP standards and is properly documented.

5. Procedure

5.1 Pre-Operational Checks

Ensure the filling machine is clean and sanitized.
Verify the calibration of volume control settings.
Check that all connections, hoses, and nozzles are securely attached.
Ensure that the batch is approved for filling.

5.2 Loading the Product into the Filling Machine

Transfer the ointment from the storage tank to the hopper.
Ensure the transfer is done under controlled conditions to prevent contamination.
Maintain the product at the required temperature for proper flowability.

5.3

Setting Up the Machine for Filling

Adjust the volume settings as per batch specifications.
Set the speed and pressure to ensure uniform filling.
Run a test fill to confirm accuracy before starting full-scale production.

5.4 Filling Process

Start the filling machine and monitor the initial output.
Ensure that each container is filled to the correct volume.
Check for leaks, air bubbles, or uneven filling.
Maintain a steady pace to prevent fluctuations in filling levels.

5.5 Monitoring During Filling

Conduct periodic weight checks to ensure consistency.
Monitor for any signs of nozzle clogging or product overflow.
Ensure the temperature remains within the specified range.

5.6 Completion of Filling

Stop the machine after the last batch is filled.
Check all filled containers for uniformity.
Record the batch details and verify compliance before sealing.

5.7 Cleaning and Shutdown

Flush the filling machine with an approved cleaning solution.
Sanitize all contact surfaces to prevent cross-contamination.
Document the cleaning process in the Equipment Cleaning Log.

6. Abbreviations

GMP – Good Manufacturing Practices
QA – Quality Assurance
QC – Quality Control
RPM – Revolutions Per Minute
BMR – Batch Manufacturing Record

7. Documents

Filling Log (Annexure-1)
Equipment Cleaning Log (Annexure-2)

8. References

WHO GMP Guidelines for Pharmaceutical Manufacturing
21 CFR Part 211 – Current Good Manufacturing Practices
Equipment Manufacturer Guidelines

9. SOP Version

Version 2.0

10. Approval Section

	Prepared By	Checked By	Approved By
Signature
Date
Name
Designation
Department

11. Annexures

Annexure-1: Filling Log

Date	Batch Number	Container Size (g/ml)	Target Volume	Actual Volume	Verified By
01/02/2025	SOP/Ointment/001	50g	50g	50.2g	QA Officer
02/02/2025	SOP/Ointment/002	100g	100g	99.8g	QA Officer

Annexure-2: Equipment Cleaning Log

Date	Filling Machine ID	Cleaning Agent Used	Sanitization Method	Verified By
01/02/2025	FM-101	Sodium Hypochlorite	Rinsed and Dried	QA Head
02/02/2025	FM-102	Ethyl Alcohol	Wiped and Flushed	QA Head

12. Revision History:

Revision Date	Revision No.	Details of Revision	Reason for Revision	Approved By
01/01/2024	1.0	Initial Version	New SOP	QA Head
01/02/2025	2.0	Updated SOP Format	Standardization of Document	QA Head