sop for Scrap Management
1.0 Objective
To lay down a procedure for handling and transfer the scrap from various departments to the scrap yard.
2.0 Scope
This Standard Operating Procedure is applicable for handling and transfer the scrap from various
departments to the scrap yard to be followed at formulation plants of abc Pvt. Ltd.
3.0 Responsibility
3.1 Officer / Executive concerned department shall be responsible for handling and transfer of scrap to scrap yard.
3.2 Officer / Executive QA shall be responsible for verification of scrap before transfer to scrap yard.
3.3 Officer / Executive HR Department shall be responsible for verification and shall receive the scraps in scrap yard.
3.4 Concerned department head and Head QA shall be responsible for compliance this SOP.
4.0 Abbreviations and Definitions
SOP : Standard Operating Procedure
QA : Quality Assurance
QC : Quality Control
No. : Number
NRR : Non Recoverable Rejects
HR : Human Resource Department
5.0 Procedure
5.1 Different type of scrap is generated in the plant. This scrap shall include empty
containers, gunny bags, plastic and rubber scrap, used polythene bags / used disposable
hand gloves / shoe covers / nose masks / lint free cloth, paper waste, waste of
corrugated box, stationary / carton / label, waste of broken ware, rejected glass
bottles, rejected blister / strips, NRR generated from capsule, QC department
and general waste generated in the plant.
5.2 Empty fiber container of raw materials / plastic container / empty reagent bottles:
5.2.1 Cross mark the empty containers / plastic containers by permanent marker
pen as ‘X’. Deface the labels of empty bottles. Rinse the bottles with water.
Collect them in a waste bin and label it as per Annexure-1.
5.2.2 Transfer scrap to the designated place of common scrap collection point
after recording the details in scrap transfer form (Annexure-2).
5.3 Empty Gunny Bags: Empty gunny bags of raw material are counted by warehouse and
the details are recorded in scrap transfer form and send to scrap collection point.
5.4 Plastic scrap / rubber scrap / used polythene bags / used disposable hand gloves / shoe covers / nose masks / lint free cloth:
5.4.1 Collect the scrap mentioned above in a polythene bag.
5.4.2 Affix the label after recording the details (Annexure-1).
5.4.3 Enter the details in scrap transfer (Annexure-2).
5.4.4 Transfer the bags to common scrap collection point.
5.5 Corrugated box / paper waste / stationary / carton waste into several parts and collect in a polythene bag.
5.5.1 Tear the waste / rejected corrugated boxes, paper waste into several parts and collect in a polythene bag.
5.5.2 Affix the label and record the details in scrap transfer note.
5.5.3 Transfer the bags to common scrap collection point.
5.6 Broken glass bottles
5.6.1 Collect the scrap containing broken glass of bottles from production area take out wash
with water and allow the water to drain by flushing after neutralization in designated area.
5.6.2 Collect it in a polythene bag. Affix the label and record its details in scrap transfer form.
5.6.3 Transfer the bag to common scrap collection point.
5.7 Rejected empty strips / blister
5.7.1 Collect the empty blister / strip, pieces of foils in a polythene bag after the defoiling procedure.
5.7.2 Affix the status label as per Annexure-1 on the bag and enter the details in scrap transfer
form (Annexure-2) and send to scrap collection point.
5.8 Non recoverable rejects generated from tablet and capsule department
5.8.1 Waste generated during in-process or in filling, sealing and packing operation, shall be
treated by taking out its liquid from filled bottle in a separate container and discard through Destruction Form.
5.8.2 Bottles and ROPP Caps shall be discarded through Scrap Form affixed with Scrap label.
5.9 Non-recoverable rejects generated from QC laboratories
5.9.1 First deface or destroy the label on sample poly bag after testing of capsules, raw material taken for
observation or conducting physical test in QC are treated as NRR are soaked in water in a plastic container.
5.9.2 Liquid waste like solution taken for analysis shall drained in sink by flushing with water.
5.9.3 Collect broken glassware & empty reagent bottles in a polythene bag. Affix the label after recording
the details. Enter the details in scrap transfer form and transfer them to scrap yard.
5.9.4 General waste generated in the plant
5.9.5 Collect all the general waste & segregate all the items like old slippers, torn booties, waste of lint free
cloth in a polythene bag. Transfer these bags to the scrap yard after recording the details
5.10 Scrap containing expired chemicals / reagent / solvent
5.11 After all the scrap is transferred to the scrap collection point, the responsible person in this area shall
check the scrap for following
5.11.1 All the Containers / Bottles / Labels shall be defaced.
5.11.2 No product or usable printed packaging (coated & uncoated) material is in scrap.
5.11.3 Segregate the bags containing scrap received as per the nature of the material as mentioned below
5.11.3.1 Glass
5.11.3.2 Plastic
5.11.3.3 Foil
5.11.3.4 Papers and others
5.11.3.5 Rejected strip / blister
5.12 After complete verification of the scrap, the person from Personnel & Administration
Department (HR) weighs the above segregated scrap and records its weight in Scrap Transfer Form.
5.13 Transfer the scrap from the collection point to common Scrap Yard and keep it till its disposal.
5.14 The scrap containing empty Blister / Strip shall be Shredded by means of Shredder / Crushing
Machine and filled in the bag and placed at designated place till its disposal.
5.15 Annexure -2 is the duplicate logbook one copy is HR department and second copy is initiator department.
5.16 Incase any filled Bottle / Strip / Blister / Coated / Uncoated / Printed Label found in scrap,
Scrap Yard person shall immediately inform to concern person / HR Department / QA Department.
6.0 Forms and Records
6.1 Scrap Label – Annexure-1
6.2 Scrap Transfer Form – Annexure-2
7.0 Distribution
7.1 Master copy – Documentation Cell (Quality Assurance)
7.2 Controlled copies – Quality Assurance, Quality Control, Production
Warehouse, Personnel & Administration.
8.0 History
| Revision Number | Details For Change |
Reason for Revision |
| 00 | New SOP | NA |
- process validation protocol for methylcobalamin niacinamide and pyridoxine injection
validation protocol of sterility test
sop for Analytical Method Transfer
Protocol for hold time study of sterile garments
sop for swab sampling for validation of clean surfaces
cleaning validation maco and noel calculation formula
sop for performance qualification for analyst
Sop for Validation report for disinfectant efficacy
Sop for Method validation report for bacterial endotoxin test
Sop for method validation microbiology sterility testing
sop for validation report for preservative efficacy test
sop for Protocol cum report for efficacy qualification of uv light
sop for validation protocol for uv light efficacy of dpb & laf
sop for cleaning validation protocol tablet manufacturing equipment
sop for cleaning validation protocol ointment manufacturing equipmentconcurrent process validation for rabeprazole ec and domperidone sr capsules
sop for Validation for cleaning procedure liquid injection
sop for Validation for cleaning procedure dry powder injection
Preparation Approval Control and Distribution of Master Formula Records
calibration policy for equipment and instruments
evaluation Sampling of Raw Materials questionnaire
training evaluation questionnaire
sop for approval of Contract Parties
sop for Operation and Cleaning of Purified Water Generation System
sop for Storage of Standard Weights
-
process validation protocol for methylcobalamin niacinamide and pyridoxine injection
validation protocol of sterility test
sop for Analytical Method Transfer
Protocol for hold time study of sterile garments
sop for swab sampling for validation of clean surfaces
cleaning validation maco and noel calculation formula
sop for performance qualification for analyst
Sop for Validation report for disinfectant efficacy
Sop for Method validation report for bacterial endotoxin test
Sop for method validation microbiology sterility testing
sop for validation report for preservative efficacy test
sop for Protocol cum report for efficacy qualification of uv light
sop for validation protocol for uv light efficacy of dpb & laf
sop for cleaning validation protocol tablet manufacturing equipment
sop for cleaning validation protocol ointment manufacturing equipmentconcurrent process validation for rabeprazole ec and domperidone sr capsules
sop for Validation for cleaning procedure liquid injection
sop for Validation for cleaning procedure dry powder injection
Preparation Approval Control and Distribution of Master Formula Records
calibration policy for equipment and instruments
evaluation Sampling of Raw Materials questionnaire
training evaluation questionnaire
sop for approval of Contract Parties
sop for Operation and Cleaning of Purified Water Generation System
sop for Storage of Standard Weights
sop for Verification of Weighing Balance
-
Sop for Submitting of Leave Application
sop for Accident Management Procedures
sop for Accident Management Procedures
Cleaning and colour coding of Factory Apparel (Clothes)
Job Responsibilities of Key Personnel
sop for Maintenance of Building
Destruction of Batch Production and Control Records BPCR
Procedure for Sampling of Rinse water Swab
Cleaning Validation of Equipment
Measurement and Recording of Temperature and Relative Humid
Sampling of Product at Intermediate Stages
Approval of Overprinting on Packing Material
sop for Procedure for Reprocessing
Preparation and Control of Master Batch Production and Control record
Issuance and Retrieval of Control documents
Calibration Policy for equipment
procedure for batch numbering system for products
sop for Handling of Incident during operation
Procedure for Allocation of Numbers for Machine Equipment
Validation and Qualification Facility System and Equipment
In-process Checks During Packing Operation
Operation and Calibration of Leak Test Apparatus
Operation and Calibration of Friability Tester
