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Job Safety Analysis for Tablet Compression Machine

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Job Safety Analysis for Tablet Compression Machine

JSA for Safe Operation of Tablet Compression Machine

JSA Number JSA/OralDosage/001/2025 Department Oral Dosage
Revision Number V 1.0 Issue Date 01/02/2025
Effective Date 05/02/2025 Review Date 05/02/2026

1. Purpose

The purpose of this JSA is to identify and mitigate potential hazards associated with the operation of the Tablet Compression Machine used in the production of solid oral dosage forms.

2. Scope

This JSA applies to all operators, maintenance personnel, and supervisors involved in using, cleaning, and maintaining the Tablet Compression Machine in the Oral Dosage department.

3. Responsibilities

Operators:

  • Ensure the machine is operated per SOPs.
  • Wear appropriate Personal Protective Equipment (PPE).
  • Report any malfunctions or safety concerns immediately.
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Supervisors:

  • Ensure compliance with safety guidelines.
  • Monitor risk control measures and address safety violations.

Safety Officers:

  • Conduct regular safety audits.
  • Provide training on hazard mitigation and emergency response.

4. Definitions & Abbreviations

  • PPE: Personal Protective Equipment (e.g., gloves, goggles, ear protection).
  • LOTO: Lockout/Tagout – Procedure to isolate hazardous energy.
  • Risk Assessment: A process to evaluate and control hazards.

5. Procedure

Step Task Description Potential Hazard Risk Level (L/M/H) Control Measures
1 Machine setup and calibration Pinching, crushing injuries High Use guards, follow SOP
2 Loading raw materials Dust exposure, inhalation Medium Wear dust mask and gloves
3 Compression operation Mechanical failure, noise exposure High Regular maintenance, use ear protection
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6. Risk Assessment

Likelihood Consequence Risk Level
Rare Minor injury Low
Possible Noise-induced
hearing loss
Medium
Likely Severe injury from machine failure High

7. Emergency Procedures

  1. In case of injury, seek medical assistance immediately.
  2. If a mechanical failure occurs, stop operation and inform maintenance.
  3. For dust exposure incidents, move to fresh air and use eyewash if needed.
  4. All incidents must be reported and logged.

8. Required PPE & Safety Controls

  • Safety gloves: Protect hands from crushing and sharp edges.
  • Ear protection: Prevents hearing damage due to noise exposure.
  • Face mask: Reduces inhalation of dust particles.
  • Safety goggles: Protects against dust and debris.
  • Machine guard: Must always be in place during operation.

9. References

  • OSHA 1910.212 – Machine Guarding Standards.
  • ISO 45001 – Occupational Health & Safety Standards.
  • Manufacturer’s Operation Manual for Tablet Compression Machine.

10. Approval Section

Name Designation Signature Date
[Name] Prepared By
[Name] Checked By
[Name] Approved By

11. Revision History

Version Date Description of Changes Approved By
V 1.0 01/02/2025 Initial Release [Name]
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Oral Dosage Forms (Tablets & Capsules) Tags:Pharmaceutical Hazard Analysis, Pharmaceutical Job Safety Analysis, Pharmaceutical Risk Assessment, Pharmaceutical Safety Analysis, Pharmaceutical Safety Assessment, Pharmaceutical Safety Audit Checklist, Pharmaceutical Safety Audits, Pharmaceutical Safety Checklist Template, Pharmaceutical Safety Checklists, Pharmaceutical Safety Compliance, Pharmaceutical Safety Documentation, Pharmaceutical Safety Evaluation, Pharmaceutical Safety Guidelines, Pharmaceutical Safety Inspection Checklist, Pharmaceutical Safety Inspections, Pharmaceutical Safety Management, Pharmaceutical Safety Measures, Pharmaceutical Safety Monitoring, Pharmaceutical Safety Plans, Pharmaceutical Safety Policies, Pharmaceutical Safety Procedures, Pharmaceutical Safety Procedures Manual, Pharmaceutical Safety Programs, Pharmaceutical Safety Protocols, Pharmaceutical Safety Regulations, Pharmaceutical Safety Review, Pharmaceutical Safety Risk Assessment, Pharmaceutical Safety SOPs, Pharmaceutical Safety Standards, Pharmaceutical Safety Training

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Standard Operating Procedures V 1.0

  • Aerosols
  • Analytical Method Development
  • Bioequivalence Bioavailability Study
  • Capsule Formulation
  • Clinical Studies
  • Creams
  • Data Integrity
  • Dental Dosage Forms
  • Drug Discovery
  • Environment, Health and Safety
  • Formulation Development
  • Gels
  • Good Distribution Practice
  • Good Warehousing Practices
  • In-Process Control
  • Injectables
  • Liquid Orals
  • Liposome and Emulsion Formulations
  • Lotions
  • Lyophilized Products
  • Maintenance Dept.
  • Medical Devices
  • Metered-Dose Inhaler
  • Microbiology Testing
  • Nanoparticle Formulation
  • Nasal Spray Formulations
  • Nebulizers
  • Ocular (Eye) Dosage Forms
  • Ointments
  • Otic (Ear) Dosage Forms
  • Pharmacovigilance
  • Powder & Granules
  • Purchase Departments
  • Quality Assurance
  • Quality Control
  • Raw Material Stores
  • Regulatory Affairs
  • Tablet Manufacturing
  • Rectal Dosage Forms
  • Transdermal Patches
  • Vaginal Dosage Forms
  • Validations and Qualifications

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NEW! Revised SOPs – V 2.0

  • Aerosols V 2.0
  • Analytical Method Development V 2.0
  • API Manufacturing V 2.0
  • BA-BE Studies V 2.0
  • Biosimilars V 2.0
  • Capsules V 2.0
  • Creams V 2.0
  • Elixers V 2.0
  • Ointments V 2.0
  • Raw Material Warehouse V 2.0
  • Tablet Manufacturing V2.0

New Publication: A must for All.

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