Cleaning of Vacuum Cleaner

Cleaning of  Vacuum Cleaner

Objective

  • To lay down a procedure for the cleaning of Vacuum Cleaner.

Scope

  • This SOP is applicable for cleaning of Vacuum Cleaner to warehouse of formulation plant

Responsibility

  • Operator / Technician – For cleaning of Vacuum Cleaner.
  • Warehouse personnel– For checking the cleanliness of the equipment.

Accountability

  • Department Head/incharge & QA Head shall be accountable for implementation of this SOP.

Abbreviations and Definitions

  • QA                              :            Quality Assurance
  • WH                             :            Warehouse
  • RM                              :            Raw Material
  • SOP                             :            Standard Operating Procedure

Procedure

Cleaning of  Vacuum Cleaner

Procedure for cleaning of Vacuum Cleaner

  • Switch OFF the vacuum cleaner.
  • Remove “Status” label and affix ‘To be cleaned’ label.
  • Dismantle the parts (cover with gasket, Hose pipe and Filter bag) and take it to equipment wash room.
  • Remove the Powder collected in Filter bag in poly bag and destroy as per SOP.
  • Mop the vacuum cleaner with wet duster then with dry duster.
  • Mop the dismantled parts and body of vacuum cleaner using wet dusters then with dry duster except filter bag.
  • Assemble the dismantled parts to vacuum cleaner.
  • Remove “TO BE CLEANED” label and affix the “CLEANED” label.

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Forms and Records (Annexures)

  • Not Applicable.

Distribution

  • Master copy          –           Quality Assurance
  • Controlled copies         –            Quality Assurance, Raw Material Store.

History

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About Alice

Alice is the Author and founder of Drugsformulations, she is a pharmaceutical professional having more than 18 years of rich experience in pharmaceutical field. During her career, she works in the quality assurance department with multinational companies i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, and Nectar life Science Ltd. During his experience, she faces many regulatorily audits i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda, Kenya, Tanzania, Zimbabwe. She is currently leading a regulatory pharmaceutical company as a Head Quality. You can join him by Email, Facebook, Google+, Twitter, and YouTube

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