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SOP for Training of Manufacturing Personnel

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SOP for Training of Manufacturing Personnel

Standard Operating Procedure for Training of Manufacturing Personnel

1) Purpose

The purpose of this SOP is to establish procedures for the training of manufacturing personnel to ensure they are qualified and competent to perform their assigned tasks.

2) Scope

This SOP applies to all personnel involved in the training process for the production of intramuscular, subcutaneous, and intravenous injection products.

3) Responsibilities

The responsibilities of this SOP include:
– Training Coordinator: Organizing and scheduling training sessions.
– Supervisors/Managers: Ensuring personnel are trained and competent to perform their tasks.
– Quality Assurance (QA) Department: Reviewing and approving training materials and records.

See also  Injectables: SOP for Media Fill Validation

4) Procedure

4.1 Training Needs Assessment
4.1.1 Identify training needs based on job roles and responsibilities.
4.1.2 Develop a training plan that includes required training sessions, materials, and schedules.
4.2 Development of Training Materials
4.2.1 Create training materials that cover the necessary knowledge and skills for each job role.
4.2.2 Ensure training materials are reviewed and approved by the QA department.
4.3 Conducting Training Sessions
4.3.1 Schedule training sessions and notify personnel of their training requirements.
4.3.2 Conduct training sessions using approved materials and methods.
4.3.3 Provide hands-on training and practical demonstrations where applicable.
4.4 Evaluation of Training
4.4.1 Assess the effectiveness of

training through tests, practical evaluations, or assessments.
4.4.2 Provide feedback to trainees and offer additional training if necessary.
4.5 Documentation of Training
4.5.1 Maintain records of all training sessions, including the date, participants, and topics covered.
4.5.2 Ensure training records are signed and dated by the trainer and trainee.
4.6 Ongoing Training and Competency
4.6.1 Implement ongoing training programs to ensure personnel maintain and update their skills.
4.6.2 Reassess and retrain personnel as needed based on performance evaluations or process changes.

See also  SOP for Change Control in Manufacturing Processes

5) Abbreviations, if any

– QA: Quality Assurance

6) Documents, if any

– Training Plans
– Training Materials
– Training Records

7) Reference, if any

– Good Manufacturing Practices (GMP) Guidelines
– International Organization for Standardization (ISO) Standards

8) SOP Version

Version 1.0

Injectables Tags:Analytical method validation for injections, Aseptic media fill trials SOP, Bioburden testing for injections, Cleaning validation for injection equipment, Emulsion stability testing for injections, Formulation development for injections, Homogeneity testing for injections, IM injection SOP, Injection filling volume accuracy, Injection stability testing, Intramuscular injection procedure, Intravenous injection guidelines, IV injection SOP, Needle assembly for syringes SOP, Packaging integrity testing for injections, Particle size analysis for injections, Pre-filled syringe stability testing, Product sterility in aseptic processing, Reconstitution testing for injections, SC injection SOP, Subcutaneous injection technique, Syringe filling and capping SOP, Syringe labeling and inspection SOP, Temperature mapping in storage areas, Viscosity testing for injections

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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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