Quality Assurance assistant

December 16, 2024

Job Overview

  • Date Posted
    December 16, 2024
  • Location
  • Expiration date
    December 20, 2024
  • Experience
    3 Year
  • Qualification
    Bachelor Degree
  • Career Level
    Others

Job Description

Assist in for quality management systems, control and documentation.

Key Responsibilities

  • Assist in determining training needs, train cGMP and monitoring of compliance with requirements of cGMP.
  • Assist in documentation and evaluation BMRs and BPRs.
  • Assist Reviewing, developing of missing SOPs and implementation of SOPs.
  • Handle product related customer complaints as well as execute and co-ordinate product recalls, together with supporting staff.
  • Convene self-inspections and/or quality audits and make recommendations, where applicable.
  • Assist in ensuring that all requisite validations are carried out.
  • Investigate and set standards for quality and health and safety.
  • Ensuring manufacturing processes comply with standards at both national and international level.
  • Ensuring maintenance of his/her Department, premises and equipment.
    • Carry out vendor audits.
    • Assist in Preparation of training and self-inspection schedules.
    • Specify quality requirements of raw and packaging materials with suppliers.
  • Ensure initial and continual training of Departmental Personnel as necessary.
    • Ensure appropriate manufacturing systems in-process controls are implemented.
  • Review and authorize/reject any document that gives work instructions and set requirements such as procedures, protocols, test methods, and specifications—including changes to these documents.
  • Review and authorize/reject production batch records and make the final decision to release a product lot into commerce.
  • Ensure investigation is conducted and root cause is eliminated for production and control record errors, discrepancies, and failure to meet specification, including quality attributes.
  • Review complaints to determine if it relates to a failure to meet specification, if so investigate and report to regulatory authorities if serious and unexpected.
  • Be independent reviewer and authorizer with respect to manufacturing and process/ product development units.
  • Establish Quality procedures and standards.
  • Authorize written procedures and other documents.
  • Control and archiving of records and documents.
  • Prepare Corrective actions and preventive action (CAPA) records.
  • Retrieval and filling of complete BMRs and BPRs

How to Apply

Send CV to vacancies@jantakenya.com by 20th December 2024.