Quality Assurance assistant
Job Overview
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Date PostedDecember 16, 2024
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Location
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Expiration dateDecember 20, 2024
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Experience3 Year
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QualificationBachelor Degree
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Career LevelOthers
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.