BIOVAC is one of the leading sterile vaccine manufacturers rooted in Africa with our core purpose being to protect life. We are looking to hire a dynamic passionate confident proactive and meticulous 3X- Validation Technician to join a goal-oriented team.
QUALIFICATIONS NEEDED:
- Completed qualification within any field of Natural/Health Sciences/ Engineering.
NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:
- Experienced in writing of technical documents.
- Basic experience in testing and troubleshooting practices.
- At least 6 months in a qualification / validation role within the pharmaceutical industry.
KEY DUTIES & RESPONSIBILITIES OF THE ROLE:
Core Technical Delivery:
- Liaising with service providers.
- Participate in Process Development activities.
- Execution of validation processes: PD PV CV CSV Mapping Cold Chain Facility Decontamination Periodic Reviews and Periodic Revalidations as per defined timelines and according to cGMP
- Assist equipment owners with identifying maintenance and calibration requirements.
- Participates in troubleshooting a wide range of problems which require creative thinking. Exercises significant technical discretion in design execution and interpretation and pursues new validation/qualifications studies as a result of experimental outcomes.
- Communication status and any delays/ issues/ changes experienced during validation.
- Communicate with departments regarding validation planning and time needed on validation activities.
- Provide guidance to staff from other departments regarding the required content of procedures.
- Manage internal customer relations and communication.
- Ensure relevant OOS and OOT investigation non-conformances/ deviations change controls and CAPAs are initiated and completed to the correct standard.
- Identify quality risks in the section and initiate risk management where required e.g. to support investigation or choices.
Application Deadline: 21 November 2025
If you do not receive a response from us within three weeks of submitting your application please understand that your application was not successful.
We believe in the magic of diversity within teams and to achieve this we do apply Employment Equity principles during our selection process where this is necessary to achieve such diversity.
Disclaimer:
Dear Applicant we appreciate your interest in joining our organization. It is imperative for us that you understand how we handle your information. We are committed to ensuring the security and confidentiality of the information you provide. Your personal details will be collected for the sole purpose of the application process and will be used strictly for that purpose. By applying you acknowledge and consent to the collection use and protection of your personal information in accordance with our privacy policy. If you have any inquiries or concerns our Human Capital department is available to provide clarification. We look forward to reviewing your application.
BIOVAC is one of the leading sterile vaccine manufacturers rooted in Africa with our core purpose being to protect life. We are looking to hire a dynamic passionate confident proactive and meticulous 3X- Validation Technician to join a goal-oriented team. QUALIFICATIONS NEEDED: Completed qualificati...
BIOVAC is one of the leading sterile vaccine manufacturers rooted in Africa with our core purpose being to protect life. We are looking to hire a dynamic passionate confident proactive and meticulous 3X- Validation Technician to join a goal-oriented team.
QUALIFICATIONS NEEDED:
- Completed qualification within any field of Natural/Health Sciences/ Engineering.
NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:
- Experienced in writing of technical documents.
- Basic experience in testing and troubleshooting practices.
- At least 6 months in a qualification / validation role within the pharmaceutical industry.
KEY DUTIES & RESPONSIBILITIES OF THE ROLE:
Core Technical Delivery:
- Liaising with service providers.
- Participate in Process Development activities.
- Execution of validation processes: PD PV CV CSV Mapping Cold Chain Facility Decontamination Periodic Reviews and Periodic Revalidations as per defined timelines and according to cGMP
- Assist equipment owners with identifying maintenance and calibration requirements.
- Participates in troubleshooting a wide range of problems which require creative thinking. Exercises significant technical discretion in design execution and interpretation and pursues new validation/qualifications studies as a result of experimental outcomes.
- Communication status and any delays/ issues/ changes experienced during validation.
- Communicate with departments regarding validation planning and time needed on validation activities.
- Provide guidance to staff from other departments regarding the required content of procedures.
- Manage internal customer relations and communication.
- Ensure relevant OOS and OOT investigation non-conformances/ deviations change controls and CAPAs are initiated and completed to the correct standard.
- Identify quality risks in the section and initiate risk management where required e.g. to support investigation or choices.
Application Deadline: 21 November 2025
If you do not receive a response from us within three weeks of submitting your application please understand that your application was not successful.
We believe in the magic of diversity within teams and to achieve this we do apply Employment Equity principles during our selection process where this is necessary to achieve such diversity.
Disclaimer:
Dear Applicant we appreciate your interest in joining our organization. It is imperative for us that you understand how we handle your information. We are committed to ensuring the security and confidentiality of the information you provide. Your personal details will be collected for the sole purpose of the application process and will be used strictly for that purpose. By applying you acknowledge and consent to the collection use and protection of your personal information in accordance with our privacy policy. If you have any inquiries or concerns our Human Capital department is available to provide clarification. We look forward to reviewing your application.
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