Full job description
BIOVAC is one of the main sterile vaccine producers rooted in Africa, with our core cause being to “protect life”. We are searching to appoint a dynamic, passionate, confident, proactive and meticulous Quality Assurance Graduate (Fixed Term Contract -24 Months) to be a part of a goal-oriented team.

Purpose of the role:

Assist line supervisor and crew individuals to supply enter and aid operational practices.
Assist with imparting stakeholders with on-going remarks till profitable completion of duties or projects.
Ensure compliance in accordance with the Related Substances Act a hundred and one of 1965 and the Pharmacy Act fifty three of 1974, and the corporations policies, strategies and different relevant laws
Partner, aid and assist the place requested, crew contributors to make sure sufficient teamwork and success of crew deliverables.
Continuously assist and prescribe to cGMP inside Biovac.
Be section of a dynamic rotational software designed to supply publicity and ride in the areas of Quality, Quality Assurance, Validation, Training and Quality Control.
Ensure that the things to do related with Quality structures in the Quality Assurance Department supply offerings and options in alignment with pharmaceutical exceptional machine necessities and cGMP
Plan and function Quality Assurance features at the excellent requirements (SA GMP, PIC/S and WHO) to make sure that merchandise are of the best required for their supposed use
QUALIFICATIONS NEEDED:

Degree /Diploma in applicable subject of study.
KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

Duties and Responsibilities Duties & Responsibilities

Routine Activities

Assist line supervisor with particular tasks, consisting of however now not restricted to research, facts taking pictures and working intently with one-of-a-kind group contributors to research extra about the company.
Understands the average thinking of the company, such as the brand, customer, product desires and all different elements of service.
Rotates thru the crew to obtain publicity to specific accountability and presents thoughts to develop and enhance the manner inside specified departments.
Accepts designated, business-focus tasks to research, recommend thoughts and solutions, and current closing mission throughout internship.
Provides guidelines to administration for enhancing inner processes.
Learns and will become knowledgeable on inner software program system.
Participate in a structured rotational program, gaining hands-on journey in Quality Assurance, Training, Validation, and Quality Control.
Work carefully with cross-functional groups to apprehend and make a contribution to a variety of elements of the best administration process
Undertake difficult initiatives each six months, working underneath the mentorship of the Head of the department, Managers and Technical experts
Collaborate with crew individuals to efficaciously execute and supply tasks on time.
Assist in growing and enforcing fantastic systems, policies, and procedures.
Participate in the validation of equipment, processes, and structures in accordance with enterprise standards.
Perform danger assessments and validation protocols to make certain product pleasant and safety..
Contribute to the execution of best manage activities, inclusive of trying out and inspection of uncooked materials, in-process, and completed products.
Analyze records and collaborate with applicable groups to tackle exceptional issues
Assist Supervisor with things to do with the eQMS platforms, this consists of closure of Trackwise tickets raised
Monitor eQMS dashboards and check trends. Work with method proprietors to proactively improve damaging developments with the Quality system.
Monitor goal dates and work with departments to actively shut QMS objects inside goal dates for all QMS structures (Deviation, Incident, CAPA, Actions, Risk assessments, SOPs).
Support supervisor with constructing and going for walks nearby coaching program.
Drive non-stop enchancment motion plans to decrease the variety of deviations, incidents and CAPAs on site
Write technical reviews to analyse CAPAs, deviations, Incident tendencies and furnish non-stop improvements
Create computerized reviews to help website online in proactively enticing QMS items, and as required through stakeholders.
Provide records enter for APQRs from the eQMS and assessment and analyse records even as makings conclusions
Supporting Quality Management

Building very own cGMP understanding and compliance
Participate in attaining the companys first-rate objectives.
Participate in constructing a sustainable first-rate tradition on website and proactive mitigate dangers that might also negatively influence high-quality or expand these appropriately.
Ensuring audit readiness inside very own position via closing out audit findings timeously
Ensure Deviations, Change Controls, CAPAs are treated effectively
Advocate non-stop improvement.
Application Deadline: five December 2025

If you do no longer acquire a response from us inside three weeks after closing date please recognize that your utility was once now not successful.

Disclaimer:

Dear Applicant, we recognize your hobby in becoming a member of our organization. It is necessary for us that you apprehend how we manage your information. We are dedicated to making sure the protection and confidentiality of the data you provide. Your private small print will be accrued for the sole motive of the software method and will be used strictly for that purpose. By applying, you renowned and consent to the collection, use, and safety of your non-public data in accordance with our privateness policy. If you have any inquiries or concerns, our Human Capital branch is on hand to furnish clarification. We seem ahead to reviewing your application.

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