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  • Posted: Nov 26, 2025
    Deadline: Dec 31, 2025
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  • Biovac was founded in 2003 to revive and restore South Africas vaccine manufacturing capabilities. We are an African based manufacturer contributing towards filling the gap that exists in the lack of African vaccine manufacturing capability. We recognise that well only achieve this if we match scientific innovation through local biotechnology skills with ...
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    Data Integrity Lead

    • 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 Data Integrity Lead to join a goal-oriented team.

    QUALIFICATIONS NEEDED:

    • Degree or Diploma in Computer Science, Information Technology, Information Systems, Engineering, Automation or related discipline.

    NECESSARY EXPERIENCE & INDUSTRY KNOWLEDGE:

    • 3-5 years of experience in a pharmaceutical or biotechnology environment with a focus on qualification and validation specifically CSV, data integrity, quality assurance, or regulatory compliance.
    • Strong understanding of regulatory requirements and guidelines related to CSV and data integrity (e.g., FDA CFR Part 11, Annex 11, GAMP).
    • Experience with electronic document management systems (EDMS), laboratory information management systems (LIMS), and other electronic data capture systems.
    • Excellent analytical skills and attention to detail, with the ability to identify issues, analyse root causes, and implement effective solutions.
    • Strong communication and interpersonal skills, with the ability to effectively collaborate with cross-functional teams and communicate complex concepts to diverse audiences.

    KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

    Core Technical Delivery:

    • Liaising with internal and external service providers.
    • Define general DI and CSV activities and the associated strategy.
    • Ensure execution of all DI and CSV activities according to the defined schedules.
    • Define CSV and DI qualification approaches to new equipment for site.
    • Ensure execution of Qualification processes: DQ, Impact Assessment, IQ and OQ as defined timelines in accordance with GAMP guidance.
    • Assist system owners with identifying information maintenance requirements.
    • Participate in and lead troubleshooting discussions to investigate a wide range of challenges which require creative thinking.
    • General administration such as updating of the master plan / validation plan, maintaining schedules, standard referencing of documentation.
    • Exercise significant technical discretion in design, execution, and interpretation, and pursues new studies as a result of experimental outcomes.
    • Communicate DI and CSV status to the business on a regular basis.
    • Communicate any delays/ issues/ changes experienced during DI and CSV task execution.
    • Communicate with departments related to DI and CSV activity planning and allocated timelines.
    • Provide guidance to staff from other departments related to the required content of procedures.
    • Identify quality risks in the section and initiate risk management where required, e.g. to support investigation decisions.
    • Provides scientific input into problems and new initiatives to ensure that a science & risk-based approach is adoptive to support.
    • Ensure that SOPs, Plans and documents are up to date with the latest pharmaceutical and best practice guidelines.
    • Ensure Deviations, Incidents, Change Controls, CAPAs, audit findings, RAs related to DI and CSV are handled effectively.
    • Ensure that the DI and CSV schedule are in place, communicated, updated and delivered on according to defined timelines.
    • Support the Validation Manager with DI and CSV strategy and associated department goals setting.
    • Provide guidance and oversight for activities performed by external stakeholders according to defined schedules.
    • Lead significant investigations linked to DI and CSV activities.

    Application Deadline: 29 November 2025

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    Senior Finance Systems Analyst

    • 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 Senior Finance Systems Analyst to join a goal-oriented team

    QUALIFICATIONS NEEDED:

    Required:

    • Bachelors degree or diploma in Financial Accounting or equivalent.

    Preferred:

    CA(SA) or CIMA
    Experience needed to deliver the role seamlessly:

    • Bachelors degree in Finance, Accounting, or related field; professional accounting qualification (e.g., CA, CIMA) preferred.
    • 5 -7 years of SAP FI/CO experience, including at least one full-cycle implementation in a manufacturing or pharmaceutical environment.
    • Strong understanding of production costing, inventory valuation, and financial integration with PP/MM.
    • Experience in regulated industries with knowledge of compliance frameworks (e.g. GMP).
    • Excellent communication, stakeholder management, and project leadership skills.
    • Experience with SAP FI/CO, Fiori apps, and reporting tools.
    • SAP S/4HANA Finance experience.

    KEY DUTIES & RESPONSIBILITIES OF THE ROLE:

    Core Technical Delivery:

    Finance & Controlling (FI/CO)

    • Define and champion core FI/CO business processes, including leading cross-functional efforts to identify and prioritize enhancements that align SAP FI/CO capabilities with finance strategy and operational efficiency.
    • Oversee end-to-end business process improvements for SAP FI/CO modules, guiding requirements gathering and validation to ensure they meet evolving finance needs and drive measurable business value.
    • Design and implement and maintain core CO functionalities including:
    • Cost Centre Accounting
    • Internal Orders
    • Profit Centre Accounting
    • Product Costing and Cost Object Controlling
    • Actual vs. Plan variance analysis
    • Month-end closing processes and allocations
    • Ensure accurate integration of FI/CO with other modules such as MM, SD, and PP.
    • Support financial reporting, compliance, and audit readiness in line with industry regulations (e.g., GMP).

    Production Planning & MRP Integration

    • Collaborate with Information Technology (IT), Production Planning (PP) and Supply Chain teams to ensure seamless integration between FI/CO and PP/MM modules.
    • Direct the business requirements for product cost planning, cost estimates, and production order costing, collaborating with stakeholders to establish policies and workflows that optimize cost accuracy and profitability.
    • Lead the design and implementation of product cost planning, cost estimates, and production order costing.
    • Establish and enforce business rules for financial treatment of MRP-driven procurement and inventory transactions, partnering with IT to validate that system outputs reflect accurate financial reporting and compliance.
    • Support Material Ledger setup and actual costing processes for accurate inventory valuation.
    • Drive the financial aspects of batch costing, production variances, and settlement processes.

    Sales & Distribution (SD) Integration

    • Partner with commercial and supply chain teams to ensure financial integration of SD processes with FI/CO.
    • Provide business expertise and validation for SD-related financial flows, including defining key integration points, success criteria, and ongoing monitoring to support revenue recognition and billing processes:
    • Customer invoicing and revenue recognition
    • Credit management and billing
    • Integration of sales orders with profitability analysis (CO-PA)
    • Tax determination and posting
    • Inter-company sales and stock transfers
    • Ensure accurate posting of revenue, cost of goods sold (COGS), and customer receivables.
    • Validate pricing procedures and their impact on financial postings.
    • Assist in designing controls for order-to-cash processes in compliance with pharmaceutical industry standards

    Project Leadership & Stakeholder Engagement

    • Facilitate fit-gap analysis, blueprinting, and solution design workshops with cross-functional stakeholders.
    • Project management of FI/CO enhancements of change requests ensure that user requirements are scoped, co-ordinate UAT and ensure that changes work as intended post implementation.
    • Lead data migration efforts for finance and controlling master and transactional data.
    • Develop and deliver training for finance and operations users, support change management initiatives.
    • Provide post-go-live support and drive continuous improvement across finance and production processes.

    Additional Duties

    • Business Planning Actively involved in the business planning and forecasting activities
    • Management Business and financial reporting
    • KPI tracking and adherence
    • Product Costing & Reporting
    • Business Intelligence/Insights reporting

    Application Deadline: 31 December 2025

    Method of Application

    Use the link(s) below to apply on company website.

     

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