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Minimum Requirements Relevant Electrical Draughting qualification or certification . 35 years' relevant electrical drafting experience . Proficiency in AutoCAD . Proficiency in Revit . Good working knowledge of Microsoft Office . Sound understanding of electrical building services . Knowledge of applicable SANS regulations and standards . Ability to read, interpret and work from engineering and architectural drawings. Strong attention to detail and accuracy. Ability to work independently and me…

Electrical Revit Draughtsman

At Imerys, we are committed to fostering a culture of innovation, excellence and professional growth, empowering our employees to reach their full potential. As a global leader in mineral-based specialty solutions operating in more than 40 countries, employing approximately 12,400 individuals worldwide, we offer diverse career opportunities within the mining sector and beyond.Our values are to strive for better, enablers of tomorrow, one team together, partner of choice and every person matters…

Human Resources Intern Centurion, Gauteng

A Vacancy exists for a Cost Accountant in the Technical Division based in Head Office – Centurion The suitable candidate’s main responsibilities and duties include, but are not limited to the following: Basic Function The position is responsible and accountable for delivering the following key outcomes: Ensure financial data integrity across all divisional systems, ensuring data is accurate, complete and reliable for reporting and decision-making. Protect business margins by ensuring the financ…

Cost Accountant

### **Job Context**


Servest is a world class business which is innovative and a leader in the Integrated Facilities Management Industry. The company offers an innovative environment that will accelerate your development and skills, as the highest value is placed on attracting top talent to the organisation.

  



Applications that meet the stated requirements are invited for a vacancy exists for a dynamic and driven **Junior Administrator** to join a team based in Centurion. This role reports directly to the Project Manager at Stats SA.

### **Minimum Requirements**


Qualifications and Experience


* 2 years in accounting / administration environment
* Payroll and / or Health and Safety and / or Human Resource Experience
* Hospitality / restaurant experience
* Management experience
* Relevant Financial Qualification (Business Management, Bookkeeping, Accountancy)
* Basic Computer Literacy – Windows, Outlook, Excel, Word, Internet
* Driver’s License

  



Fundamental Competencies


* Operate a computer
* Ability to work in a multicultural environment
* Provide customer service
* Communicate verbally
* Perform basic accurate calculations
* Prepare written communications
* Maintain health, hygiene and professional appearance


Behaviour Competencies


* Decision Making
* Problem Solving
* Teamwork / Collaboration
* Autonomy and Initiative
* Results Focussed
* Service Focussed
* Communication Skills
* Logical Reasoning
* Analytical Skills
* Resilience and Stress Tolerance
  


Workplace Competencies


* Knowledge, management and application of Company processes and systems
* Working knowledge of Company human resource tools and processes
* Working knowledge of health and safety practices and procedures
* Profit and cost centred
* Business insight
* Knowledge of operational standards and procedures of a business
* Adherence to deadlines


Decision Making


* Operate within the policies and procedures of the Company
* Provide feasible solutions in support of Company requirements

### **Duties \& Responsibilities**

* Comply with relevant legislation
* Behave in accordance with Company vision, values, standards, policies, procedures, code of conduct and disciplinary code
* Practise sound employee relations
* Focus on the customer, both external and internal
* Adhere to the Company dress code
* Comply with standards health, hygiene, safety, security, quality and environmental
* Operationalise service level agreement
* Ensure delivery of a quality administration service
* Adhere to company business processes
* Accurate completion of the required on site book work, e.g., Daily Capturing of invoices, Revenue Analysis, Stock Sheets, Sales Control Sheets, Protein Portion Control, Tie backs, etc.
* Fulfil a general office administration function, e.g. filing, messaging, support resource
* Facilitate the flow of communication, i.e, e\-mails / telephones etc
* Operate within budgetary constraints
* Participate in fire drills and evacuation procedures
* Report incidents and accidents
* Act appropriately in the event of a breach in health, safety and / or security standards / legislation
* Attend meetings and development opportunities
* Perform any other reasonable task(s) required / requested

Junior Administrator

Join us as a **Product Support Technician** where you will provide Level 2 technical support for Collision Avoidance Systems (CAS) and other connected field technologies. This role supports both customers and internal stakeholders by diagnosing and resolving technical issues, analysing device data logs, coordinating warranty evaluations and returns, and assisting with configuration and parameter setups. The technician plays a vital role in ensuring system reliability, product performance, and customer satisfaction across global deployments.

  

**Your Mission:**


* Provide Level 2 technical support to customers, distributors, and internal teams, escalating complex issues when needed.
* Analyse device data logs to identify faults, anomalies, or performance trends.
* Coordinate warranty returns and keep customers informed through the process.
* Support configuration and parameter setup for global teams via remote assistance.
* Record support cases and resolutions in the ticketing system.
* Improve support processes and documentation through feedback and findings.
* Stay current with product updates through regular training.
* Assist with field deployments or remote diagnostics as required.
* Adjust working hours to support teams across time zones.
  

**Your Profile:**


* 3\+ years of experience in technical support, field service, or electronics troubleshooting
* Experience with digital safety systems, industrial automation, or mining technology preferred
* Familiarity with support ticketing systems and customer service workflows
* Diploma or degree in Electrical Engineering, Electronics, Information Technology, or a related technical field.
  

**Location**: Centurion, Gauteng


**Closing Date:** 11 October 2026

  

**Why Epiroc?**


By joining our team, you’ll make a big difference in the energy transition. At Epiroc, we take pride in being passionate innovators, driving the change toward a brighter future for both people and the planet. Guided by our values of Collaboration, Commitment, and Innovation, we foster a culture of trust, growth, and lasting impact.

  

**It all starts with people.** The world needs metals and minerals for the energy transition and our cities and infrastructure must be developed to serve a growing population. To succeed, we need to speed up the shift towards more sustainable mining and construction industries. We at Epiroc accelerate this transformation, together with customers and business partners in more than 150 countries, by developing and providing innovative and safe equipment, digital solutions, and aftermarket support.


All new thinkers are welcome. We are looking for those who want to develop, grow, and dare to think new. In Epiroc we attract, develop, and retain diverse talent valuing authenticity and unique perspectives, driving our spirit of innovation. We foster an inclusive culture where diversity isn't just a goal but a part of our values and way of working. This is how we do business for a sustainable future. Learn more at www.epiroc.com

Product Support Technician

**ADvTECH is the leading provider of private education in Africa, passionately committed to enriching people’s lives and futures. The academic strategy of ADvTECH’s School’s Division is to ensure that each student progresses incrementally toward mastery in a learning environment that is flexible, inspiring, engaging and challenging. ADvTECH houses a number of prestigious school brands offering IEB, Cambridge \& IB curricula and boasts an online home schooling delivery option as well.**  

  

**Duties**  

Foundation phase educators will create a learning experience to stimulate and grow individual talents and equip children with the requisite basic education skills in the areas of reading, literacy and numeracy amongst others. They will need :\-

* to deliver future focused education in which students are motivated, inspired and challenged;
* to demonstrate strength of character, integrity and professionalism, at all times
* to develop and maintain constructive and ongoing partnerships with colleagues, parents, guardians and members of the community
* to communicate and collaborate with all members of the learning community in a positive, respectful and open\-minded way


 They will be accountable for the following specific areas of performance :\-

* Academic Delivery
* Academic Assessment \& Reporting
* Student Behaviour Management
* School Brand Ambassadorship
* Administration
* Health \& Safety

**Qualifications \& Experience**  

* an undergraduate degree (NQF level 6\) in ECD or B. Education (Foundation Phase)
* A PGCE would be necessary if the degree is deemed suitable viz Psychology
* SACE certification and a police clearance are requirements
* 2\-5 years Teaching Experience
* Computer and digital literacy
* First Aid

**Attributes \& Competencies**  

* A Lifelong learner who continually undertakes personal inquiry, reflection and action to inform their practice and understanding of teaching \& learning and remains abreast of global education trends
* Demonstrated planning and organisation skills with superior detail orientation
* Exceptional interpersonal skills with excellent written and verbal abilities and professional presentation skills
* A proven track record of managing professional relationships with maturity and high EQ
* Professional time management is a minimum requirement of the role
* Demonstrated evidence of the ability to think critically and problem solve appropriately

Teacher- Foundation Phase

**Listing reference:** track\_001755
**Listing status:** Online
**Apply by:** 6 October 2026
##### **Position summary**


**Industry:** IT \& Internet
**Job category:** Testing
**Location:** Centurion
**Contract:** Permanent
**Remuneration:** Market Related
**EE position:** Yes
##### **Introduction**


Shape the future of software quality through automation. At Tracker, we're looking for a passionate Analyst: Test Automation to help drive world\-class quality assurance across our Development and Engineering division. If you thrive on solving complex challenges, building robust automated testing solutions, and ensuring exceptional software experiences, this is your opportunity to make a meaningful impact in a fast\-paced technology environment
##### **Job description**


* Collaborate with business stakeholders, development teams, and strategic partners to ensure testing activities align with project objectives and quality expectations.
* Contribute to the definition and implementation of test strategies across multiple projects, ensuring effective communication of testing progress, risks, and outcomes.
* Provide accurate and timely reporting on test execution, quality metrics, and defect trends to support informed decision\-making.
* Foster a collaborative team environment through active participation, constructive feedback, and continuous knowledge sharing.
* Work closely with developers, business analysts, and fellow testers to deliver high\-quality solutions that meet customer and business requirements.
* Support team growth by sharing best practices, lessons learned, and automation expertise.
* Manage end\-to\-end testing activities, including test planning, estimation, execution, monitoring, and reporting across multiple projects.
* Develop and maintain test schedules, resource plans, and effort estimates to ensure successful delivery within agreed timelines.
* Monitor and analyze testing metrics to identify quality trends, risks, and opportunities for process improvement.
* Drive effective defect management practices, ensuring defects are identified, tracked, prioritized, and resolved efficiently.
* Administer and maintain test management tools, repositories, and automation frameworks to support quality assurance objectives.
* Apply industry\-standard testing methodologies, frameworks, and best practices to improve software quality and testing efficiency.
* Demonstrate a high level of professionalism, accountability, and attention to detail in all testing activities.
* Design, develop, and maintain comprehensive test cases, test scripts, and automated test suites based on functional and non\-functional requirements.
* Utilize modern testing and automation tools to enhance test coverage, reduce manual effort, and improve overall quality assurance effectiveness
  

*NB \- This is a 5 days onsite engagement at our centurion office*
##### **Minimum requirements**


* ISTQB – Foundation testing certification (non negotiable).
* Matric (non negotiable)
* ISTQB Advanced Test Analyst is preferable.
* Relevant IT degree or diploma required
* Basic programming knowledge /understanding
* Has training on ReadyAPI, SOAPUI and Visual Studio

**Minimum experience**


* 3 years relevant testing experience (encompassing the skills and knowledge listed below).
* Of the above testing experience should include , writing custom test apps.
* Experience in analysing complex and technical design diagrams and specification.
* Experience in using SQL for Data Driven Testing.
* Experience in API Testing.
* Experience in working with Git repositories and branching strategies.
* Experience in Automated test case development, estimation, and maintenance
* Extensive experience developing test cases and test scenarios from requirements.
* Demonstrates strong analytical and problem\-solving skills and strong attention to detail.
* Possess a good understanding of Quality Control and Quality Assurance concepts across the SDLC.
* Understands test metrics and how they are used for decision support
##### **Benefits**


Provident Fund
Medical aid

Analyst: Test Automation - API

Centurion, South Africa \| Full time \| Home\-based \| R1571281  
Please note that, due to sponsor requirements, we will only consider candidates with experience in MASH, MASLD or Nonalcoholic Steatohepatitis.  


Why Join Global Study Leadership?  


Global Study Leadership is a global, full\-service team delivering clinical trials through both therapeutically aligned and customer\-dedicated delivery models. You'll work across a diverse portfolio including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell \& Gene Therapy, Infectious Disease, Ophthalmology and Women's Health while partnering with leading pharmaceutical and biotechnology sponsors around the world.  


Working alongside experienced project leaders and clinical operations experts, you'll have the opportunity to broaden your therapeutic expertise, strengthen your leadership capabilities and influence the successful delivery of studies that help bring new treatments to patients faster. Supported by a collaborative global network, mentorship, flexible ways of working and AI\-enabled technology and data\-driven insights, you'll be empowered to grow your career while making a meaningful impact on global healthcare.  


What You'll Be Doing  


As a Clinical Lead, you'll be accountable for the clinical delivery of assigned studies, ensuring recruitment, site performance, quality and operational objectives are achieved while maintaining compliance with regulatory requirements and customer expectations.  


Key Responsibilities  


Lead the clinical delivery of regional and global clinical studies, ensuring projects meet quality, timeline, recruitment and operational objectives  
Drive patient recruitment and site engagement strategies, ensuring enrolment targets are achieved and studies remain on track  
Partner with Project Leaders and cross\-functional teams to drive study milestones, resolve issues and maintain operational excellence  
Provide leadership and guidance to clinical teams, supporting resource planning, training and project delivery  
Manage clinical risks, oversee quality standards and drive proactive mitigation strategies throughout the study lifecycle  
Build strong relationships with internal and external stakeholders, ensuring effective communication and alignment across study teams  
Support financial oversight of clinical delivery, including forecasting, budget management and identification of scope changes where applicable  
Contribute to continuous improvement initiatives, knowledge sharing and the development of less experienced team members  
Support proposal development, bid defence activities and clinical delivery planning for new opportunities where appropriate  


What We're Looking For  


Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline  
5\+ years of clinical research, monitoring, or clinical operations experience within a CRO, pharmaceutical, or biotechnology environment  
Strong understanding of clinical trial conduct, ICH\-GCP guidelines and applicable regulatory requirements  
Experience leading clinical study delivery activities, including patient recruitment, site management and clinical quality oversight  
Proven ability to collaborate across cross\-functional teams and manage internal and external stakeholders in a global environment  
Strong communication, problem\-solving, organizational and decision\-making skills  
Experience supporting project financial management and operational planning is desirable  
Passion for advancing clinical research and improving outcomes for patients worldwide  


IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com  


IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.  


Where you'll work  
Home\-based  


You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.  
Culture  


Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Global Study Leadership - Clinical Lead - MASH

The successful candidate will be expected to perform the following duties:

  


**Fleet Management Services**


* Keep BMA fleet in good condition and in a functional state
* To ensure BMA Fleet is Road worthy and licensed at all times
* Coordinate with external service providers for maintenance, repair and services.
* Approval of maintenance authorization for repairs and services
* Facilitate breakdown services
* Monitor and report on vehicle usage and availability.
* Ensure timely and efficient allocation of vehicles to meet organisational needs.
* Schedule and track regular maintenance and repairs for all fleet vehicles.
* Coordinate with external service providers for maintenance and repair services.
* Assist in the Need analysis for procurement of new vehicles and disposal of old ones.


**Administrative Services**


* Updating of weekly vehicle maintenance schedule
* Maintain accurate and up\-to\-date records of all fleet\-related activities, including vehicle registration, insurance
* Maintain records of vehicle maintenance, repairs, and inspections.
* Ensure that Log sheets are controlled and completed for all official trips.
* Booking of vehicle services as per service schedule with various service providers in the different regions and ensuring vehicles are dropped off at the respective service provider and collected thereafter.
* Sending out service notifications to all drivers and managers.
* Assist with stand by functions were officials need to be transported during afterhours.
* Reviewing and updating tracking system reports.
* Checking of monthly tracking system invoices for any discrepancies before processing for payments.
* Co\-ordinate and Communicate with the Suppliers on vehicle matters as reported by the BMA officials.


**Reporting and Compliance**


* Analyse, Prepare and Submitting of Fleet Management monthly invoices for any discrepancies before processing for payments.
* Assist in analysing fleet performance data to identify areas for improvement.
* Managing the administrative process for submitting Traffic Fines representations on behalf of the driver or organization if a fine is contested. Handling the payment or redirection of fines (Section 56 notices or summons) to the driver, often coordinating with Port Commanders.
* Preparing reports on fleet Performance, including fuel usage and vehicle maintenance schedules.
* Conduct regular inspection of facilities for adherence to standards and protocols and recommend corrective actions and set work priorities.
* Investigation of accidents/Incidents involving BMA vehicle.
* Prepare a report on the accident to be submitted to the Loss Control Committee
* Record Keeping: Maintaining a database of traffic offenses, fines paid, and driver misconduct records to monitor trends and enforce driver accountability
* Attend to all Audit matter as and when required.


**Personnel Management and Relations**


* Supervise and manage fleet management administrative staff
* Formulate and review performance plans for administrative staff
* Process personnel leave applications on time
* Build and maintain relationships with all BMA officers including Governance Committees for the purposes of expectations management and knowledge sharing.
* Progress and challenges in achieving the operational plans to impacted stakeholders.

  

**Requirements**


**Minimum qualifications**



Grade 12 (Matric)



Three years Degree at (NQF 7\) in Transport/Logistic management / Public Administration or Public Management.



Fleet management will be an added advantage.


**Other requirements**


* Flexibility in working hours will be required to meet demands of the role.
* May be required to work overtime.
* Valid driver’s License.
* PrDP will be an added advantage.


**Minimum experience**


* Minimum 4 years supervisory experience within Transport/Fleet management.


**Knowledge**


* South African Constitution Act, 1996
* Border Management Authority Act, 2020
* Public Finance Management Act (The PFMA) and Treasury Regulations
* National Road Traffic Act of 1996 No 93
* The Constitution of RSA, 1996\.
* AARTO Act, Act 46 of 1998
* National Travel Policy Travel Framework ACT 1997
* National Treasury Guidelines and Instructions Notes
* Other relevant legislations that regulate the use of vehicles.
* Government Motor Transport Handbook


The BMA is an equal opportunity employer committed to employment equity and workforce diversity preference may be given to suitably qualified candidates from designated groups in line with the BMA employment equity plan. The BMA reserves the right not to make an appointment to the advertised positions.


* It is the applicant’s responsibility to have all foreign qualifications evaluated by South African Qualification Authority (SAQA), confirm the appropriate NQF level and to provide proof of such evaluation report.
* Shortlisted candidates may be subjected to an **interview** and **technical assessment(s)** (which assesses the candidate's demonstrated professional and technical competency against the job requirements and duties).
* Candidates potentially considered suitable after the interview and technical test(s) for senior positions, will be subjected to a competency assessment (which tests the candidate's demonstrated proficiency in the professional dimensions attached to the level of the post);
* Employment suitability checks will be conducted on the shortlisted candidates (credit, criminal, citizenship, employment references and qualification verifications);
* Appointments will be subjected to a mandatory vetting/security clearance appropriate to the level of the position.


**NB: This position is being re\-advertised, and candidates who previously applied are encouraged to reapply should they still be interested in the position.**



Closing date: 12 October 2026

OFFICER: FLEET MANAGEMENT

Declaration
The South African Weather Service (SAWS) is a Section 3(a) public entity under the Ministry of Water and Environmental Affairs and is governed by a Board of Directors. The company became a public entity on 15 July 2001 in terms of the South African Weather Service Act (No. 8 of 2001\). It is an authoritative voice for weather and climate forecasting in South Africa and as a member of the World Meteorological Organization (WMO) it complies with international meteorological standards.

  

  

As an Aviation Meteorological Authority, SAWS is designated by the state to provide weather services to the aviation industry, marine and a range of other identified clients and to fulfil a range of international obligations of the government of South Africa. SAWS is also the official provider of weather and climate information for the South African public and for commerce.


  
Logistics Officer (Technical services)
To coordinate and provide effective logistics and supply support services to SAWS Technical Services, including inventory and warehouse management, asset and stock control, logistics coordination, in support of infrastructure maintenance and operational service delivery. The role is responsible for maintaining accurate logistics records, ensuring the availability and control of required materials and assets, coordinating logistics activities with internal and external stakeholders, and ensuring compliance with applicable SCM, PFMA, health and safety, and organisational requirements.


**Reference \#:** WS05/092026
  

Centurion / Irene
  

**Closing date:** 09 Oct 2026 23:59

Logistics Officer (Technical services)

**Job Description – FINANCIAL ACCOUNTANT**

**Key Competencies \& requirements:**

* 3 to 5 Years experience in Financial management
* BCom Degree in Accounting \- COMPULSORY
* Membership at SAIPA or SAICA
* Syspro experience will be an added advantage
* Established proficiency in MS Office with emphasis on Excel
* Good interpersonal skills and ability to communicate effectively
* Availability to work extended hours as per operational requirements
* Passionate about getting things done right, first time \& every time
* Ability to work efficiently, on own or as part of a team, in a highly pressurized environment
* Excellent sense of urgency, sound business and financial acumen

**Key Functions of Role, BUT NOT LIMITED TO:**

* Full accounting function
* Full processing from source documents to trial balance
* Preparation and processing of monthly journals, salary journals, depreciation journals, Interest on loan accounts etc.
* General ledger account reconciliations
* Full Processing of cash book and reconciliation
* Debtors and Creditors control account reconciliation and processing
* Bank Reconciliations
* Monthly VAT Calculations and VAT Recons
* Preparation of Monthly Intercompany Invoices
* Preparation of Monthly Management Reports and Accounts
* Preparation of Annual Financial Statements and assist with audit and queries.
* Calculation of Corporate Income Tax
* SARS e\-filing submission and administration and liaise with SARS for any queries.
* Manage Loans
* Manage and prepare monthly costs by Projects.
* Filing on Annual Returns
* EMP501 and EMP201
* IT14 – tax returns
* Admin Duties
* Financial Reporting
* Profit Forecasting
* Budget Planning and preparation
* GL Reconciliation
* Cash Book Management
* Banking and bank payments
* Insurance portfolio
* FAR

Financial Accountant

Centurion, South Africa \| Full time \| Home\-based \| R1571276  
Due to sponsor requirements, only candidates with a strong Oncology background will be considered for the role  


Why Join Global Study Leadership?  


Global Study Leadership is a global, full\-service team delivering clinical trials through both therapeutically aligned and customer\-dedicated delivery models. You'll work across a diverse portfolio including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell \& Gene Therapy, Infectious Disease, Ophthalmology and Women's Health while partnering with leading pharmaceutical and biotechnology sponsors around the world.  


Working alongside experienced project leaders and clinical operations experts, you'll have the opportunity to broaden your therapeutic expertise, strengthen your leadership capabilities and influence the successful delivery of studies that help bring new treatments to patients faster. Supported by a collaborative global network, mentorship, flexible ways of working and AI\-enabled technology and data\-driven insights, you'll be empowered to grow your career while making a meaningful impact on global healthcare.  


What You'll Be Doing  


As a Clinical Lead, you'll be accountable for the clinical delivery of assigned studies, ensuring recruitment, site performance, quality and operational objectives are achieved while maintaining compliance with regulatory requirements and customer expectations.  


Key Responsibilities  


Lead the clinical delivery of regional and global clinical studies, ensuring projects meet quality, timeline, recruitment and operational objectives  
Drive patient recruitment and site engagement strategies, ensuring enrolment targets are achieved and studies remain on track  
Partner with Project Leaders and cross\-functional teams to drive study milestones, resolve issues and maintain operational excellence  
Provide leadership and guidance to clinical teams, supporting resource planning, training and project delivery  
Manage clinical risks, oversee quality standards and drive proactive mitigation strategies throughout the study lifecycle  
Build strong relationships with internal and external stakeholders, ensuring effective communication and alignment across study teams  
Support financial oversight of clinical delivery, including forecasting, budget management and identification of scope changes where applicable  
Contribute to continuous improvement initiatives, knowledge sharing and the development of less experienced team members  
Support proposal development, bid defence activities and clinical delivery planning for new opportunities where appropriate  


What We're Looking For  


Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline  
Strong Oncology background  
5\+ years of clinical research, monitoring, or clinical operations experience within a CRO, pharmaceutical, or biotechnology environment  
Strong understanding of clinical trial conduct, ICH\-GCP guidelines and applicable regulatory requirements  
Experience leading clinical study delivery activities, including patient recruitment, site management and clinical quality oversight  
Proven ability to collaborate across cross\-functional teams and manage internal and external stakeholders in a global environment  
Strong communication, problem\-solving, organizational and decision\-making skills  
Experience supporting project financial management and operational planning is desirable  
Passion for advancing clinical research and improving outcomes for patients worldwide  


IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com  


IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.  


Where you'll work  
Home\-based  


You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.  
Culture  


Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Global Study Leadership - Clinical Lead - Oncology

Centurion, South Africa \| Full time \| Hybrid \| R1570557  
Job Overview  


Act as a stand\-alone global functional lead at a project level applying experience, knowledge and expertise for Safety Aggregate Report and Analytics (SARA) Center deliverables including but not limited to safety aggregate reports, literature surveillance, signal management activities and benefit risk management documents. Actively contribute to Lifecycle Safety global process initiatives and work in close collaboration with the safety customer delivery management team regarding project/client initiatives. Ensure team is following standard best\-in\-class practices established by the SARA infrastructure.  


Essential Functions  


* Serve as a stand\-alone global lead for aggregate reporting, signal management, or literature surveillance projects.
* Lead, author and finalize aggregate reports, including but not limited to PBRERs/PSURs, DSURs, PADERs, RMPs, REMS, ACOs, line listings
* and author responses to regulatory agency/ Pharmacovigilance Risk Assessment Committee (PRAC) inquiries, as required.
* Act as literature lead, back\-up lead, reviewer/QCers to conduct ongoing literature safety surveillance for marketed and investigational products. Assist with the identification of ICSRs from literature, evaluation of events of special interests as well as aggregate data \&/or signal detection relevance review. Author and/or contribute to literature deliverables for aggregate reports \&/or signal management activities meeting strict regulatory timelines.
* Act as Signal Management Lead on large and/or complex post\-marketing and clinical trial projects. Set\-up, implement, organize (including documentation) and lead safety management teams. Serve as subject matter expert across projects for complex data mining methodologies and algorithms on internal and external safety data sources. Oversee/set\-up and update products' signaling strategies. Oversee/author and/or QC review all types of signal management deliverables.
* Oversee/conduct ongoing signal detection activities as per agreed signaling strategies, perform signal validation and signal evaluation analyses for proactive and timely identification of signals and characterisation of risks . Accountable for full documentation and tracking of signals. At project level, maintain compliance, prepare metrics and KPI, present at audits and inspections.
* In a PV support role, act as functional lead and oversee/author and/or QC review safety responses to regulatory agencies/PRAC and justification documents to support labelling documents.
* Provide training to SARA staff for qualification on SARA deliverables
* May perform quality check of all assigned SARA deliverables
* be responsible for the quality of the final SARA deliverable to client regulatory, IQVIA regulatory reporting (RR), and regulatory authorities.
* Provide consultative guidance to internal and external stakeholders in the for all SARA deliverables.
* Act as mentor to and coach to project team staff and direct line reports.
* Interface with clients and other functional groups within Lifecycle Safety and other business units, such as Regulatory affairs Reporting (RR), Real World Late Phase (RWLP), Medical Writing, Clinical Research, Quality, Knowledge Quality Management (KQM), Pharmacovigilance Support (PVS), Project Leads (PL), Medical Safety Advisors (MSA), Qualified Persons for Pharmacovigilance (QPPV) / Pharmacovigilance Contact at National Level (PCNL), Library Information Services (LIS), Safety Operations (SO), Business development (BD) and Proposals, and Information Technology (IT), as needed
* Participate in internal and external audits, as required. Lead audit preparation activities in advance to audit and ensure audit readiness of project
* Review project files and contact lists on a regular basis to ensure compliance with SOPs
* Lead functional team and contribute to achievement of departmental goals e.g. utilization realization and productivity metrics.
* Read and acknowledge all necessary IQVIA standard operating procedures (SOPs) and customer SOPs as required. Ensure all required training is executed in a timely fashion and documented. Ensure Good Documentation Practices (GDP).
* Serve as the interface between the global project lead and the working team
* conduct regular lessons learnt with the working teams to ensure all information from the customer is cascaded to the relevant team members.
* Provide mentorship and training to less experienced resources.
* Provide regular reports to overall project manager and department management on project metrics, statement of work (SOW) changes, client requests or concerns
* participate in project review meetings with management
* communicate and document project issues to project team members and department management in a timely manner.
* Contribute to resource needs and resource allocation based on workload to ensure appropriate compliance with report submissions.
* Build a positive, collaborative team environment with SARA team members, lead by example and provide training and mentoring for local project leads and less experienced team members.
* Contribute and assist in global/local working groups as applicable in implementation of new operational initiatives, identification and implementation of process efficiencies.
* Participate in the review of existing standard operating procedures (SOPs).
* Proactively identify issues and propose solutions.
* Provide consultative guidance to internal and external stakeholders for all SARA deliverables.
* Suggest, drive, and implement continuous process improvements across all SARA center services.
* Collaborate with line managers to resolve project performance related issues of staff.

Qualifications  


Life science graduate/post\-graduate, pharmacy, nursing, or other healthcare related qualification or experience in pharmacovigilance  
5\-10 years of relevant experience in Pharmacovigilance including hands\-on experience of drug safety, aggregate reports, signal detection/signal management preferred  
Excellent communication (written and verbal) skills  
Strong organizational and time management skills. Proven ability to meet strict deadlines  
Manage competing priorities and ability to be flexible and receptive to changing demands  
English – fluent (spoken, written)  


IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com  


IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.  


Where you'll work  
Hybrid  


You’ll split your time between home and the office, giving you the flexibility to focus where you work best while still building strong in\-person connections with your team. This model combines the autonomy of remote work with the collaboration, energy and resources of an office environment.  
Culture  


Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best 

Safety Aggreg Report Mng /Senior PV Scientist

Centurion, South Africa \| Full time \| Home\-based \| R1571249  
Associate Site Activation Manager (Study Start Up) – Global Study Leadership  


At IQVIA, our Associate Site Activation Managers play a critical role in bringing innovative medicines to patients faster. You'll lead global study start\-up and site activation activities, partnering with sponsors, investigative sites and cross\-functional teams to accelerate patient enrolment, drive successful study execution and influence site activation strategy across complex regional and global clinical trials. This is an opportunity to make a direct impact on study timelines and patient outcomes while working with some of the world's leading pharmaceutical and biotechnology companies.  


Why Join Global Study Leadership?  


Global Study Leadership is a global, full\-service team delivering clinical trials through both therapeutically aligned and customer\-dedicated delivery models. You'll have the opportunity to support studies across a diverse portfolio including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell \& Gene Therapy, Infectious Disease, Ophthalmology and Women's Health while partnering with leading pharmaceutical and biotechnology sponsors worldwide.  


Working alongside experienced project leaders and global study teams, you'll help shape site activation strategies, navigate complex regulatory environments and deliver innovative solutions that support successful study delivery. Supported by a collaborative global network, mentorship, flexible ways of working and AI\-enabled technology and data\-driven insights, you'll have exceptional opportunities to broaden your expertise, expand your leadership impact and accelerate your career within one of the world's leading clinical research organizations.  


What You'll Be Doing  


As a key member of the project leadership team, you'll be responsible for the successful delivery of site activation activities across regional, multi\-regional and global studies, ensuring regulatory, contractual, quality, timeline and customer objectives are achieved.  


Key Responsibilities  


Lead site activation activities from study award through site activation, ensuring studies are positioned for successful patient enrolment and on\-time delivery  
Develop and execute Site Activation Management Plans aligned to study strategy, scope, timelines and customer requirements  
Partner with sponsors, sites and cross\-functional teams to drive study start\-up, regulatory submissions, ethics approvals, contracting and country activation activities  
Provide strategic guidance on regulatory requirements, submission strategies and site activation approaches across diverse global markets  
Manage study timelines, risks, budgets, scope and operational performance, proactively identifying and resolving critical path challenges  
Build strong relationships with sponsors and investigative sites, delivering an exceptional customer experience and fostering long\-term partnerships  
Drive issue resolution, stakeholder alignment and decision\-making across countries and regions to ensure successful study execution  
Support bid defence activities, proposal development and study start\-up strategy discussions for new business opportunities  
Mentor and support colleagues, contribute to process improvements and champion operational excellence across Global Study Leadership  


What We're Looking For  


Bachelor's degree in Life Sciences, Healthcare, or a related scientific discipline  
3\+ years of experience in site activation, study start\-up, regulatory affairs, clinical operations, or a related clinical research environment  
Experience leading regional, multi\-country, or global site activation activities within a CRO, pharmaceutical, or biotechnology environment  
Strong knowledge of clinical trial regulations, ICH\-GCP guidelines, ethics submissions, site activation processes and clinical trial agreements  
Proven success managing study timelines, risks, quality, budgets and operational performance across complex studies  
Demonstrated ability to build trusted sponsor and site relationships and effectively manage stakeholders in a global environment  
Strong negotiation, communication, leadership, problem\-solving and project management skills  
Ability to navigate complex regulatory environments and deliver innovative solutions that accelerate study start\-up  
Passion for advancing clinical research and helping bring life\-changing therapies to patients worldwide  


Build Your Future with IQVIA  


If you're looking for a role that combines global study start\-up leadership, strategic sponsor partnership, operational excellence and meaningful impact, we'd love to hear from you. At IQVIA, you'll have the opportunity to work on high\-profile global clinical trials, collaborate with industry\-leading sponsors, leverage innovative technologies and build a rewarding career within a global organization dedicated to transforming healthcare and improving patient outcomes worldwide. Working on some of the industry's most complex studies, you'll help accelerate study start\-up, enable patient enrolment and play a vital role in bringing new treatments to patients faster.  


IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com  


IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.  


Where you'll work  
Home\-based  


You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role.  
Culture  


Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers.

Associate Site Activation Manager

Our well\-known client within the **Fast Food Franchising Sector**, based in Centurion, is looking for a **Junior Bookkeeper** to join their team!
**Requirements:**  

* Grade 12 (Matric)
* Tertiary qualification: Certificate, Diploma or degree in financial management.
* 2 \- 4 years of commercial bookkeeping experience.
* Must have experience taking books up to trial balance.
* Experience in a multi\-store franchise, or retail environment is strongly preferred.


  

**System knowledge:**  

* Sage Evolution
* Intermediate Excel and Google sheets


  

**Key Responsibilities:**  

* Full function Bookkeeping to trial balance (Portfolio of 6\-11 stores).
* Compile, verify and process monthly journals and invoicing across all revenue streams (Cahs, credit and, Online, Mr D and Uber Eats).
* Import bank statements into cashbooks and perform weekly ban reconciliations against Sage Evolution.
* Process stock journals, call account entries, salary allocations, depreciation, and bookkeeping service fee invoices.

  

  

For more information please contact:
Nadine Mundy

Junior Bookkeeper

Lovisa is fast\-fashion Retail  

Lovisa is global, and its growth is infectiously energetic  

See us at careers.lovisa.com

**Fixed\-term Festive contract**

**To be considered, you will need to be available throughout November, December, and early January,** ***including Black Friday, Day of Reconciliation, Christmas Eve, Christmas Day, Day of Goodwill (26 December), New Year's Eve, and New Year's Day.***

**Interviews will be held from mid\-October, over a number of weeks.**


First day of work is **Monday, 16 November 2026**


The contract continues until **Sunday, 03 January 2027**

**Benefits**

* Top\-notch training to become a great Team Member (and piercing training!)
* First\-rate Store and Regional Manager to draw support
* Team Referral Rewards Program
* Product for you to wear in\-store from our top\-fashion ranges
* Funky, on\-trend customers
* Bright, warm store
* Easy to explain product
* Oh, and a generous discount on our jewellery!

**Job Description**

* You will live for fashion
* Sell with great customer experience
* Conduct our Piercing service
* Replenish sold stock on the move
* Manage the register
* Clean up the store at open and close
* Build great relationships with colleagues and customers
* Be yourself! Enjoy yourself!

**About you:**

* Strong desire to help and guide customers
* A drive to deliver great results
* An eye for fashion and are aware on all the latest trends
* Strong performance in a face\-to\-face customer environment

*We believe in supporting diverse cultures and harnessing the unique knowledge and experience of our team. We celebrate our global presence, by supporting our culturally diverse team around the world.*

Team Member - Part time - Festive Fixed Term

Our well\-known client within the **Fast Food Franchising Sector**, based in Centurion, is looking for an **Entry Level Finance Clerk** to join their team!
**Education \& Qualifications:**  

* Grade 12 (Matric) with Accounting or Maths essential.

**Experience and track record:**  

* No previous experience is required however if would be advantageous.

**Key Responsibilities:**  

* Capture daily store cash\-ups onto master accounting sheets via Google Drive Shop reports.
* Verify physical paperwork against declared cash\-ups.
* Process credit card slips into bank modules or spreadsheet logs.
* Perform transactional bank reconciliations and immediately flag/escalate cash discrepancies.
For more information please contact:
Nadine Mundy

Entry Level - Finance Clerk

You would be responsible for meeting the support requirements of our clients, in a way that respects the individual and promotes their independence. You would be expected to travel to the client's home and assist them with daily tasks as agreed between the client and Charlton Kings . For more information call or whatsapp 067 627 3077. The type of support that you would be providing is no different to what would reasonably be given by a member of the person's family. For instance, you may be pro…

Nursing Assistant/Carer

Join Shoprite as a Facilities Co\-Ordinator in Centurion, Gauteng, where you will expertly manage contractor activities, monitor maintenance schedules, and ensure compliance with Occupational Health and Safety (OHS) standards within a dynamic distribution centre environment. This full\-time role requires proven experience in facilities management, contractor coordination, budget control, and equipment maintenance, with a strong focus on material handling equipment (MHE) and safe workplace enforcement.

Facilities Co-Ordinator

Optimi is looking for individuals with exceptional communication and administration skills to join the Administration and Academic Services team as Temporary Program Administration Agent (Quality Assurer). The ideal candidates should be results orientated, committed to meeting deadlines, and able to work well within a team. REQUIREMENTS Grade 12. A minimum of 2 years experience in a similar role. Familiarity with Microsoft Office and Google Chrome. Proficiency in English both verbally and in wr…

Temporary Program Administration Agent

Optimi is currently seeking a well-organised individual with a people-oriented approach to join our team as an Education Specialist for Technology 7-9 and Engineering Graphics and Design Grades 10-12. The ideal candidate should have a positive outlook, be adaptable to change and excel as a team player with exceptional communication skills. It is essential that the candidate have an in-depth understanding of all CAPS requirements and can critically evaluate content within the subject field. REQU…

Education Specialist: Technology, Engineering Graphics and Design

Optimi is looking for a dedicated and customer-orientated individual to join the Client Engagement team as a Helpdesk Consultant. The ideal candidates should be deadline-driven with strong solution development abilities and excellent communication skills and can analyse and resolve queries. REQUIREMENTS Grade 12 Certificate in Client Support, Customer Service, or a related field (Advantageous) 1- 3 years Client Support / Call centre experience preferably with technical support Experience with Z…

Helpdesk Consultant

We are looking for an experienced Parts & Logistics Manager to join a dynamic automotive organisation and take responsibility for parts pricing, inventory optimisation, dealer support, logistics efficiency and accessory development. The successful candidate will play a key role in ensuring the right parts are available at the right time, while supporting dealer operations, improving stock turnover and maintaining accurate parts catalogues and pricing structures. Key Responsibilities Manage and …

Parts & Logistics Manager

Join the Polished Team

**Polished** is looking for a passionate, skilled, and experienced **Somatologist/Beauty Therapist** to join our growing team. If you are dedicated to helping clients look and feel their best while delivering exceptional service, we would love to hear from you.

**Start Date: 1 October 2026**

Position: Experienced Somatologist

**Location:** Midstream, Centurion  
**Employment Type:** Full\-Time

Key Responsibilities

* Perform a variety of facial treatments tailored to clients' skin concerns and needs.
* Provide professional body and facial waxing services.
* Apply classic, hybrid, and volume eyelash extensions.
* Conduct relaxing and therapeutic massages.
* Perform eyebrow shaping, tinting, and lash tinting services.
* Recommend suitable skincare and aftercare products.
* Maintain high standards of hygiene, cleanliness, and client care.
* Build and maintain strong relationships with clients.
* Ensure treatment rooms are prepared and stocked at all times.
* Assist with retail sales and promotion of salon services.

Minimum Requirements

* Qualified Somatology/Beauty Therapy certification.
* Minimum 2 years' experience in a salon, spa, or aesthetic environment.
* Proven experience in:
* Eyelash extensions
* Body and facial waxing
* Facials and skincare treatments
* Massages
* Brow and lash treatments
* Excellent customer service and communication skills.
* Professional appearance and positive attitude.
* Ability to work weekends and flexible hours when required.
* Reliable, punctual, and self\-motivated.

Advantageous Skills

* Chemical peels
* Microneedling
* Makeup application
* Advanced skincare knowledge
* Retail sales experience
* Existing client base

What We Offer

* Competitive salary plus commission opportunities
* A modern, professional, and supportive work environment
* Opportunities for growth and development
* The chance to be part of an exciting and expanding beauty brand

How to Apply

Interested candidates should send their CV, qualifications, and a portfolio or photographs of their work to Polishedmidstream@gmail.com

**Applications close: 30 September 2026**

*Join Polished and help our clients look and feel their absolute best through exceptional beauty and wellness treatments.*

Pay: R3 750,00 \- R28 597,66 per month

Work Location: In person

Jobs in Centurion - Page 4

Vacancies (page 4 of 8)