1,173 South Africa jobs in South Africa

Our client, a dynamic organization in the private sector, is seeking a meticulous and experienced Auditor to join their team in Johannesburg / Western Cape . As the Auditor, you will play a vital role in maintaining accurate financial records and ensuring compliance with regulatory requirements. This position offers an excellent opportunity to contribute significantly to the financial success of the organization.

• Meticulous attention to detail
• Strong analytical skills
• Excellent communication and interpersonal skills
• Ability to work independently and as part of a team
• Proven track record of meeting deadlines and managing multiple tasks simultaneously
• Proficiency in accounting software such as Pastel/Zero
• Proficiency in Microsoft Excel and Word
• Valid driver's license

Software Requirements:

• CaseWare, Pastel Partner, Sage, Proficiency in Pastel/Zero, Excel, Word, and Microsoft Office suite

Educational Requirements:

• Completion of SAICA/SAIPA Articles
• BCom Accounting Degree with or without honours or similar qualification

R20 000 - R40 000

Join our dynamic team and contribute to our ongoing success in delivering top-quality products and services to our valued customers. Apply now through pnet or submit the following to :

• Updated CV
• Qualifications (does not need to be certified) must include a full record of All University marks, a degree certificate, or letter from university confirming that you have fulfilled all requirements for the degree
• A professional head and shoulders photo of yourself

Launched in 2000, Business Accounting Network (BAN) is the first accounting franchise in South Africa, servicing the small and medium-sized business sector.

We are constantly looking for talented professional and chartered accountants nationwide, who want to start their own accounting business but find it daunting to resign from the comfort and secure salary of their current job.

If you are talented, hard-working, disciplined, and want to shine at your own accounting practice at home, but aren’t sure you can drum up clients and handle the non-billable pressure to stay ahead technically, then this is your chance.

We’re an established, well-known national network of professionals with a reputation for excellence who will provide you with client referrals, technical support, and training as you set up your own practice using your SAIPA/SAICA articles or 5+ years of accounting and tax experience. On your own, but not alone!

You can expect to earn between R60,000 to R80,000.

• Auditing/Accounting

Concor Construction invites suitably qualified candidates to apply for the position of HSE Practitioner to join our projects across Southern Africa. The successful incumbent will be responsible for ensuring compliance with statutory requirements related to occupational health, safety, and environmental legislation. Preference will be given to Employment Equity candidates.

Key Responsibilities

• Identify hazards and associated risks through daily inspections.
• Implement and maintain Concor and Client health, safety, and environmental requirements on the project.
• Facilitate hazard identification and risk assessment sessions.
• Assist in incident investigations and verify corrective and preventative action plans.
• Contribute to the reduction of safety risks and environmental impacts.
• Ensure legal compliance of contractors on sites.
• Ensure all safety equipment required by law is available on site, maintained in good order, and kept in its proper place.
• Conduct internal audits and liaise with external auditors.
• Keep accurate records of HSE statistics.
• Adhere to agreed policies, processes, standards, procedures, protocols, and documentation at all times.
• Implement and maintain HSE management systems.

Qualifications

• SAMTRAC or equivalent.
• Registered as a construction health & safety officer with SACPCMP.
• Incident Investigation certification.
• Fall Protection Planner certification.

Experience

• A minimum of 3 years’ experience as a Health & Safety Officer within the construction industry, with preference given to candidates with experience in the construction and buildings sector.
• Valid driver’s licence.
• South African citizenship.

Knowledge and Skills

• Advanced knowledge of Microsoft Office (Excel, PowerPoint, Word & Outlook).
• Working knowledge of the OHS Act and Construction Regulations .
• Experience conducting inspections and completing inspection registers and checklists.
• Good interpersonal and communication skills.

A mobile-first services platform is looking for a Frontend Architect to assist and contribute to their platform that handles millions of transactions.

This merit-based, delivery-focused team of high performers with diverse skills and backgrounds works closely with payment, content, and other integration partners from all over the world.

They are looking for an Architect Developer who can conceptualize and decompose software in terms of its capabilities, features, and components.

1. 10+ years of experience
2. Unit testing experience with TDD
3. Azure experience is beneficial

Remote role - so you can work anywhere in SA.

We have a current opportunity for an Architect Developer Web Apps on a permanent basis. The position will be based in Cape Town. For further information about this position please apply.

We have an amazing opportunity for a Tailings Engineer based in South Africa .

Level: Experienced

Key Requirements:

1. Bachelor's degree in Engineering or related field.
2. Minimum of 5 years of experience in tailings engineering within the mining industry.
3. Professional Engineer (PrEng) certification preferred.
4. In-depth knowledge of tailings management principles, practices, and regulations.
5. Proficiency in tailings dam design, construction, and monitoring.
6. Experience in conducting geotechnical investigations and analyses related to tailings facilities.
7. Familiarity with relevant software for geotechnical analysis and modeling.
8. Strong understanding of environmental regulations and best practices related to tailings management.
9. Ability to collaborate effectively with multidisciplinary teams, including geotechnical engineers, environmental specialists, and regulatory agencies.
10. Excellent problem-solving skills and attention to detail.
11. Effective communication skills, both written and verbal.

Personal Attributes:

1. Highly organized and detail-oriented.
2. Proactive and self-motivated, able to work independently and prioritize tasks effectively.
3. Strong team player with the ability to work collaboratively in a fast-paced environment.
4. Adaptable and flexible, able to adjust to changing project requirements and priorities.
5. Committed to safety and environmental stewardship.
6. Passionate about continuous learning and professional development in the field of tailings engineering.

This is a remote position.

Draft and review legal documents, contracts, pleadings, and correspondence

Conduct legal research and case law analysis

Prepare case summaries and assist in trial preparations

Organize and maintain client files and case management systems

Communicate with clients, courts, and third parties professionally and promptly

Provide general administrative support to attorneys and legal teams

Qualifications:

Bachelor's degree in Law, Legal Management, or related field

At least 2 years of experience as a paralegal or legal assistant (U.S. law experience preferred)

Excellent written and verbal English communication skills

Proficient in legal research tools (e.g., LexisNexis, Westlaw) and MS Office/Google Workspace

Detail-oriented, proactive, and able to manage multiple deadlines

Comfortable working remotely and independently

Nice to Have:

Familiarity with U.S. legal systems and court procedures

Experience using legal software (e.g., Clio, MyCase, PracticePanther)

Knowledge in areas such as litigation, corporate law, immigration, or family law

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn .

• Provides input into statistical sections and overall consistency of clinical study protocols.
• Develops and reviews statistical analysis plans (SAP). Determines appropriate analyses for clinical endpoints based on input from the protocol and the client.
• Performs senior-level reviews and is responsible for the datasets and outputs of a project. Ensures consistency with the SAP and reviews for correctness and quality.
• Works with programming team to provide input for analysis/ADaM datasets to be used for final analyses. Develops specifications and reviews datasets based on what is needed for the planned tables, listings and graphs (TLGs).
• Prepares TLG shells/specifications and programming notes based on SAP and analysis/ADaM datasets.
• Works with data management team to review data collection (e.g., CRFs) and helps ensure data quality throughout the clinical trial.
• Performs and/or coordinates the preparation, execution, reporting and documentation of high-quality statistical analysis according to the SAP.
• Provides high level of support to the programmers and medical writers on all statistical matters according to client requirements.
• Prepares and reviews statistical methods and results sections for the clinical study report (CSR) with in-house medical writers.
• Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
• Generates sample size calculations appropriate for the primary endpoint and based on input from the protocol.
• Generates and reviews randomization schedules per the protocol and randomization specifications.
• Works with the project management group to ensure timelines are appropriate given the scope of the project.
• Is familiar with and stays current with the latest industry practices and updated regulatory guidelines.
• Communicates competently and independently with client to coordinate the statistical and programming considerations of the project.
• Demonstrates strong understanding of ICH guidelines, as applicable to statistics.
• Practices good internal and external customer service.

• Master of Science (in statistics or equivalent) with four (4) plus years relevant work experience or PhD (in statistics or equivalent) with two (2) plus years of relevant work experience.
• Strong knowledge of and experience with SAS (SAS Stat, SAS Base, SAS macros, SAS/ODS, SAS/Graph).
• Able to be in a hands-on role by digging into data and using SAS to validate datasets and outputs.
• Excellent mathematical and problem-solving skills.
• Advanced knowledge of the statistical considerations involved in drug development including hands-on experience with clinical trial data.
• Strong knowledge of study designs and statistical analysis methods (e.g., GLMs, non-parametric methods, survival analysis techniques, general imputation methods, common descriptive stats).
• Strong familiarity with a variety of clinical data and databases (including EDC systems).
• Working knowledge of SDTM/ADaM standards (in the absence of ADaM experience, considerable experience working with analysis or derived datasets).
• At least three (3) years of experience in pharmaceutical industry.
• Ability to coordinate the analytical aspects of multiple projects or clinical trials at the same time.
• Proficiency with MS Office applications (e.g., Word, PowerPoint and Excel).
• Good interpersonal, oral, and written communication skills.
• Self-motivated, hardworking, dependable, and positive team-oriented personality.
• Ability to communicate effectively and provide clear directions to Statistical Programmers.

Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn .

• Provides input into statistical sections and overall consistency of clinical study protocols.
• Develops and reviews statistical analysis plans (SAP). Determines appropriate analyses for clinical endpoints based on input from the protocol and the client.
• Performs senior-level reviews and is responsible for the datasets and outputs of a project. Ensures consistency with the SAP and reviews for correctness and quality.
• Works with programming team to provide input for analysis/ADaM datasets to be used for final analyses. Develops specifications and reviews datasets based on what is needed for the planned tables, listings and graphs (TLGs).
• Prepares TLG shells/specifications and programming notes based on SAP and analysis/ADaM datasets.
• Works with data management team to review data collection (e.g., CRFs) and helps ensure data quality throughout the clinical trial.
• Performs and/or coordinates the preparation, execution, reporting and documentation of high-quality statistical analysis according to the SAP.
• Provides high level of support to the programmers and medical writers on all statistical matters according to client requirements.
• Prepares and reviews statistical methods and results sections for the clinical study report (CSR) with in-house medical writers.
• Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
• Generates sample size calculations appropriate for the primary endpoint and based on input from the protocol.
• Generates and reviews randomization schedules per the protocol and randomization specifications.
• Works with the project management group to ensure timelines are appropriate given the scope of the project.
• Is familiar with and stays current with the latest industry practices and updated regulatory guidelines.
• Communicates competently and independently with client to coordinate the statistical and programming considerations of the project.
• Demonstrates strong understanding of ICH guidelines, as applicable to statistics.
• Practices good internal and external customer service.

• Master of Science (in statistics or equivalent) with four (4) plus years relevant work experience or PhD (in statistics or equivalent) with two (2) plus years of relevant work experience.
• Strong knowledge of and experience with SAS (SAS Stat, SAS Base, SAS macros, SAS/ODS, SAS/Graph).
• Able to be in a hands-on role by digging into data and using SAS to validate datasets and outputs.
• Excellent mathematical and problem-solving skills.
• Advanced knowledge of the statistical considerations involved in drug development including hands-on experience with clinical trial data.
• Strong knowledge of study designs and statistical analysis methods (e.g., GLMs, non-parametric methods, survival analysis techniques, general imputation methods, common descriptive stats).
• Strong familiarity with a variety of clinical data and databases (including EDC systems).
• Working knowledge of SDTM/ADaM standards (in the absence of ADaM experience, considerable experience working with analysis or derived datasets).
• At least three (3) years of experience in pharmaceutical industry.
• Ability to coordinate the analytical aspects of multiple projects or clinical trials at the same time.
• Proficiency with MS Office applications (e.g., Word, PowerPoint and Excel).
• Good interpersonal, oral, and written communication skills.
• Self-motivated, hardworking, dependable, and positive team-oriented personality.
• Ability to communicate effectively and provide clear directions to Statistical Programmers.

Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.

Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit or follow MMS on LinkedIn .

• Provides input into statistical sections and overall consistency of clinical study protocols.
• Develops and reviews statistical analysis plans (SAP). Determines appropriate analyses for clinical endpoints based on input from the protocol and the client.
• Performs senior-level reviews and is responsible for the datasets and outputs of a project. Ensures consistency with the SAP and reviews for correctness and quality.
• Works with programming team to provide input for analysis/ADaM datasets to be used for final analyses. Develops specifications and reviews datasets based on what is needed for the planned tables, listings and graphs (TLGs).
• Prepares TLG shells/specifications and programming notes based on SAP and analysis/ADaM datasets.
• Works with data management team to review data collection (e.g., CRFs) and helps ensure data quality throughout the clinical trial.
• Performs and/or coordinates the preparation, execution, reporting and documentation of high-quality statistical analysis according to the SAP.
• Provides high level of support to the programmers and medical writers on all statistical matters according to client requirements.
• Prepares and reviews statistical methods and results sections for the clinical study report (CSR) with in-house medical writers.
• Provides support to Data Safety Monitoring Boards (DSMB) by preparing and presenting output as the unblinded statistician.
• Generates sample size calculations appropriate for the primary endpoint and based on input from the protocol.
• Generates and reviews randomization schedules per the protocol and randomization specifications.
• Works with the project management group to ensure timelines are appropriate given the scope of the project.
• Is familiar with and stays current with the latest industry practices and updated regulatory guidelines.
• Communicates competently and independently with client to coordinate the statistical and programming considerations of the project.
• Demonstrates strong understanding of ICH guidelines, as applicable to statistics.
• Practices good internal and external customer service.

• Master of Science (in statistics or equivalent) with four (4) plus years relevant work experience or PhD (in statistics or equivalent) with two (2) plus years of relevant work experience.
• Strong knowledge of and experience with SAS (SAS Stat, SAS Base, SAS macros, SAS/ODS, SAS/Graph).
• Able to be in a hands-on role by digging into data and using SAS to validate datasets and outputs.
• Excellent mathematical and problem-solving skills.
• Advanced knowledge of the statistical considerations involved in drug development including hands-on experience with clinical trial data.
• Strong knowledge of study designs and statistical analysis methods (e.g., GLMs, non-parametric methods, survival analysis techniques, general imputation methods, common descriptive stats).
• Strong familiarity with a variety of clinical data and databases (including EDC systems).
• Working knowledge of SDTM/ADaM standards (in the absence of ADaM experience, considerable experience working with analysis or derived datasets).
• At least three (3) years of experience in pharmaceutical industry.
• Ability to coordinate the analytical aspects of multiple projects or clinical trials at the same time.
• Proficiency with MS Office applications (e.g., Word, PowerPoint and Excel).
• Good interpersonal, oral, and written communication skills.
• Self-motivated, hardworking, dependable, and positive team-oriented personality.
• Ability to communicate effectively and provide clear directions to Statistical Programmers.

Please consider your application unsuccessful if we do not reach out to you within 14 days of your submission.