What Web Application Testing Jobs are in South Africa?
Showing 142 Web Application Testing jobs in South Africa
Senior Full Stack Developer - Web Applications
1939 Vereeniging
Placements24
Posted 9 days ago
Job Viewed
Job Description
About the Role
Our client, a dynamic marketing technology company, is seeking a talented Senior Full Stack Developer to join their team in Vereeniging, Gauteng . This role is integral to developing and enhancing their cutting-edge web applications, delivering sophisticated solutions to their diverse clientele. You will be involved in both front-end and back-end development, working with modern frameworks and technologies to build user-friendly and high-performing applications. The ideal candidate will have a strong foundation in web development principles, a passion for creating exceptional user experiences, and a proven ability to contribute effectively in a collaborative team environment. This is an on-site position, offering the chance to work closely with colleagues in a stimulating office setting located in Vereeniging . We are looking for a driven individual who can take ownership of projects, contribute to architectural decisions, and mentor junior developers. Your expertise will be crucial in driving innovation and ensuring the technical excellence of our client's product suite.
Key Responsibilities- Develop and maintain robust, scalable web applications using modern full-stack technologies (e.g., React, Angular, Vue.js for frontend; Node.js, Python, Java, or .NET for backend).
- Design and implement efficient database schemas and queries (SQL and/or NoSQL).
- Build and integrate RESTful APIs for seamless data exchange.
- Write clean, efficient, and well-documented code across the entire stack.
- Collaborate with UI/UX designers, product managers, and other developers to translate requirements into functional features.
- Optimize application performance for speed and scalability.
- Implement comprehensive unit and integration tests to ensure code quality.
- Participate in code reviews and provide constructive feedback to peers.
- Troubleshoot, debug, and resolve issues across the full application stack.
- Stay up-to-date with emerging web development trends and technologies.
- Bachelor's degree in Computer Science, Software Engineering, or a related field, or equivalent work experience.
- 5+ years of professional experience in full-stack web development.
- Proficiency in frontend technologies such as HTML, CSS, JavaScript, and modern frameworks (React, Angular, Vue.js).
- Strong experience with backend development languages and frameworks (e.g., Node.js/Express, Python/Django/Flask, Java/Spring, C#/.NET).
- Experience with relational databases (e.g., PostgreSQL, MySQL) and/or NoSQL databases (e.g., MongoDB).
- Familiarity with cloud platforms (AWS, Azure, GCP) and deployment practices.
- Understanding of CI/CD principles and tools.
- Excellent problem-solving, analytical, and debugging skills.
- Strong communication and interpersonal skills.
- Ability to work effectively in a team-oriented environment.
- Competitive annual salary.
- On-site work environment in Vereeniging .
- Comprehensive health insurance package.
- Pension fund contribution.
- Generous annual leave.
- Opportunities for professional development and training.
- Collaborative and innovative work culture.
- Potential for performance-based bonuses.
- Modern office facilities.
- Regular team-building events.
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Job Description
The role focuses on verification testing across firmware and hardware modifications for embedded IoT devices, ensuring product reliability, functionality and compliance with quality standards.
You will execute structured test cycles covering startup sequences, operating systems, menu functionality, command execution, calibration verification, device integrations and communication performance. The role also supports production, tooling, manufacturing diagnostics, and test fixture activities within a technically driven environment.
Minimum Requirements
- Diploma or Certificate in Electronics, Electrical Engineering, or related technical field.
- Minimum 3 years hands-on electronics testing experience.
- Proven experience testing embedded electronic devices or IoT products.
- Experience using electronic test equipment and measurement tools.
- Ability to interpret schematics and component datasheets.
- Strong troubleshooting ability, attention to detail, structured testing methodology, and excellent problem-solving skills are essential.
Advantageous Experience
- Telematics or automotive electronics testing.
- Vehicle integration testing.
- Embedded communication systems testing.
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1
Job Description
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Job Description
If you meet the above requirements, please send the following to
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Job Description
Minimum Requirement
- Grade 12
- N6 Certificate or National Technical Diploma
- Electrical Trade Test Certificate
- Minimum of 2 to 3 years experience as a Trade Tested Electrician in a manufacturing Industry
- Strong knowledge of electrical systems, components and tools
- Familiarity with electrical codes, regulations and safety standards
- Excellent trouble shooting and problem solving skills
- Good communication and interpersonal skills
- Able to work independently
- Willingness to work shift, including evenings, weekends and overtime as needed
- Clear criminal record
- Traceable reference
Duties and Responsibilities
- Preventative and Reactive Maintenance, executing scheduled maintenance plans
- Performing routine inspections, and rapidly troubleshooting electrical breakdowns to minimize downtime
- Tracing and repairing electrical faults on single phase and three -phase systems, low voltage equipment and control panels
- Regularly inspect electrical systems, circuits and equipment to identify potential hazards or malfunctions
- Report any electrical problems, safety concerns or potential risks to the Maintenance Manager or relevant personnel
- Adhere to all safety protocols, procedures and regulations to ensure a safe working envirnment
- Ensure empliance with local , state and federal electrical codes and regulations
- Respond promptly to electrical emergencies or breakdowns to minimize downtime and ensure the safety of personnel and equopment
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4
Job Description
Minimum requirements for the role:
- Must have a Master's Degree (MSc) in Agronomy, Crop Science, Soil Science, Plant Physiology, or a related agricultural discipline; A PhD in a relevant agricultural field would be highly advantageous
- Proven experience managing agricultural field trials and research programmes
- Must have a strong understanding of experimental design, scientific methodology, and statistical analysis
- Extensive knowledge of plant physiology, soil health, crop nutrition, and crop production systems
- Experience working across multiple crop categories including horticultural, row, and specialty crops would be advantageous
- Strong analytical and data interpretation capabilities
- Experience managing small teams and coordinating field operations
- Excellent report writing and scientific communication skills
- Strong computer literacy, including experience with data analysis and reporting software
- Must have a valid driver's license and own reliable vehicle with willingness to travel extensively throughout the trial territory
- Fluency in both Afrikaans and English (Read, Write, Speak)
- Must be based in Limpopo or willing to relocate to the region
The successful candidate will be responsible for:
- Designing, implementing, and managing agricultural field trials across approximately 20 farms within the Limpopo region.
- Ensuring trial protocols are followed accurately, maintaining scientific integrity and consistency across all locations.
- Managing treated versus untreated comparison plots and ensuring reliable, repeatable, and statistically meaningful trial outcomes.
- Conducting regular field inspections and monitoring crop development throughout the growing season.
- Ensuring all trial activities align with approved research methodologies and scientific best practices.
- Coordinating trial scheduling, sampling activities, and seasonal evaluations.
- Collecting, analysing, and interpreting agronomic data across multiple crop types.
- Conducting and overseeing soil sampling, soil health assessments, tissue analysis programmes, plant physiological measurements, crop growth monitoring, yield assessments, and quality evaluations.
- Monitoring key plant performance indicators including chlorophyll content, fruit and berry sizing, flower counts and fruit set ratios, internode development, canopy temperature, soil compaction measurements, and root and plant health indicators.
- Ensuring accurate data capture, record keeping, and reporting standards.
- Maintaining databases and trial records to support analysis and decision-making.
- Building and maintaining strong working relationships with participating farmers and agricultural stakeholders.
- Conducting regular farm visits and providing practical agronomic support where appropriate.
- Ensuring farmers understand trial objectives, protocols, and data requirements.
- Acting as the primary local point of contact between South African trial sites and the US-based leadership team.
- Representing the company professionally at all times while promoting a scientific and data-driven approach.
- Recruiting, training, mentoring, and managing field assistants involved in trial execution.
- Ensuring consistency and quality of field assessments through coaching and supervision.
- Monitoring team performance and ensuring all field activities are completed safely and accurately.
- Promoting a culture of professionalism, accountability, and scientific excellence.
- Preparing weekly, interim, and final trial reports for management and stakeholders.
- Presenting findings, recommendations, and observations in a clear and professional manner.
- Participating in regular virtual meetings with US-based leadership teams.
- Maintaining a high level of responsiveness to communication and reporting requirements.
- Ensuring deadlines are consistently met and reporting standards are maintained.
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5
Job Description
Minimum requirements for the role:
- Must have a tertiary Agricultural qualification such as a B. Sc. Degree in Plant Production/Plant Science/Plant Pathology or similar field of study
- Sound knowledge of irrigation, crop protection, and plant nutrition practices
- Computer literate with proficiency in Microsoft Office applications
- Willingness to work flexible hours
- Must have a valid driver's license with willingness to travel extensively throughout South Africa, including early mornings, late afternoons, evenings, and overnight stays when operationally required
The successful candidate will be responsible for:
- Planning seasonal trials.
- Planning trial layouts.
- Implementing trials.
- Evaluating trials.
- Capturing trial data and reporting trial results.
- Packing trial seed.
- Managing crops.
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6
Principal Regulatory Affairs Specialist (Global Clinical Trial Applications)
Remote
ThermoFisher Scientific
Posted 9 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We are currently seeking a **Principal Regulatory Affairs Specialist** to join our global Regulatory Affairs department, Reg Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.
In this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials, studies and projects.
You will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance.
You will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients.
You will act as a representative of the regulatory department with other departments, supporting business development, working on initiatives, and contributing to quality improvement. You will also arrange, lead, and report on client and regulatory agency meetings.
**The following skills are required to be successful in this position:**
+ preparation and assembly of global regulatory submissions (CTA)
+ interacting with sponsors,
+ review and assess clinical trial regulatory documents,
+ review and assess scientific literature.
+ manages project teams and preparation
+ participate in launch meetings, review meetings and project team meetings.
+ Experience with bid defense meetings
**Qualifications**
What the role requires you to have:
+ Bachelor's degree or advanced degree preferred, or equivalent and relevant formal academic / vocational qualification
+ Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 8+ years
+ Knowledge of the global clinical trials landscape
**Knowledge, Skills and Abilities:**
+ Excellent command of the English language (written and oral) as well as local language where applicable
+ **Experience with Bid Defense meetings**
+ **Experience in leading global regulatory projects for Clinical Trial Applications**
+ Excellent attention to detail and quality as well as excellent editorial/proofreading skills
+ Exceptional interpersonal skills to work effectively in a team environment and act as a liaison with other departments
+ Advanced computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies
+ Strong organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects
+ Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables
+ Excellent understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization; expert knowledge of ICH and other global regulatory guidelines
+ Excellent analytical, investigative and problem-solving skills
**What we offer:**
At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - **_Integrity, Intensity, Innovation and Involvement_** - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies.
With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.
We are currently seeking a **Principal Regulatory Affairs Specialist** to join our global Regulatory Affairs department, Reg Science team. This is a fantastic opportunity to further develop your regulatory career and expertise in a global clinical trial setting.
In this role you will be a pivotal team member with regulatory affairs responsibilities, leading discussions, and coordinating regulatory strategies globally on assigned (Phase 1 to 4) clinical trials, studies and projects.
You will be part of a global team providing innovative solutions and global regulatory expertise, being client interfacing to provide strategic regulatory intelligence and guidance.
You will feel confident providing regulatory advice and carry out projects in the provision of regulatory affairs services whilst acting as liaison with internal and external clients.
You will act as a representative of the regulatory department with other departments, supporting business development, working on initiatives, and contributing to quality improvement. You will also arrange, lead, and report on client and regulatory agency meetings.
**The following skills are required to be successful in this position:**
+ preparation and assembly of global regulatory submissions (CTA)
+ interacting with sponsors,
+ review and assess clinical trial regulatory documents,
+ review and assess scientific literature.
+ manages project teams and preparation
+ participate in launch meetings, review meetings and project team meetings.
+ Experience with bid defense meetings
**Qualifications**
What the role requires you to have:
+ Bachelor's degree or advanced degree preferred, or equivalent and relevant formal academic / vocational qualification
+ Previous experience that provides the knowledge, skills, and abilities to perform the job comparable to 8+ years
+ Knowledge of the global clinical trials landscape
**Knowledge, Skills and Abilities:**
+ Excellent command of the English language (written and oral) as well as local language where applicable
+ **Experience with Bid Defense meetings**
+ **Experience in leading global regulatory projects for Clinical Trial Applications**
+ Excellent attention to detail and quality as well as excellent editorial/proofreading skills
+ Exceptional interpersonal skills to work effectively in a team environment and act as a liaison with other departments
+ Advanced computer skills including the use of Microsoft Word, Excel, Power Point; capable of learning new technologies
+ Strong organizational, time management, and planning skills to create and follow timelines, conduct long-range planning, adapt to changing priorities and handle multiple projects
+ Capable of working independently and exercising independent judgment to assess sponsor regulatory needs and work with project team members to producing compliant deliverables
+ Excellent understanding of global/regional/national country requirements/regulatory affairs procedures for clinical trial authorization; expert knowledge of ICH and other global regulatory guidelines
+ Excellent analytical, investigative and problem-solving skills
**What we offer:**
At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential.
As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We've grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.
Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - **_Integrity, Intensity, Innovation and Involvement_** - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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7
Job Description
RedCat Recruitment is urgently seeking a suitably qualified and experienced CLAIMS ASSESSOR (TRADE TESTED TECHNICIAN) for a well-established concern, based in Uitenhage, Eastern Cape.
JOB DESCRIPTION / REQUIREMENTS
Grade 12.
Competent computer skills (MS Office, Email / Internet).
Motor Mechanic Trade / Diagnostic Technician Certificate/ Master Technician.
Previous working experience in a similar position is essential in a vehicle dealership environment.
Salary offered : To be discussed
PLEASE ONLY APPLY IF YOU HAVE THE RELEVANT EXPERIENCE / ONLY SUITABLE CANDIDATES WILL BE CONTACTED.
IMPORTANT
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8
Maintenance Technician (Trade-Tested Millwright)
Cape Town
The Recruiters
Posted 6 days ago
Job Viewed
Job Description
Our client, a leading company in the frozen fruit and vegetable processing industry , is seeking a skilled and motivated Maintenance Technician (Trade-Tested Millwright) to join their maintenance team.
This is an excellent opportunity for a hands-on maintenance professional with experience in an FMCG, food processing or packaging environment. The successful candidate will be responsible for maintaining, repairing and optimising production, packaging, refrigeration and plant utility equipment to ensure maximum reliability, efficiency and uptime.
Key Responsibilities
- Maintain, repair and optimise production, packaging, refrigeration and plant utility equipment.
- Execute preventative maintenance schedules to minimise downtime.
- Respond promptly to equipment breakdowns and carry out structured fault-finding.
- Support uninterrupted production through safe, efficient and compliant maintenance practices.
- Maintain utilities and plant infrastructure.
- Assist with maintenance systems, asset management and stores control.
- Identify and implement continuous improvement opportunities.
- Ensure compliance with health, safety, food safety and quality standards.
Minimum Requirements
- Trade-Tested Millwright qualification.
- 35 years'' maintenance experience in an FMCG, food processing or packaging environment .
- Experience working with automated production equipment.
- Strong mechanical and electrical fault-finding skills.
- Experience with:
- 3-phase motors
- Variable Speed Drives (VSDs)
- Pneumatic systems
- Industrial sensors
- Ability to read and interpret wiring diagrams and machine schematics.
- Willing and able to work rotational shifts and weekends.
- Self-motivated with excellent analytical and problem-solving skills.
- Strong verbal and written communication skills.
Key Performance Areas
- Production equipment reliability.
- Preventative maintenance execution.
- Utilities and infrastructure support.
- Maintenance systems and stores control.
- Health, safety and food safety compliance.
Success Measures
- Overall Equipment Effectiveness (OEE).
- Timely response and resolution of equipment breakdowns.
- Preventative maintenance schedule adherence.
- Maintenance costs managed within budget.
- High levels of equipment reliability and plant availability.
To apply, please email your updated CV in Word format together with your ID, driver''s license, qualifications, reference letters or contactable referees, and a recent profile picture of yourself to:
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9