91 Safety Standards jobs in South Africa
Quality Control
Roodepoort, Gauteng
R45000 - R180000 Y
IPS: Health and Wellness
Posted today
Job Viewed
Job Description
We're Hiring: Quality Control (QC) Consultant
Location:
Johannesburg (Hybrid options available)
Salary:
R16,500 basic (p/m) + incentives
Closing Date:
08 September 2025
At
IPS Health & Wellness
, we're looking for a detail-driven
Quality Control Consultant
to join our dynamic QC team. This is
not a lab or product QC role
– instead, you'll be at the heart of ensuring our customer interactions are professional, compliant, and aligned with our standards.
What you'll do:
- Listen to and analyse call recordings across Sales, Client Care, Lead Generation, and Retentions.
- Provide constructive feedback to consultants and managers to drive performance.
- Verify and enhance QC notes with insights that capture the consultant's perspective.
- Recommend improvements to scripts, compliance adherence, and overall customer experience.
What we're looking for:
- A
Bachelor's degree (3 years minimum)
. - Strong communication skills in
English and Afrikaans
(other languages are a plus). - Someone who is objective, trustworthy, and discreet.
- Analytical thinker with a sharp eye for detail.
- Comfortable with call monitoring and quality assurance tools.
- Organised, innovative, and able to work independently and in a team.
- Knowledge of call centre operations and compliance requirements.
Why join us?
- Work 08:00 – 16:30 with
flexitime
available after probation (3 months). - Remote work
opportunities based on performance. - A supportive, growing environment where your feedback directly impacts the customer journey.
- Employment equity principles apply – we strongly encourage applications from designated groups and candidates with disabilities.
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0
Quality Control
R150000 - R250000 Y
Two@Goapply
Posted today
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Job Description
We are seeking a Quality Control Lead with expertise in microbiology, environmental monitoring, and biological testing. The role oversees laboratory operations, ensures compliance with regulatory standards, and drives continuous improvement in microbiological quality systems.
Key Responsibilities:
- Lead QC microbiology operations, including sterility testing, microbial identification, and bioburden analysis.
- Oversee environmental monitoring programs for cleanrooms, utilities, and controlled areas.
- Ensure adherence to GMP, GLP, and regulatory requirements (FDA, EMA, WHO, SAHPRA).
- Review and approve test results, protocols, deviations, and CAPAs.
- Train and mentor microbiology analysts, ensuring technical competency and compliance.
- Collaborate with manufacturing, QA, and regulatory teams to support product release and investigations.
- Drive improvements in laboratory practices, data integrity, and contamination control strategies.
Requirements:
- Bachelor's degree or higher in Microbiology, Biotechnology, or related life sciences field.
- 6+ years' experience in pharmaceutical microbiology or biological QC testing, with at least 2 years in a leadership/supervisory role.
- Strong knowledge of GMP regulations, environmental monitoring programs, aseptic techniques, and cleanroom standards.
- Experience with microbial identification systems (e.g., MALDI-TOF, PCR-based methods).
- Proven ability to manage teams, audits, and cross-functional projects.
- Excellent problem-solving and decision-making skills.
Preferred:
- Master's degree in Microbiology or related field.
- Experience with vaccines, biologics, or sterile drug product manufacturing.
- Prior involvement in regulatory inspections.
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1
Quality Control
R900000 - R1200000 Y
Avacare Health Group
Posted today
Job Viewed
Job Description
Job Title: Quality Control (QC) Analyst
Location: Cape Town, Ndabeni
Contract Type: Permanent
About the Role:
Barrs Pharmaceutical Industries (Pty) Ltd is seeking a skilled and experienced Quality Control Analyst to join our Quality team. This role is key in ensuring the highest quality standards for our raw materials, in-process samples, and finished products.
Key Responsibilities:
- Conduct raw material, in-process, stability, and finished product testing.
- Perform analytical and microbiological testing in compliance with SOPs and GMP standards.
- Operate and maintain laboratory equipment including HPLC, density meter, pH meter, potentiometer, Karl Fischer, conductivity meter, and other analytical instruments.
- Prepare, record, and interpret test results accurately and on time.
- Support continuous improvement in QC processes and maintain laboratory documentation.
- Assist in investigations, deviations, and reporting as required.
Qualifications & Experience:
- Tertiary qualification in Chemistry, Biotechnology, Microbiology or a related field.
- 3–4 years' experience as a QC Analyst in the pharmaceutical or manufacturing industry.
- Hands-on experience with raw material testing, analytical chemistry, microbiology, and stability testing.
- Proficiency in operating HPLC and other key analytical equipment.
- Strong knowledge of GMP, GLP, and regulatory compliance.
Key Competencies:
- High attention to detail and accuracy.
- Strong problem-solving and analytical skills.
- Ability to work independently and as part of a team.
- Excellent communication and reporting skills.
How to Apply:
Interested candidates are invited to submit their CV and supporting documents to
Closing date: 19 September 2025
Please note: Only shortlisted candidates will be contacted. Should you not hear from us within 2 weeks after the closing date of applications, please consider your application unsuccessful.
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2
Quality Control Officer
Johannesburg, Gauteng
SAICA
Posted today
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Job Description
Are you determined to go further as a Difference Maker? SAICA has a perfect opportunity to take you further on your journey of being a Difference Maker. SAICA has embarked on an exciting transformation to become an insights-driven, technology-enabled, and AI-powered organisation. As part of our journey, we are streamlining processes, enhancing our digital capabilities, and strengthening our focus on sustainability in the accounting profession. This transformation presents an opportunity for you to grow and contribute to SAICAs vision in a redefined, future-fit role. We are looking for passionate, skilled professionals who are eager to innovate, embrace datadriven decision-making, and help shape the future of the profession. If you are ready to be part of this next chapter, make a meaningful impact, and you are a suitably qualified and experienced Difference Maker wanting to go further on this exciting journey, you are encouraged to apply. Purpose of the job To plan and perform timely internal quality control assessments for member discipline function to ensure compliance and to provide technical assistance in accounting to Member Discipline Team. Key/main outputs Output 1: Quality Control- stats Plan and perform timely internal quality control assessments of statistics and reporting relating to : Complaints received; Complaints finalised through various platforms; On-going complaints and age analysis; Tracking Schedules And report into DDO on a quarterly and annual basis Reviewing of tables, statistics and other data required by the DDO and prepared by the Member Discipline attorneys and paralegals, for reporting to Board; Integrated Reporting; Regulatory reporting and monitoring and internal audit to ensure accuracy and compliance Output 2: Quality Controls for Legal Sharedrive documentation; Disciplinary Case management system; D365 queries and Discipline Page on website. Quality control functions on archived case files and hearings content in required format Regular comparing of Disciplinary Case management system with complaints registers to ensure data integrity and accuracy Tracking of Member Discipline Units D365 query resolution to ensure compliance Tracking of compliance with regulators requirements in terms of referred cases and reporting Quality control assessments for publication matters and matters that require removal from website Quality control of Discipline related documentation on SAICA website/member portal Output 3: Quality control of Disciplinary documentation and Expense tracking To ensure the disciplinary documentation in case files comply with the requirements of the By-laws and Disciplinary Code ; Tracking of expenses relating to hearings ; service providers and external law firms to update the DDO and ensure compliance with allocated budget Output 4: Technical Accounting Advice Provides technical consultations to Member Discipline Team and pro-forma prosecutors where required and assists with review of complex, highly technical complaints /charge sheets; may be required to give evidence at PCC/DC and/or external hearings. Required to perform ad hoc special projects as determined by the DDO Output 5: Embrace and drive organisational transformation Actively contribute to cost containment efforts by identifying opportunities for operational efficiencies, optimising resources, and ensuring value-driven decision-making in daily activities. Support SAICAs transformation into an insights-driven organisation by leveraging data and analytics to enhance decision-making, improve processes, and drive continuous improvement in your area of work. Effectively utilise digital tools and technology to enhance productivity, streamline workflows, and improve service delivery. Stay informed about new and emerging technologies relevant to your role. Adopt and embrace AI-driven tools and automation to enhance efficiency, accuracy, and effectiveness in job-related tasks, while continuously seeking opportunities to improve processes through innovative technology solutions. Identify and support SAICAs management of risks related to sustainability, including environmental risks, regulatory changes and social risks and integrating them into business continuity and risk management plans. Formal Education Accounting qualification is required. Technical/ Legal Certification Certification/membership of Institute of Internal Auditors, SA would be advantageous; completion of trainee accountant articles would be advantageous Experience 5 years' experience in internal audit environment and experience in providing technical accounting advice; advanced skills in excel Knowledge and Skills Business Acumen: Knowledge and understanding of the principles of business, the application thereof, the opportunities within business and the seizure of such opportunities Financial Knowledge: Knowledge and understanding of financial practices and standards prescribed by regulation authorities Information Technology: Understanding of ICT prescribed practices and legislative requirements for data security and information management Governance and Compliance: Ability to implement and follow governance and compliance procedures Detail Focused: The ability to attend to finite detail whilst executing outputs to ensure the quality-of-service delivery Administrative: The ability to use knowledge of administrative techniques, tools policies and/or procedures to provide enabling functions Analytical: The ability to analyse situations and to arrive at the best possible solution Problem Solving: The ability to apply the principles of problem-solving techniques to identify and resolve a problem in the best interest of all stakeholders Critical Thinking: The ability to conduct disciplined intellectual criticism that combines research, knowledge of historical context, and balanced judgment Organising: To apply or impose efficient working methods in order to work effectively or make somebody else work effectively Communication: The ability to communicate effectively and efficiently at all levels in the organisation
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3
Quality Control Superintendent
Saldanha, Western Cape
Sea Harvest Group Ltd
Posted today
Job Viewed
Job Description
Overview
Join to apply for the Quality Control Superintendent role at Sea Harvest Group Ltd .
Responsibilities- To ensure that initiating,implementation and maintenance of all aspects of Food Safety and Quality Control as outlined in the Companies Foodsafety/Quality Management Systems pertaining to frozen incoming materials is adhered to
- Entry level
- Full-time
- Management and Manufacturing
- Fisheries
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4
Quality Control Manager
Centurion, Gauteng
Virbac Group
Posted 2 days ago
Job Viewed
Job Description
Supervise and carry out all laboratory activities involved with the analyses of materials and products to cGLP/cGMP standards. Maintain QC infrastructure to ensure timeous and accurate analytical results for all products to meet customer and cGxP requirements.• Managing a team of laboratory staff and developing operating procedures to ensure that experiments and analyses are conducted within budgets and according to established scientific standards • Prioritizing and allocating laboratory operations and workflow so that the laboratory’s equipment and resources are used efficiently and work schedules and targets are met • Researching, evaluating, and recommending investments in technology, equipment, systems, or other assets that will enhance the laboratory’s performance**Management of People*** Propose resource requirements and appropriate organisational structure to meet strategic missions, critical success factors and business outcomes for the department. Manage and support the recruitment of staff with the right experience, competencies that fit with the Virbac culture.* Provide ongoing feedback and coaching to direct reports in order to ensure they meet the expectations of performance, and to develop and support them in their role.**Quality Control*** Allocate work to the focus stations in the Quality Control Laboratory. Optimise testing costs and throughput times according to continuous improvement objectives.* Check and sign-off all laboratory results of testing conducted by Laboratory Analysts including a check to ensure the correct method was used and reviewing of raw data.* Ensure that all errors, overwriting and blank spaces on worksheets are deleted and signed for per SOP (14)9 Good Documentation Practice.* Ensure that all HPLC printouts are initialled and dated by the Lab Analyst and the reviewer.* Ensure that the necessary QC documentation is maintained in line with current Good Laboratory Practice (cGLP).* Ensure that information is completed on the Trending spreadsheet for API, FP and RO water* Ensure analyses are conducted timeously according to prescribed methods and plan, with priority given to backorder and essential products.* Ensure that the weekly Laboratory Schedule is updated twice a week.* Communicate any delays in testing to the relevant stakeholders within 1 day of identifying the delay.* Ensure that products are tested within their agreed timelines as per the Laboratory Schedule.* Ensure analytical methods are validated as per the required schedule.* Ensure analytical method transfers are planned and completed as per the required schedule* Ensure laboratory productivity and efficiency to meet business requirements.* Compile, maintain and update the Products in Q sheet.* Ensure that reagents, reference standards and other consumables are ordered at least 1 month before expiration or consumption to avoid delays in release.* Ensure that POs and Tax Invoices are submitted for payment* Maintain high standards of cGLP at all times.* Conduct method development as required.* Ensure out of specification reports are initiated immediately when an OOS is identified and investigated.* All OOSs must be immediately communicated to the relevant stakeholders.* Ensure that there is an annual inhouse Lab Plan in place for the following year by the end of Q3 of each current year.* Perform analysis where an analyst is not available or as dictated by the workload.* Any other requests as deemed reasonable by your Manager**Documentation Management*** Ensure that analytical methods are current and aligned to the dossier.* Ensure that the filing system is in place to ensure safe storage and easy retrieval of documents related to analytical processes.* Ensure that Laboratory Analysts compile all Laboratory Reports as the prescribed SOP.* Ensure that Laboratory Analysts file all Laboratory Reports and raw data after completion of each analysis.* Ensure both computer generated and hard copy documentation are filed accurately according to cGLP and Good Documentation requirements* Ensure that all computer generated documents are backed up and easily retrievable.* Ensure that all Laboratory Reports and raw data are archived annually.* Draw up certificates of analysis (lab reports) as required.**Compliance*** Ensures cGLP, Health & Safety and housekeeping codes are enforced according to appropriate procedures.* Ensure that Standard Operating Procedures are in place and up to date and adhered to for all critical activities as prescribed by the guidelines.* Ensure no critical findings during external audits by external parties.* Ensure closure of 90% of current self-inspection audit findings within a 12 month period.* Participate in investigations relating to product quality complaints, OOS, Root Cause Analysis and similar which affect the QA department.* Ensure staff are trained on cGLP and SOPs as required.* Compile, review and update of SOPs related to your function. Ensure that these SOPs are updated within the review date.* Complete training of personnel for SOPs where you are the initiator/ trainer.* Ensure that all corrective and preventative actions, deviations and change controls are closed within the agreed timeline.* Download and review of the temperature monitoring data for the laboratory and reference standard fridge on a weekly basis.* Report any temperature excursions to the Quality Manager immediately.* Submission of the temperature monitoring data to the Quality Manager on a monthly basis for review and approval.**Asset Management and Housekeeping*** Adhere to the NIP process when procuring new equipment, instruments or NIP related items.* Ensure equipment is maintained and calibrated and qualified as per predetermined plan and is in good working order.* Motivate for new/replacement equipment and infrastructure.* Deploy equipment and related resources to maximize output.* Ensure that Laboratory equipment efficiency targets are met.* Ensure that housekeeping is completed as per the prescribed SOP.* Ensure that safety standards are maintained.* Ensure adherence to calibration and preventative maintenance schedule.* Ensure laboratory waste is disposed of in an environmentally responsible manner.**Reporting*** Preparation of a monthly report on the laboratory's activities including but not limited to output, capacity, compliance, human resource and specific projects in progress within the department.* Submission of report to Quality Manager 1 working day before the meeting.**Budget Management*** Operate within approved OPEX/CAPEX budgets.* Review departmental expenses monthly and plan accordingly to ensure compliance to set budget.**Requirements*** National Diploma in Analytical Chemistry* BSc Chemistry or B Tech Chemistry equivalent qualification (NQF 7) – preferred* Supervisory/ team leader experience* 5 years Pharmaceutical Laboratory experience with team leadership and cGxP compliance experience (minimum 5+ years Pharmaceutical laboratory experience with at least 2 years supervisory and cGxP compliance experienceVirbac provides numerous career opportunities, thanks to the diversity of its jobs and their international dimension.Joining Virbac means joining dynamic teams ambitious for success.Add Your Talent to Ours!**Experiencing together a unique human adventure**Animal health is key to the health of the planet. Working at Virbac means taking part in a unique human adventure in which the engagement of each individual contributes to its evolution. Encouraging internal mobility between positions and countries, offering individual development plans and building a partnership based on trust between managers and employees are as many perspectives of motivation for our teams. We also offer them a work environment conducive to exploring new territories and balancing their professional and personal lives. Finally, fostering their engagement to animal
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5
Quality Control Inspector
Cape Town, Western Cape
ExecutivePlacements.com - The JOB Portal
Posted 3 days ago
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Job Description
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3 days ago Be among the first 25 applicants
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Recruiter:
West Coast Personnel
Job Ref:
JAAD -1
Date posted:
Tuesday, June 3, 2025
Location:
killarney gardens, Western Cape, South Africa
Salary:
R10,000 per month
SUMMARY:
Quality Control Inspector
POSITION INFO:
Job Summary:
The Quality Control Inspector in the Plastic Injection Moulding Department is responsible for inspecting products, materials, and processes to ensure they meet quality standards and comply with industry specifications. This role includes assessing the quality of incoming materials/products, in-process products, and finished items, ensuring that defective products are identified and corrective actions are recommended.
Responsibilities:
Product Inspection:
- Perform regular quality checks on raw materials, in-process products, and finished goods to verify they meet established quality standards.
- Monitor and document injection moulding processes to ensure consistency and compliance with specifications.
- Identify defects or deviations from specifications, document findings, and report to the Quality Control Team Leader.
- Maintain accurate and detailed inspection records, including product samples and any non-conformance findings.
- Conduct and document standard tests, such as dimensional checks, visual inspections, and functional tests, using precision measuring equipment (e.g., gauges).
- Provide feedback on potential areas for improvement to production teams and support corrective action implementation.
- Work closely with production and engineering teams to address quality issues and implement solutions.
- Assist in training production staff on quality standards and inspection procedures as required.
- Ensure compliance with safety and health regulations during inspections and handling of materials.
Requirements:
- Matric certificate or equivalent
- Minimum 1 year of experience in quality inspection or manufacturing (injection moulding preferred)
- Familiarity with injection moulding processes and common plastic defects (e.g., flash, sink, warping)
- Ability to read and interpret technical drawings, part specifications, and inspection standards
- 1 year experience in the use of precision measuring tools, e.g.
- Vernier callipers
- Micrometres
- Height gauges
- Go/no-go gauges
- Basic understanding of quality standards (e.g., ISO 9001) and inspection procedures
- Strong attention to detail and ability to spot visual and dimensional defects*
- Physical Requirements:
- Ability to stand for long periods
- Lift parts or tools
- Comfortable working in production floor environment (hot, noisy, etc.)
- Basic computer skills for data entry and reporting*
- Good communication skills to report findings and work with production staff
- Seniority level Entry level
- Employment type Full-time
- Job function Quality Assurance
- Industries Advertising Services
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6
Quality control operator
Johannesburg, Gauteng
Buffalo
Posted 3 days ago
Job Viewed
Job Description
Summary:
Perform quality control checks on products before processing to ensure compliance with company standards and supplier requirements. Conduct inspections on all item being processed and address defects, deviations, or non-conformities.
Key Responsibilities:
- Inspect products, materials before processing stage.
- Ensuring daily demand targets of parcels being processed are met.
- Identify and isolate non-conforming products or materials. Notify production staff and manager of quality issues.
- Collaborate with production teams to resolve quality problems.
- Maintain a clean and organized work environment.
Requirements:
- High school matric.
- 1-2 years of warehousing operations experience and knowledge of quality control principles.
- Analytical and problem-solving skills. Attention to detail and accuracy is crucial.
- Effective communication and teamwork skills. Ability to work in a fast-paced environment.
- Basic computer skills (e.g., data entry, reporting).
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7
Quality Control Supervisor
Johannesburg, Gauteng
ExecutivePlacements.com - The JOB Portal
Posted 3 days ago
Job Viewed
Job Description
Join to apply for the Quality Control Supervisor role at ExecutivePlacements.com - The JOB Portal
3 days ago Be among the first 25 applicants
SUMMARY: Our client based in Johannesburg specializes in packaging for the food and beverage, pharmaceutical, household, and personal care markets.
Recruiter: Stratogo
Job Ref: HQ /pn
Date posted: Saturday, November 23, 2024
Location: Johannesburg, South Africa
Salary: Monthly
Position Info:
- Purpose of the Role: To ensure products manufactured conform to quality, safety, and reliability standards
- Role: Quality Control Supervisor
- Industry: Manufacturing - Packaging
- Qualifications: Matric, NQF 4 - Supervisory Management Qualification, Certificate in Quality Control
- Skills: People management skills, Attention to detail, Problem solving skills
- Competencies: Technical knowledge of process, inclusive of equipment and raw materials; Relevant quality system and certification; Diversity Management; Conflict Management
Quality Control Planning:
- Develop and implement quality control procedures and protocols to ensure compliance with company standards and regulatory requirements.
- Conduct regular audits
- Develop and maintain quality control records, including documentation of test results, inspection reports, and corrective actions taken.
Personnel Management: Responsible to lead, motivate and train subordinates
Customer Service: Responsible for customer inquiries regarding product quality and providing resolutions to customer complaints.
Reporting and Administration
Health and Safety
Food Safety Systems Certification - FSSC
Self Development and Growth
Seniority level- Mid-Senior level
- Full-time
- Quality Assurance
- Manufacturing - Packaging
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8
Quality Control Supervisor
Gauteng, Gauteng
Kemin Industries
Posted 4 days ago
Job Viewed
Job Description
Overview
Join to apply for the Quality Control Supervisor role at Kemin Industries .
The QC Supervisor is responsible for organizing daily activities, maintenance and troubleshooting of lab instruments, and communicating day-to-day QC affairs between departments.
Responsibilities- Guide day-to-day QC activities.
- Release raw materials and finished goods as authorized, as applicable.
- Coach and train team.
- Report major batch record variances, as applicable.
- Follow and contribute to procedures and SOPs/forms.
- Maintain proper quality documentation.
- Generate and review Certificates of Analysis.
- Support Change Management functions.
- Ensure good laboratory practices and safety protocols are followed; apply 5S+1.
- Participate in internal audits, as applicable.
- Provide support with external audits, as applicable.
- May collect samples, prepare shipments, and inspect raw materials and finished goods.
- Perform various types of raw material testing.
- Enter data daily and run reports in ERP systems, as defined and applicable.
- Perform lot tracing as applicable.
- Report nonconformities by following applicable SOPs; generate nonconformity reports and communicate to stakeholders, as applicable.
- Coordinate with QA to determine a rework plan.
- Review supplier qualification tests, as applicable.
- Investigate Corrective Action/Preventive Action (CAPA) as assigned.
- Write and approve method validation protocols.
- Contribute to reports and deliver internal presentations.
- Lead QC projects and participate in PIP meetings; inform management of updates.
- Participate in and/or lead product scale-up activities.
- Identify opportunities for process innovation.
- Collaborate with cross-functional teams (including Operations, R&D, quality groups) and other departments.
- May provide input to budget, as applicable.
- Foster an environment of food and/or feed safety in compliance with applicable rules and regulations.
- Bachelor’s Degree (4-year) in a related field with 5+ years of related experience.
- Master’s Degree with 2+ years of related experience.
- Advanced working knowledge of lab instruments, as applicable.
- Strong written and oral communication skills.
- Proficiency with computer systems, including MS Office, M3 and LIMS, etc.
- Attention to detail.
- Project management skills.
- Familiarity with SPC principles and practices.
- Ability to operate, troubleshoot, perform maintenance, instruct, and perform method validation on lab equipment.
- Ability to interact well with others in a team environment.
- Lifelong learning mindset.
- Mid-Senior level
- Full-time
- Quality Assurance and Training
- Biotechnology Research and Animal Feed Manufacturing
Location: Clayville, Gauteng, South Africa
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