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Results for laboratory in "laboratory" in Jobs in Gauteng in Gauteng
1
Division: Wits Mycology Main purpose of the job:To lead and coordinate the laboratory and scientific components of Wits Mycology research, including the CombAT Candida clinical trial and associated laboratory projectsThe incumbent will support the transition, establishment and ongoing management of the Biohub laboratory facility, ensuring appropriate laboratory systems, workflows and governance are implementedFor CombAT Candida, the incumbent will oversee laboratory workflows for Candida surveillance and clinical trial specimens, ensure high quality processing and stoage of samples, and provide strategic scientific input into study design, analysis and disseminationThe role combines hands-on laboratory work with project management, staff supervision, and coordination between laboratory, clinical and research teamsLocation:1 Modderfontein Road, Sandringham, JohannesburgMore Info:Wits Mycology aims to improve the outcomes of people with varied lived experiences who are affected by life-threatening or disabling fungal diseases through clinical trials, observational studies, social science studies, and laboratory research and innovationOur research also stretches to other important infectious diseases We work in South Africa, across the African continent and globallyKey performance areas: Culture, identification and characterisation of Candida species from clinical and surveillance specimensProcessing, aliquoting and storage of clinical samples including colonisation swabs, blood culture isolates and other specimensMolecular testing including nucleic acid extraction and PCR assaysParticipation in research lab
https://www.executiveplacements.com/Jobs/S/Senior-Medical-Scientist-12-Months-Contract-Wits-H-1274772-Job-Search-03-24-2026-04-34-42-AM.asp?sid=gumtree
9d
Executive Placements
1
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Responsibilities:Weigh and compound of liquid and powder formulations as given by flavourist (Tasting of compounded formulation against retention sample.Application of compounded flavour on applicable base product for testing.Ensure laboratory raw materials are always fresh.Ensure laboratory raw material bottles are filled with factory raw materials.Maintain traceability of raw materials from factory to laboratory.Assist with applicating, packing and labelling of customer samples.File retention samples and formulations of compounded flavours.Maintain sample retention drawer.Compound small in-house stock quantities for production purposes (Compound fresh QC retention sample when requested.Assist with tasting of products for R&D and QC.Responsible for hygiene and general housekeeping of workspace.Requirements:No dietary or religious restrictionsMust be able to tasteBasic knowledge of Food Safety Principles2 yrs exp in the flavour or food industryOnly shortlisted candidates will be contacted.
https://www.jobplacements.com/Jobs/C/Compounder-Flavours-1276169-Job-Search-03-27-2026-10-36-18-AM.asp?sid=gumtree
5d
Job Placements
1
TECHNOLOGIST BACTERIAL LABORATORY ?? Roodeplaat, Pretoria ?? Start Date: 1 May 2026 (earlier start advantageous) ?? Permanent | Post Level 10 (Peromnes)Salary: R480 960 CTC per annum during probation R534 400 CTC upon successful completion of probationMinimum RequirementsSAQA recognised tertiary qualification in Plant Pathology (preferred), Microbiology, Biochemistry or related fieldExperience working in an ISO/IEC 17025:2017 accredited laboratoryExperience with PCR diagnostics, ELISA and microbiological testingPractical laboratory analysis experienceOwnvehicle essentialKey ResponsibilitiesDetection of bacterial pathogens in cropsConduct PCR, ELISA and microbiological assaysEnsure compliance with ISO/IEC 17025 quality systemsSupervise laboratory assistants and support staffMaintain laboratory equipment and testing recordsParticipate in proficiency and inter-laboratory testingAuthorise and interpret laboratory test results
https://www.jobplacements.com/Jobs/T/TECHNOLOGIST--BACTERIAL-LABORATORY-OWN-VEHICLE-ES-1272136-Job-Search-3-16-2026-9-26-23-AM.asp?sid=gumtree
17d
Job Placements
1
Main purpose of the job:To perform on-site laboratory processes and ensure efficient workflow of the onsite laboratoryLocation:7 Esselen Street, Hillbrow, Wits RHI Research Centre Clinical Research Site (CRS)Key performance areas:Co-ordinate all daily lab activities to ensure work is completed within turnaround timeShip samples to outsourced laboratoriesFollow up on DCF and final reports within TATCommunicate laboratory results to doctors/nurses/site coordinators effectively and timeouslyProvide technical input on laboratory results (within scope of practice)Perform laboratory equipment maintenanceLab decontamination and temperature surveillance in the onsite laboratoryPerform backup duties at other Wits RHI on-site labs when requested to do soPerform troubleshooting activities as and when required and ensure communication to the Lab ManagerPerform duties per study Delegation of Authority LogsEnsure equipment maintenance is performed as per maintenance schedules and SOPsMonitor and control stock levels and ensure sufficient stock is available such that lab activities are not adversely affectedTimeous and logical filing of all laboratory recordsDemonstrate cost consciousness and assists in meeting budgetary targetsRepresent the on-site laboratory in meetings as required by managementCommunicate with study team, suppliers, Lab Manager or other stakeholders in a professional and effective mannerComply with Good Clinical Practice (GCP) and standard operating procedures (SOPâ??s) in all lab duties, processes/ activitiesVerify accuracy of data source documentation and accuracy of transcription from source data to Case Reports Forms (CRF) as neededEnsure errors on source documents e.g. CRFâ??s are corrected, initialled and datedSupport the timely transmission/ data faxing or relevant Case Report Forms following QC activity (as needed)Ensure completion of corrective action of internal and external QC reports and monitoring reviewsPerform quality control procedures as Lab SOPS and LQMPEffectively communicate/ report all quality challenges to the Lab ManagerEnsure conformance to the External Quality Assurance programIdentify and communicate trends in quality of lab testing or control proceduresAssist with staff training (and retraining) where error trends are identifiedAttend to audit reports and effectively implement corrective action and future preventative measuresIdentify and develop new SOPs for new studies according to study protocols as per lab manager/project manager requestReview SOPs as required and ensure SOP file is updatedEnsure lab documentation filing is up to date and audi
https://www.executiveplacements.com/Jobs/M/Medical-Technologist-Clinical-Pathology-WITS-RHI-1195560-Job-Search-06-18-2025-00-00-00-AM.asp?sid=gumtree
10mo
Executive Placements
1
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Key Performance Areas- Communicate any nonconformances for materials that do not meet specifications- Ensure that quality standards are always adhered to- Responsible for sampling and testing of all incoming materials according to the relevant procedures - Ensure all equipment is calibrated, in good working order and documents are recorded correctly- Ensure all deliveries are accompanied with the relevant documentation - Manage the printing of labels pertaining to all incoming goods (on hold, released, rejected) - Complete and file test schedules as per the analysis number; - Manage the approval of positives for the Bottle Printing department - Ensure that the version code is correct for all approved print artwork- Test packaging materials against specifications in order to release materials on time- Keep abreast with changes to specifications and regulations for packaging materials- Complete all relevant documentation regarding the testing of packaging materials- Report any rejections pertaining to packaging material to the,QC Manager- Ensure the batch number of products, GRN and COA correspond to packaging materials received- Ensure ISO standards are implemented and maintained Follow Good Manufacturing Practice (GMP) in the laboratory and in all areas of work- Ensure work area is always kept clean and tidy- Maintain cleanliness of the laboratory and production floors to minimise waste.Requirements- A minimum requirement of a technical qualification (NQF 4 5) will be preferred. - Prior knowledge of ISO/GMP/HACCP standards needed. - Intermediate level of computer literacy is required. - 2 3 years experience in a laboratory. - The ideal candidate will display excellent attention to detail and problem-solving abilities. - Ability to work independently and display excellent influencing and communication skills (verbal and written).
https://www.jobplacements.com/Jobs/L/Lab-Assistant-1197802-Job-Search-06-26-2025-04-12-22-AM.asp?sid=gumtree
9mo
Job Placements
1
Qualifications Matric Duties / Requirements Quality Control & TestingPerform quality checks on all raw materials before release for manufacturingInspect and approve all packaging materials, including cans, boxes, and lidsCheck grind quality of paste productsConduct quality checks on toners, including:ViscositySpecific gravity (density)ColourGlossDrying timeComparison against approved company standardsPerform quality checks on body fillers and putties, including:Gel timeSandabilityPinholes and cracksMonitoring the manufacturing process during productionCheck filling weights before filling starts and perform cross-checks during fillingInspect damaged packaging materials before disposalConduct quality checks on internally manufactured cansCustomer Returns & InvestigationsInspect customer return products by:Application and sprayingComparing results with retained samples and approved standardsReport findings clearly to managementLaboratory Trials & DevelopmentConduct manufacturing lab trials as per Managements instructions and report any issues or questionsPerform lab trials for new formulationsDecant and review old lab samples every 36 months and return acceptable material to productionMaintain a confidential formulation record book for all lab trialsData Entry & DocumentationEnter daily production data accuratelyRecord data for:Raw materials received from local and international suppliersRaw materials issued from warehouse for testingMaintain Excel reports for:All laboratory testsQuality inspectionsLab trials and resultsKeep monthly records of:Drawdown cardsSample cans usedReporting & CommunicationSend professional emails related to laboratory and quality activitiesProvide daily activity reports detailing work completed and observationsLaboratory Maintenance & HousekeepingMaintain high standards of laboratory housekeeping, including:Cleaning, mopping, and dustingKeeping the lab area organized and safeChange water in the spray booth every two weeksEnsure all laboratory equipment is clean, calibrated, and well maintainedConfidentiality & ComplianceMaintain strict confidentiality of all formulations, test results, and laboratory dataFollow all company safety, quality, and operational procedures
https://www.executiveplacements.com/Jobs/L/Laboratory-Technician--Quality-Control-1272487-Job-Search-03-17-2026-04-26-04-AM.asp?sid=gumtree
16d
Executive Placements
1
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Job Description:Conduct and oversee testing for production, R&D, and client samples.Oversee staff performance and ensure safety, quality, and compliance.Maintain and calibrate lab equipment; manage consumables and flammable materials.Lead improvements in lab processes, SOPs, and documentation systems.Handle SDS, TDS, and COA creation and updates for produced and supplied products.Manage retention samples, labeling systems, and BOM database updates.Deliver reports and technical support to internal departments and clients. Desired Experience & Qualification:B.SC or BTech in Chemistry Experience:35 years in a petroleum/lubricants lab environment with proven testing experience Required Skills:Strong interpersonal, communication, analytical, and problem-solving skillsMicrosoft Office and Windows proficiencyAbility to manage teams and work independentlyAbility to work under pressure Specialised knowledge:Lubricant/petroleum product testingFamiliarity with tribology, Sage Evolution BOM, Bartender Label Designer, and customer support. Direct Reports:Two Laboratory Technicians
https://www.executiveplacements.com/Jobs/T/Trainee-Laboratory-Manager-1196192-Job-Search-06-20-2025-04-23-19-AM.asp?sid=gumtree
9mo
Executive Placements
Technologist – Bacterial Laboratory – Own Car Female plant Pathology (preferred), Microbiology, Bioc
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TECHNOLOGIST – BACTERIAL LABORATORY – Own vehicle essentialRoodeplaat, PretoriaStart Date: 1 May 2026 (earlier start advantageous)Permanent | Post Level 10 (Peromnes)Own vehicle essential – SAQA Plant pathology preferred
qualification. Salary:R480 960 CTC per annum during probationR534 400 CTC upon successful completion of probation Minimum Requirements · SAQA
recognised tertiary qualification in Plant Pathology (preferred), Microbiology,
Biochemistry or related field · Experience
working in an ISO/IEC 17025:2017 accredited laboratory · Experience
with PCR diagnostics, ELISA and microbiological testing · Practical
laboratory analysis experience Key Responsibilities · Detection of
bacterial pathogens in crops · Conduct PCR,
ELISA and microbiological assays · Ensure
compliance with ISO/IEC 17025 quality systems · Supervise
laboratory assistants and support staff · Maintain
laboratory equipment and testing records · Participate
in proficiency and inter-laboratory testing · Authorise and
interpret laboratory test results Email updated WORD CV
and attach your current head and shoulders corporate photo to: jeansibanda@yahoo.com
or topnotch@telkomsa.net
18d
VERIFIED
1
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Minimum requirements: BSc in Chemistry or equivalent 5+ years QC experience in a laboratory environment or similar Solid experience with 18F FDG Quality ControlBackground in radiopharmaceuticals would be highly advantageous Consultant: Chante Du Toit - Dante Personnel Centurion
https://www.jobplacements.com/Jobs/Q/Quality-Control-Manager-1276245-Job-Search-03-29-2026-10-35-42-AM.asp?sid=gumtree
3d
Job Placements
1
We are looking for an Instrumentation Sales Representative (Carbon/Sulfur Instruments & Analytical Laboratory Equipment) based in Midrand The Instrumentation Sales Representative is responsible for driving sales growth, market expansion, and customer support for carbon/sulfur analysis instruments and related analytical laboratory equipment. This role combines technical expertise with strong commercial acumen to support clients in mining, metallurgy, chemicals, environmental labs, research institutions, and industrial manufacturing.The ideal candidate has a technical background in analytical instruments, excellent relationship-building skills, and the ability to translate complex technologies into clear value propositions.Key ResponsibilitiesSales & Business DevelopmentIdentify, pursue, and close new business opportunities for carbon/sulfur analyzers and complementary analytical instruments.Develop and execute territory sales strategies to achieve revenue targets.Conduct product demonstrations, presentations, and technical discussions with customers.Manage the full sales cycle: prospecting qualification solution proposal quotation negotiation order closure.Required Qualifications & ExperienceDiploma or Degree in Chemistry, Analytical Science, Metallurgy, Chemical Engineering, or related field.25+ years experience in technical sales of analytical instruments (preferably elemental analysis, spectroscopy, or laboratory equipment).Strong understanding of carbon/sulfur analysis, combustion analysis, or related methodologies.Valid drivers license and willingness to travel.Preferred Experience Previous experience selling carbon/sulfur analyzersExposure to mining, steel manufacturing, petrochemicals, cement, or environmental sectors.
https://www.jobplacements.com/Jobs/I/Instrumentation-Sales-Rep-Carbon-sulfide-instrumen-1257233-Job-Search-03-28-2026-00-00-00-AM.asp?sid=gumtree
5d
Job Placements
1
Division: Wits Mycology Main purpose of the job:To conduct research and to provide scientific support for research projects in order to fulfil the research mandate of Wits MycologySpecific responsibilities will include cryptococcal antigen testing, Histoplasma antigen testing and real time PCROther responsibilities will include performing laboratory testing for the COMBAT Candida program of workLocation:1 Modderfontein Road, Sandringham, JohannesburgMore info:Wits Mycology aims to improve the outcomes of people with varied lived experiences who are affected by life-threatening or disabling fungal diseases through clinical trials, observational studies, social science studies, and laboratory research and innovationOur research also stretches to other important infectious diseases We work in South Africa, across the African continent and globallyKey performance areas: To perform ethical and relevant research (basic and applied) that will provide new information on human diseases or disease-causing agentsTo apply specialised knowledge and provide interpretation of resultsTo evaluate and implement appropriate tests relevant to the activities of the Mycology division including assay design, laboratory testing, data entry, data management, data cleaning, data analysis and report-writing/ publishing in scientific journalsTo contribute to the teaching of students (from NHLS or academic institutes), health professionals and technical staff in research skills in order to develop research capacityTo write and submit research grant proposals to further the research capacity of the Mycology divisionhttps://www.jobplacements.com/Jobs/M/Medical-Scientist-Mycology-9-Months-Contract-Wi-1275597-Job-Search-03-26-2026-04-34-28-AM.asp?sid=gumtree
7d
Job Placements
1
Main purpose of the job:To provide best practice, data collection, clinical assessments, collection of specimens (cord and maternal blood) according to different study protocolsLocation:7 Esselen Street, Hillbrow, Johannesburg (CMJAH)Key performance areas: Inform participants about the studyVerify consent status prior to conducting any study proceduresDraw blood, cord blood from participants and maternal serum samples, process samples as required and specified within the protocol and laboratory manuals and send samples/specimens to laboratory OR ensure they are properly storedBiological sample collection as per study requirement other than blood samples, if applicableObtain vital signs and other special investigations as per study guidanceConduct pre and post HIV and Hepatitis B Test Counselling (if neededProvide appropriate health education and counselling where necessaryCommunicate participant management to site based staff in a timely manner adhering to ALOCOA principlesPerform tasks based on the protocol training provided and take accountability for self-training and documentation of this trainingCollect participant data from medical notes and complete source documentDocument necessary procedures, sample collection and data collection details in relevant source documents adhering to GCP principlesCompletion of source documents accurately and in a timely mannerMaintain full clinical records for all participantsMaintain an adequate inventory of laboratory samples (both electronic and hard copy, as required)Perform sample related activities
https://www.executiveplacements.com/Jobs/R/Research-Nurse-Night-Shift-3-Months-Temp-Contract--1275596-Job-Search-03-26-2026-04-34-28-AM.asp?sid=gumtree
7d
Executive Placements
1
ELECTRICAL MANUFACTURINGCertification & Laboratory EngineerR&DThe Area The Client is a leader in outdoor lighting world-wide whose mission is to provide cost-effective lighting solutions for safe, comfortable, and sustainable environments. The Certification & Laboratory Engineer position will form part of the Research and Development (R&D), based at Head Office in Olifantsfontein.Job PurposeResponsible for ensuring that all products comply with the requirements of national and international standards. To plan, direct and coordinate the testing of luminaires to ensure maintained compliance with relevant standards. This specifically includes the testing of luminaires used in explosive atmospheres.Content of the mission Product Certification - SABS and CERTEXEnsure that all new and existing models of products are tested by an accredited test laboratory and that products comply with the requirements of the relevant standards. Retention and maintenance of product certification test records and capturing them on the CLIENT- CLIENT intranet system.Liaise with the SABS Certification Department and CERTEX regarding the sampling and testing of post-permit samples and the carrying out of external post-permit audits.Testing of luminaires to specific permit conditions - SABS and CERTEXEnsure that luminaires are tested internally in accordance with the requirements of specific permit conditions (SABS and CERTEX certification) to verify compliance with the requirements of relevant specifications. Liaison with CERTEX with regards to change to design in Ex luminaires as defined in the type test report, ensure updating of the quality system and maintaining a system for categorizing updates, authorizing of initial approval and changes to relevant drawings, registering and control of drawings, authorizing of concessions, informing clients of any applicable special conditions for safe use and any schedules of limitations of luminaires used in explosive atmospheres. Responsible to ensure that all the necessary documentation accompanies the delivery note (IA Certificate, CERTEX certificate, CLIENT- CLIENT certificate with luminaire serial numbers, luminaire drawing). Ensure that unique serial numbers are applied to all luminaires and that the client acknowledges the receipt of the documents by signing the delivery note. Conducting general safety tests on luminaires governed by the relevant national and international standards, coordinating the drawing and testing of samples from production/stores to verify compliance with the requirements of standards and formally keeping record of all test results. Testing of luminaire componentsConducting tests on new components for po
https://www.executiveplacements.com/Jobs/C/Certification-and-Laboratory-Engineer-Electrical-M-1204285-Job-Search-07-18-2025-02-00-13-AM.asp?sid=gumtree
9mo
Executive Placements
1
Main purpose of the job:To assist with different aspects of research, laboratory processes, data collection, collation, and report writingLocation:NICD Modderfontein Road, SandringhamKey performance areas: Assessing study participation eligibilityUpdating of study specific control sheetsRegistration of samples on the laboratory information system or other study specific softwareDocument and track project plans and milestonesAttendance of meetings as and when requiredMaintain source document templates and make corrections to source templates as and when required by PI and/or monitorSupport different sections within the centre i.e. labelling, data entry, supplies, filing and storage etc.Process samples according to SOPs and study requirementsReport writingPlanning and prioritising the study needs and requirementsMinute taking during study meetingsIdentify processes for improvement and work with supervisor to initiate process improvement projectsTake ownership and accountability for tasks & activities and demonstrates effective self-managementFollow through to ensure that quality and productivity standards of own work are consistently and accurately maintainedInform relevant parties in the event of tasks or deadlines not met and provides appropriate means of resolutionMaintain a positive attitudeRespond to queries timeouslyWilling to help
https://www.jobplacements.com/Jobs/R/Research-Assistant-x1-12-Month-Fixed-Term-Wits-NIC-1276445-Job-Search-03-30-2026-04-35-52-AM.asp?sid=gumtree
3d
Job Placements
1
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Minimum Requirements:Must have a minimum of 2 to 3 years experience as a Quality Controller in the Plastics Manufacturing IndustryRelevant Quality or Laboratory Qualification requiredProficient in MS Office essential Strong knowledge of plastics testing methods, quality control processes and laboratory procedures will be beneficial Valid Drivers License and own Transport requiredContactable references and payslips requiredSalary Structure:Basic Salary negotiable based on experienceBenefits(Only suitable candidates will be shortlisted and contacted within 14 days)
https://www.jobplacements.com/Jobs/Q/Quality-Controller-1273373-Job-Search-03-19-2026-04-25-49-AM.asp?sid=gumtree
14d
Job Placements
1
Minimum requirements for the role:A minimum Grade 12 is essential for this role.The company is happy to train a matriculant with no experience for this role.The successful candidate should be mechanically and technically inclined and keen to work within the medical/diagnostic industry.Must be able to communicate well, work independently or in a team under pressure, and follow instructions.The successful candidate will be responsible for:Supporting the production and stores operations, ensuring smooth workflow, equipment functionality, and adherence to quality standards for diagnostic/medical media within the industry.Assisting with production tasks in the medical/diagnostics environment, including sample handling, preparation, and packaging.Maintaining and troubleshooting laboratory and production equipment to ensure operational efficiency.Monitoring equipment performance and reporting technical issues promptly.Managing inventory and storage of consumables, reagents, and packaging materials.Organising stock levels, performing regular counts, and assisting with procurement requests.Receiving and inspecting deliveries to ensure compliance with quality standards.Performing basic maintenance and repairs on laboratory and production equipment under supervision.Applying mechanical and technical knowledge to solve problems quickly and efficiently.Maintaining accurate records of production activities, stock movements, and equipment maintenance.Prioritising tasks to meet deadlines and production schedules.Salary package, including benefits, is highly negotiable depending on experience gained.
https://www.jobplacements.com/Jobs/P/Production-Stores-Assistant-Medical-Diagnostics-Eq-1274962-Job-Search-03-24-2026-10-35-55-AM.asp?sid=gumtree
8d
Job Placements
1
Minimum requirements for the role:A bachelors degree/ diploma or equivalent in a relevant field (e.g., Chemistry, Biochemistry, Life Sciences), sales training is essential for this role.Previous sales experience selling products within the laboratory industry is preferred. Must have a strong background in laboratory operations and Point of Care.Must be computer-literate in the Microsoft Office suite applications or similar.Must be able to work on CRM systems and be able to populate data and customer information.The successful candidate will be responsible for:Achieving the companys strategic objectives by growing and driving sales by promoting life sciences and clinical diagnostic products and services to Key Accounts and New Customers. Presenting and selling a range of products and services to current Key Accounts and new clients.Preparing action plans and schedules maintaining and finding ways to improve forecasting accuracy by securing customer forecasts.Managing short-and long-term growth objectives with customers.Preparing and presenting presentations, proposals, and sales quotes.Creating weekly pre-call plans for customer visits with clear objectives and an agenda.Prioritising customer satisfaction by understanding their unique requirements and delivering tailored solutions.Establishing and maintaining current client and potential client relationships.Managing account services through quality checks and with additional follow-up and customer meetings.Participating in marketing events such as conferences, seminars, trade shows, and industry events.Ensuring good market penetration by utilising effective go-to-market strategies.Collaborating with Supply Chain and Customer Service to ensure operational excellence.Collaborating closely with the Quality Manager and Regulatory Affairs teams to ensure all products comply with applicable regulatory requirements and quality standards.Preparing, compiling, and submitting regulatory documentation required for product registrations and approvals.Salary package, including benefits, is highly negotiable depending on experience gained.
https://www.executiveplacements.com/Jobs/R/Regional-Sales-Representative-Clinical-Diagnostic--1277903-Job-Search-04-02-2026-10-37-28-AM.asp?sid=gumtree
10h
Executive Placements
1
The Quality Control Manager to complete and oversee routine testing and analysis for the laboratory including the production of standard 18F synthesis and other tracers in strict adherence to Good Manufacturing Practices (GMP), relevant European Union (EU) and United states (USP) pharmacopoeia standardsManage raw material sampling, testing and release systemEnsure efficient performance of, and undertake first-line maintenance of, Quality Control equipment including: - High Performance Liquid Chromatography (HPLC), Chromatography (radiochemical and chemical purity of 18F FDG) , Gas Chromatography, pH measurement, Radio Thin Layer Chromatography (RTLC), Gamma Spectrometer Limulus Amoebocyte Lysate (LAL) testingMaintain records of faults, maintenance, and calibration on any dysfunction, operation or equipmentIn association with the RP and Quality Assurance team to develop, implement and manage cGMP, Quality Control and Quality Assurance systems and procedures for standard tracersManagement of QC raw material and consumables, formulation of reagents for radiochemistry, mixing of solvents for HPLC and other analyses, cleaning of glassware and disposal of waste chemicals and materialsPrepare updated SOPs in accordance with the relevant guidelines as may be necessary from time to time for approval by the RP and adoption by the groupProvide training and support for others selected as backup in undertaking routine QC operationsMaintain understanding of best practice and changes in requirements for QC analytical testingUndertake training as a Radiation Protection officer (RPO) to safely undertake the routine manufacturing of radiopharmaceuticals and the disposal of radioactive wasteStrictly adhere to GMP, Good Laboratory Practice (GLP) and safety protocols laid down by SAHPRA, in accordance with issued licenses as determined by Quality assurance pharmacist time to timeCorresponding and adherence to local rules developed to ensure conformity to such licensing requirementsExperience requiredQuality control experience required 4 - 5 yearsManagerial experience will be advantageousSkills and CompetenciesWorking effectively with members of the teamExcellent interpersonal skillsExcellent organisational skillsAttention to detailGood listening skillsSelf-motivatedAble to work independently and effectively by completing tasks in a timely mannerQualificationsBSc / B.Tech or similarQualifications in radiopharmaceutical chemistry laboratoryExperience in 18F FDG Quality Control
https://www.jobplacements.com/Jobs/J/Junior-QC-Manager-Radiopharmaceuticals-1274040-Job-Search-03-20-2026-10-19-54-AM.asp?sid=gumtree
12d
Job Placements
1
In this role, you will:Provide technical expertise and support for our advanced pyrometers, line scanners, and thermal imaging systems.Help clients improve product quality, boost production, and enhance process efficiency.Ensure seamless integration and long-term reliability of our solutions, calibrated in ISO17025-certified laboratories.Support industries ranging from sustainable steelmaking, glass, mining to electric vehicle battery production.Key ResponsibilitiesDeliver technical support and product demonstrations to customers.Collaborate with sales and engineering teams to design and implement solutions.Maintain up-to-date knowledge of industry trends and Proteas product offerings.Build and maintain strong client relationships.RequirementsTechnical qualification or relevant plant experience (essential).Knowledge of industrial automation.Client-driven and customer-focused mindset.Sales or plant experience in one or more of the following:Infrared non-contact temperature measurementTemperature, level, flow, or pressure measurementField measurementNote: SCADA or PLC experience is not required.What We OfferMarket-related salary, commensurate with experience.Open-ended commission scheme based on sales margin.Motor vehicle and fuel allowance.Pension and medical aid.Ongoing training and development opportunities.
https://www.executiveplacements.com/Jobs/I/Industrial-Instrumentation-Product-Specialist-1273302-Job-Search-03-19-2026-04-08-20-AM.asp?sid=gumtree
2d
Executive Placements
1
RedCat Recruitment is seeking an experienced PLANT MANAGER (MANUFACTURING / PRODUCTION) for a large international concern. Position based in the Sundra area, Mpumalanga. JOB DESCRIPTIONGrade 12.Degree in Industrial Engineering.English / Zulu speaking person.Valid Code 08 drivers license / own reliable vehicle.Competent computer skills (MS Office, Email / Internet).2 - 5 years experience in a similar position.Person will be required to oversee and manage the operational activities of the factory and site on a daily basis. To ensure that all company requirements on HR, quality, safety, risk, environment, administration, logistics and production are met within the production environment.Complying with health, safety and risk regulations.Environment and sustainability.Leadership and human resources.Quality and laboratory.Finance and administration.Procurement and inventory.Operations management.Business intelligence and communication. Salary package offered: - To be discussed PLEASE ONLY APPLY IF YOU HAVE THE RELEVANT EXPERIENCE / ONLY SUITABLE CANDIDATES WILL BE CONTACTED. IMPORTANT
https://www.executiveplacements.com/Jobs/P/PLANT-MANAGER-MANUFACTURING-PRODUCTION-1274620-Job-Search-3-24-2026-5-19-11-AM.asp?sid=gumtree
9d
Executive Placements
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