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Results for pharmaceutical manufacturing in "pharmaceutical manufacturing" in South Africa in South Africa
1
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Key performance areas will include, but are not limited to:Identifying, validating, and implementing QC analytical methods and equipment/systemsInvestigating QC incidents and out-of-specification resultsMonitoring and reporting performance of inhouse controls and reference standardsImplementing and maintaining a competency-based cGMP training system that meets business and regulatory requirementsExecuting of training related administrative requirements independently and in conjunction with relevant stakeholders where requiredQuality Assurance general supportKey Requirements: A relevant qualification in Quality or cGMP and/or a relevant training qualification with at least 5 years experience in a pharmaceutical manufacturing or quality assurance environment, with working knowledge of cGMP, pharmaceutical facilities, processes, equipment, and systems. Additionally the candidate should have at least 2 years experience in a training role and possess knowledge of adult learning theory, instructional design, and effective training methodologies. Post Basic Pharmacist Assistant qualification preferred.Additional Requirements: Computer literacy, excellent verbal and written communication skills, strong independent/cross-disciplinary skills, attention to detail, and good interpersonal communication and presentation skills with personnel from multiple departments and employee levels.*Only candidates that meet all the requirements should apply**Only candidates that are shortlisted will be contactedBy sending your application to Scistaff you consent that your information may be kept in accordance with the requirements of the POPI Act.
https://www.jobplacements.com/Jobs/G/GMP-Training-Officer-1255315-Job-Search-04-01-2026-00-00-00-AM.asp?sid=gumtree
3d
Job Placements
1
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Minimum requirements: Confident in managing and motivating a team of seven QA professionals, including a QA Manager, QA Pharmacist, Regulatory Affairs Officer, Administrator, and Compliance staffHolds a Degree or Diploma in Chemistry, Biochemistry, Microbiology, or a closely related scientific fieldBrings at least 5 years of hands-on experience in an analytical lab environment within the cosmetics or pharmaceutical sectors, with a minimum of 12 years in a leadership or supervisory capacityKey Competencies & Strengths:Strategic Supply Chain Oversight: Skilled in leading supply chain operations with a strategic approach, ensuring that planning and procurement are aligned with overall business objectivesDemand Planning & Forecasting Expertise: Experienced in driving demand planning accuracy and production forecasting, particularly in fast-paced, high-volume manufacturing settingsSupplier Management & Contract Negotiation: Demonstrated ability to source, evaluate, and negotiate with suppliers to consistently achieve targets related to quality, cost, and timely deliveryERP & Inventory Systems Proficiency: Well-versed in ERP platforms such as SAP, Syspro, or similar, and experienced in using WMS to manage stock, streamline planning, and optimise inventory levelsRegulatory & GMP Compliance: Deep understanding of GMP and regulatory standards applicable to FMCG, pharmaceutical, or cosmetics industries, with a focus on audit readiness and quality controlData-Led Decision Making: Strong analytical thinker who leverages KPIs and performance data to drive continuous improvement, operational efficiency, and cost reduction Consultant: Debbie Watkyns - Dante Personnel Cape Town
https://www.executiveplacements.com/Jobs/Q/QUALITY-ASSURANCE-QC-SUPERVISOR-1198259-Job-Search-06-27-2025-04-34-36-AM.asp?sid=gumtree
9mo
Executive Placements
1
Salary: R84,000 per month (CTC) Our client, a highly reputable and well-established company in the pharmaceutical industry, is seeking a mature, experienced, and detail-oriented Regulatory Affairs and Responsible Pharmacist to join their team in Johannesburg.Key Duties & ResponsibilitiesCompany ComplianceEnsure full compliance with SAPC, SAHPRA, and DOH legislation.Operate in line with the Medicines and Related Substances Control Act and Pharmacy Act.Manage printed packaging and promotional material compliance.Oversee Quality Management System including SOP implementation, updates, and audits.Coordinate with local laboratories for Post Importation Testing.Approve and release product batches for market in line with regulatory requirements.Maintain and update the Site Master File, SOPs, and Quality Manual.Prepare for and support SAPC/SAHPRA inspections.Ensure adequate training and documentation of staff competency.Review and approve batch manufacturing documentation prior to production.Product RegistrationCompile, screen, and submit new registration applications to SAHPRA.Handle registration-related queries and maintain partner communication.Submit product variations and renewals as per SAHPRA requirements.Stay updated with local legislative changes and ensure ongoing compliance.Submit regulatory dossiers using Docubridge eCTD.Documentation & Quality ManagementManage the regulatory document control system.Ensure retention and availability of regulatory and quality records.PharmacovigilanceMonitor and manage all adverse drug reactions across the group.Ensure timely receipt, review, and appropriate responses.ReportingProvide weekly project updates to the CBDO and CEO.Minimum RequirementsBPharm Degree5+ years experience in Regulatory AffairsPrevious experience as a Responsible PharmacistProven experience in Quality AssuranceBehavioural & Technical CompetenciesHigh integrity, ethical, and confidentialAccountability and ownership of complianceStrong leadership and interpersonal skillsExcellent communication and planning abilityExceptional attention to detailConscientious, cooperative, assertive
https://www.executiveplacements.com/Jobs/R/Regulatory-Affairs-and-Responsible-Pharmacist-1198089-Job-Search-6-27-2025-7-00-20-AM.asp?sid=gumtree
9mo
Executive Placements
1
Key Responsibilities:Manage the full accounting function up to trial balancePrepare accurate monthly management accounts and variance analysesOversee reconciliations for debtors, creditors, bank, and general ledger accountsMaintain fixed asset registers in line with company policiesSupport month-end, quarter-end, and year-end processesAssist with financial audits and ensure that all documentation meets pharma compliance standardsMonitor cost controls and assist with budgeting and forecastingEnsure that financial records align with pharmaceutical industry regulations and internal SOPsWork closely with supply chain and operations to track stock, costing, and batch-related financial dataMinimum Requirements:BCom Accounting degree (or equivalent)Completed SAICA or SAIPA articles13 years postâ??articles experienceExperience in the pharmaceutical, FMCG, manufacturing, or similar regulated environment advantageousStrong understanding of accounting principles and internal controlsAdvanced Excel and experience with major accounting systemsHigh attention to detail and strong problem-solving skillsCompetencies:Analytical and deadlineâ??drivenAbility to work under pressure in a compliance-focused environmentStrong communication skills and professional approachEthical, accurate, and quality-focusedð??§ Apply now!For more exciting Finance
https://www.executiveplacements.com/Jobs/A/Accountant--Pharmaceutical-industry-1274726-Job-Search-03-24-2026-00-00-00-AM.asp?sid=gumtree
8d
Executive Placements
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1. Pharmaceutical Supply Services
Supply of pharmaceutical excipients
Provision of laboratory reagents and chemicals
Supply of consumables (filters, syringes, vials, tubing, PPE, etc.)
Sourcing of specialty and hard-to-find pharmaceutical products2.Supply of bulk industrial chemicals
Supply of solvents (analytical & industrial grade)
Supply of cleaning and sanitation chemicals
Water treatment chemicals
Construction and process chemicals
Customized sourcing for manufacturing and processing industries3. Laboratory & Pharmaceutical Equipment Supply
Supply of laboratory instruments
Cleanroom equipment (e.g., laminar airflow cabinets, particle counters)
Manufacturing equipment (mixers, filling machines, pumps)
Analytical instruments (pH meters, balances, spectrometers)
Temperature and environmental monitoring systems
Installation support and commissioning4. Engineering Consultancy Services
Facility design & layout
GMP-compliant cleanrooms
Sterile and non-sterile compounding labs
Process design & optimization
Utilities design
HVAC systems
Water systems (PW, WFI)
Compressed air systems
Project management
From concept to commissioning
Equipment selection & specification
Turnkey project solutions5. Validation & Qualification Services
IQ (Installation Qualification)
OQ (Operational Qualification)
PQ (Performance Qualification)
Process validation
Cleaning validation
HVAC validation
Computer system validation (CSV)6. Regulatory & Compliance Support
GMP compliance consulting
SOP development
Audit readiness and gap analysis
Documentation systems implementation
Quality Management System (QMS) setup7. Maintenance & Technical Support
Preventive maintenance programs
Equipment calibration services
Troubleshooting and repair support
Spare parts sourcing8. Procurement & Sourcing Services
Global sourcing of pharmaceutical and industrial materials
Supplier qualification and auditing
Cost optimization and vendor negotiation
Import/export coordination9. Training & Technical Support
GMP training
Cleanroom behavior training
Equipment operation training
Quality and compliance workshopS10. Specialized Services (Value-Added)
Turnkey setup of pharmaceutical facilities
Support for start-ups entering pharma manufacturing
Custom solutions tailored to client operations
15d
Randburg1
Our client is a specialist air quality and cleanroom services provider supporting highly regulated environments. They work closely with pharmaceutical manufacturers, medical laboratories, and healthcare facilities to ensure compliance with international cleanroom and air quality standards. The company is known for its technical expertise, hands-on approach, and long-term client partnerships.The role involves conducting cleanroom and air quality validations at client sites, including filter integrity testing, air velocity and volume measurements, airborne particle counting, and recovery testing. The successful candidate will analyse results, ensure compliance with relevant standards, and compile accurate technical reports for clients while maintaining testing equipment and professional client engagement.Job Experience and Skills Required:Relevant technical qualification (Mechanical, Electrical, HVAC, or similar)Experience within pharmaceutical, medical laboratory, or cleanroom environmentsHands-on exposure to cleanroom validation or air quality testingProficient in Microsoft Excel for data capturing and reportingValid drivers licence and willingness to travel to client sitesApply now!
https://www.executiveplacements.com/Jobs/C/Clean-Room-Air-Quality-Testing-Technician-HVAC-1257663-Job-Search-03-19-2026-00-00-00-AM.asp?sid=gumtree
1d
Executive Placements
1
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The ARM Quality Manager reports to the Head: Quality Management and Scientific Affairs and will be responsible for contributing to the quality, safety, and efficacy of the companyâ??s products through rigorous evaluation and approval of new plasma suppliers in line with the companyâ??s specifications and local and international guidelines; reviewing epidemiological data and other data from plasma suppliers and updating the companyâ??s plasma master file on an annual basis; testing and releasing of human plasma and its derivatives (active raw materials) procured from plasma suppliers, adhering to sound scientific principles and complying with current good manufacturing practice (cGMP); being responsible for the smooth, efficient day-to-day operation of the Quality Active Raw Material (QARM) laboratory, providing operational assurance in support of business and strategic requirements; and being responsible for the companyâ??s formal environmental monitoring program, through monitoring production environments, including the aseptic filling suite, ensuring the environments comply with regulations.Key Requirements:Â MSc in Microbiological Science, Molecular Biology, Biochemistry, or a related field, with a PhD degree preferred. A minimum of 5 yearsâ?? experience in quality Control or a Microbiological laboratory and 5â??10 yearsâ?? experience as a senior staff manager in a quality or pharmaceutical environment. Working knowledge of GMP in blood establishments, transfusion transmittable infections, plasma quality and safety, and related regulatory requirements; a thorough understanding of cGMP, GLP, and international pharmaceutical standards preferred; and hands-on experience with internal and supplier audits will be advantageous.Additional Requirements:Â Strong oral and written communication, people managements and development, problem solving, quality awareness, attention to detail and analytical, quantitative analysis, relationship management, and personal leadership skills. Additionally, the ideal candidate should have statistical knowledge, the ability to work independently, but also in a team, and business impact.*Only candidates that meet all the requirements should apply**Only candidates that are shortlisted will be contacted By sending your application to Scistaff you consent that your information may be kept in accordance with the requirements of the POPI Act.
https://www.executiveplacements.com/Jobs/A/Active-Raw-Material-Quality-Manager-1245530-Job-Search-03-29-2026-00-00-00-AM.asp?sid=gumtree
5d
Executive Placements
1
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This opportunity is based at a highly respected international healthcare manufacturing organisation, known for producing advanced medical and pharmaceutical solutions supplied to hospitals, clinics, and patients across the globe.You will play a central role in coordinating production-related financial processes, ensuring accurate costing, stock control, and reporting within a fast-paced factory environment in Modderfontein. This position suits a detail-driven professional who understands the financial mechanics of manufacturing operations and thrives on systems, controls, and continuous improvement.Key responsibilities include:Coordinating production costing, variance analysis, and manufacturing financial reportingSupporting stock control processes, reconciliations, and bill-of-materials accuracyWorking closely with production, supply chain, and finance teams to ensure aligned planning and reportingMaintaining accurate system data and supporting month-end processesMonitoring production efficiencies and assisting with budgeting and forecasting inputsRequirements:Proven accounting or bookkeeping experience within a manufacturing environmentStrong understanding of costing principles and production finance controlsProficiency in SAP and Advanced Microsoft Excel (essential)Relevant finance qualification; CIMA advantageous but not essentialHigh attention to detail, structured working style, and ability to operate in a deadline-driven factory setting.The offer will be market related in line with your qualifications, skills, and experience. The role can offer up to R25 000 basic per month (with additional large company benefits) for candidates who are an exact fit and require minimal additional training or oversight.Please apply online in the link provided. We do not consider CVs via Whatsapp or email.
https://www.jobplacements.com/Jobs/J/Junior-Production-Coordinator-1273143-Job-Search-03-18-2026-10-29-31-AM.asp?sid=gumtree
11d
Job Placements
1
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Job Title: Quality Control (QC) Supervisor? Location: Parow, Cape Town? Full-time | Office-Based | Employment Equity RoleA well-established manufacturing organisation is looking for a qualified and experienced QC Supervisor to join their Quality team. This role requires strong leadership, quality control expertise, and familiarity with regulatory standards such as GMP and ISO.Key Responsibilities:Supervise and lead the QC team, including Analysts, Technicians, Samplers, and AdministratorsEnsure compliance with GMP, ISO, and internal quality standardsReview and approve lab data, test results, and quality documentationOversee routine inspections, instrument calibration, and troubleshootingInvestigate non-conformances in collaboration with QA, Production, and Technical teamsCoordinate with suppliers on packaging materials and specificationsDevelop and monitor QC procedures, sampling plans, and quality protocolsSupport production through in-process checks and environmental monitoringRequirements:Diploma or Degree in Chemistry, Biochemistry, Microbiology, or related fieldMinimum 5 years’ lab experience in cosmetics or pharmaceuticals1–2 years in a supervisory roleStrong working knowledge of GMP, GLP, ISO, and QMS standardsProficient in lab systems (e.g., Syspro) and quality control processesExcellent communication, problem-solving, and team coordination skillsIf you are q
https://www.executiveplacements.com/Jobs/Q/Quality-Control-Supervisor-1198044-Job-Search-06-27-2025-02-00-15-AM.asp?sid=gumtree
9mo
Executive Placements
1
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Duties & ResponsibilitiesAssemble complex mechatronic modules and systems in a controlled cleanroom environment to exacting quality standardsFollow technical drawings and production documentation to build mechanical, electrical, and pneumatic sub-assembliesPerform precision measurement and inspection using micrometers, calipers, and dial gaugesDocument all quality data and flag deviations proactivelyAdhere to strict cleanroom gowning and contamination control protocolsWork rotating morning and evening shifts with flexibility for overtimeContribute to lean manufacturing and continuous improvement initiativesExperience & QualificationsTechnical trade qualification in Mechanical Engineering, Mechatronics, Diesel Mechanics, Automotive Technology, or similar (N4N6 National Diploma, Red Seal Trade Certificate, or equivalent) or Aircraft Maintenance Engineer (AME) credentials.Hands-on experience assembling or disassembling complex mechanical systems, particularly engine rebuildsAbility to read and interpret engineering drawingsBackground in a regulated manufacturing environment (automotive OEM, aviation MRO, marine, pharmaceutical, or similar)Strong attention to detail and a team-player attitudeWillingness to relocate to The Netherlands
https://www.jobplacements.com/Jobs/C/Cleanroom-Assembly-Technician-1269754-Job-Search-03-20-2026-00-00-00-AM.asp?sid=gumtree
16d
Job Placements
1
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The successful candidate will support the full finance function and ensure accurate financial reporting, compliance, and operational support in a fastâ??paced and regulated VET environment.Key Responsibilities:Manage the full accounting function up to trial balancePrepare monthly management accounts, including variance analysisPerform and review debtor, creditor, bank, and general ledger reconciliationsMaintain and manage the fixed asset register in line with company policiesSupport monthâ??end, quarterâ??end, and yearâ??end close processesAssist with internal and external audits, ensuring compliance with VET industry standardsSupport cost control initiatives, budgeting, and forecastingEnsure financial records align with industry regulations, internal controls, and SOPsWork closely with operations and supply chain teams to monitor stock, costing, and product/batchâ??related financial dataMinimum Requirements:BCom Accounting degree or equivalentCompleted SAICA or SAIPA articles13 years postâ??articles experienceExperience in the VET, FMCG, pharmaceutical, manufacturing, or similarly regulated environment (advantageous)Solid understanding of accounting principles and internal controlsAdvanced Excel skills and experience with large accounting systemsStrong attention to detail and analytical problemâ??solving skillsKey Competencies:Analytical and deadlineâ??drivenAbility to work under pressure in a complianceâ??focused environmentStrong communication and stakeholder engagement skillsEthical, accurate, and qualityâ??focusedApply Now!ð??§ Ready to take the next step in your finance career? Apply today!For more exciting Finance vacancies, visit:ð??
https://www.executiveplacements.com/Jobs/A/Accountant--Veterinary-Industry-1276139-Job-Search-03-27-2026-00-00-00-AM.asp?sid=gumtree
6d
Executive Placements
25
R 6,500,000
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**Exceptional 2200m² Factory for Rent in Marlboro, Sandton**Discover a top-tier food-grade warehouse available for rent in the heart of Marlboro, Sandton. This outstanding facility is meticulously designed to meet the stringent requirements of businesses operating in the food and pharmaceutical sectors. Spanning three stories, the warehouse is equipped with a goods lift for efficient vertical transportation of goods. It features ISO paneling throughout, ensuring that the highest standards of hygiene and temperature control are maintained. The well-structured layout of the property supports seamless operations, aligning perfectly with food-grade compliance requirements.To further enhance its functionality, the facility includes a powerful 400kVA generator and a 500kVA incomer, ensuring uninterrupted operations. Multiple roller shutter doors provide excellent access for deliveries and dispatch, making it an ideal choice for manufacturing, storage, or distribution activities.Located in Marlboro, this property offers strategic access to major routes, including the M1 and N3 highways, facilitating easy connectivity to key business hubs. This is a rare opportunity to secure a premium industrial property within one of Sandton’s prime industrial nodes.Dont miss out on this exceptional offering. Click on the link for a video tour of the property and see firsthand what makes this facility stand out.Property Reference #: 2378027Agent Details:Sanele NgcoboSwindon Property - Gauteng2nd Floor, Building 16, The Woodlands Office Park, 20 Woodlands Drive, Woodmead, Johannesburg, 219
2mo
Swindon Property - Gauteng
1
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Our client is one of the leading sterile vaccine manufacturers rooted in Africa, with our core purpose being to protect life. We are looking to hire a dynamic, passionate, confident, proactive, and meticulous Head of People Operations to join a goal-oriented team.CORE ACCOUNTABILITY:To lead the execution of our human capital operations strategy across Africa. This pivotal role will drive operational excellence across the full employee lifecycle, ensuring a human centric, agile, data-driven people philosophy and infrastructure is in place, that positions our client as a biopharmaceutical employer of choice, and that is aligned with our mission to build a sustainable vaccine ecosystem for Africa. The incumbent acts as the strategic operational bridge between our clients’ long-term talent strategy and the everyday experiences that shape engagement, performance, and retention.QUALIFICATIONS NEEDED:Bachelors degree in human capital / human resources management or a related field.Postgraduate diploma in business management or Leadership preferred.Recognition of Prior Learning (RPL) will be considered for extensive practical experience.EXPERIENCE REQUIRED FOR SUCCESS:Minimum 10 years of progressive Human Capital generalist experience, including 4 years in a senior HC leadership role.Proven success in a manufacturing or life sciences environment, preferably pharmaceutical, biotech, or vaccine production.Strong track record in organisational development, people project management, workforce planning, talent mapping, career pathing, and employee engagement.Demonstrated local and continental labour relations and compliance management expertise, including policy development and dispute resolution.Experience in Payroll Management, HR systems scoping and implementation, analytics, and operational process optimisation.KNOWLEDGE AND SKILLS NEEDED TO MAKE A MEANINGFUL IMPACT:Deep understanding of South African Labour Legislation and pragmatic IR application.Knowledge of scarce skill attraction and retention strategies, particularly in technical and scientific fields.Advanced capability in HC policy, process design, and people metrics.Skilled in performance management, succession planning, and career development frameworks.Strong change management, stakeholder engagement, and communication capabilities.Digitally savvy with strong experience across established HR information & payroll systems and platforms as well as well-established across the full office 365 suiteKEY RESPONSIBILITIES OF THE ROLE: Strategic LeadershipAssist with developing and lead operationalisation of our client’s Human Capital Strategy through a forward-looking People
https://www.jobplacements.com/Jobs/H/HOD-People-Operations-1276321-Job-Search-03-30-2026-03-00-16-AM.asp?sid=gumtree
5d
Job Placements
1
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This innovative pharmaceutical manufacturing company is a key player in the vaccine production industry, committed to advancing public health through science, precision, and world-class manufacturing standards. With a strong footprint in the biotech and healthcare space, the business offers an exciting opportunity to take on a leadership role in a mission-driven environment.As the Finance Lead, you will report to the CFO and be responsible for the full finance function, from preparing annual financial statements and managing budgeting and forecasting cycles to ensuring compliance with IFRS and regulatory standards. You will oversee internal controls, manage banking relationships, and produce high-impact reports to support strategic decision-making. Managing a team of three direct reports, your leadership will be crucial in building a resilient, efficient, and insight-driven finance department.Job Experience and Skills Required:- Qualified CA(SA) with completed articles- Minimum 5 years post-articles experience in a full finance function role- Experience in a manufacturing or pharmaceutical/biotech environment is advantageous- Strong technical knowledge of IFRS and experience drafting annual financial statements- Proficiency in budgeting, forecasting, and financial reporting- Ability to design and implement financial controls and systems- Experience with SAP ERP system- Strong leadership skills and experience managing finance teamsApply Now!
https://www.executiveplacements.com/Jobs/F/Financial-Lead-1201954-Job-Search-07-10-2025-04-13-37-AM.asp?sid=gumtree
9mo
Executive Placements
1
Roles and ResponsibilitiesRole OverviewWe seek an experienced Production & Quality Control Supervisor to oversee operations at our soap bar manufacturing facility. This role ensures that all products meet internal and external quality standards while optimizing production processes.Key ResponsibilitiesProduction & Quality Assurance: Lead production staff to meet quality and efficiency targets. Implement and monitor quality assurance procedures, ensuring regulatory compliance.Process Improvement: Identify and implement enhancements to reduce defects, improve efficiency, and maintain high standards. Investigate and address customer complaints.Team Leadership & Training: Supervise, train, and mentor staff. Conduct root cause analyses for defects and implement corrective measures.Qualifications & ExperienceEducation: Matric with experience in Quality Control & Production Supervision. Certification in Quality Management (e.g., ISO 9001) is advantageous.Experience: 3+ years in quality control/assurance within cosmetics, toiletries, or pharmaceutical manufacturing. Proven leadership in supervising production teams.Skills: Strong problem-solving, analytical, and organizational abilities. Excellent communication and ability to perform under pressure.Personal AttributesStrong leadership and interpersonal skillsHigh integrity and commitment to qualityProactive, solution-oriented mindsetBenefitsCompetitive salary based on experienceDynamic, collaborative work environmentGrowth opportunities in a rapidly expanding companyIf you are a motivated leader passionate about quality and production efficiency, we encourage you to apply!Job Type: Full-timePay: R15 000,00 - R18 000,00 per monthEducation:High School (matric) (Required)Experience:Quality Control cosmetics/toiletries/pharmaceutical: 3 years (Required)Quality Control & Production Supervision: 3 years (Required)Certification in Quality Management (e.g. ISO 9001): 3 years (Preferred)Supervising production teams: 3 years (Required)Employment DetailsEmployment Type: Permanent EmploymentIndustry: PharmaceuticalWork space preference: Work OnsiteIdeal work province: GautengIdeal work city: Kempton ParkSalary bracket: R 15 000 - 18 000Drivers License: CODE B (Car)Own car needed: Yes
https://www.executiveplacements.com/Jobs/P/Production--Quality-Control-Supervisor-1201454-Job-Search-07-09-2025-04-06-50-AM.asp?sid=gumtree
9mo
Executive Placements
Jermaine Naidoo3 Viewside Road,Caneside | naidoojermaine02@gmail.com0817139209Dear hiring manager:I am a conscientious and disciplined hard worker, with the ability to work well as an individual or as a member of a team. I am very determined when faced with a new challenge and enthusiastic when learning new skills.Previous positions held in my working careerDespatch managerWarehouse manager Administration managerSectors fields worked inPlasticMedical/pharmaceutical Inks and graphics Clothing productionParty/decor Skills learnt over my working career▪Computer Literary (Proficient in MS Word, Excel, Emails and Internet)▪Customer Services▪Data Maintenance▪Omni accounts▪SAP software ▪Pastel Partner▪Administration ▪Ability to adapt to company software systems▪Warehouse Management ▪Receiving/Dispatching ▪Stock Control ▪Admin – Manager/Supervisor▪Fleet Control▪Staff Management For a much more detailed resume please kindly contact me on the above. Sincerely,Jermaine Naidoo
20d
Morningside1
Key ResponsibilitiesRegulatory AffairsEnsure compliance with applicable medical device regulations (e.g., SAHPRA, FDA, EU MDR, ISO 13485, ISO 14971).Prepare, submit, and maintain product registrations, licenses, and approvals with regulatory authorities.Monitor regulatory changes and advise management on potential impact to business and products.Support audits and inspections by regulatory authorities and notified bodies.Maintain technical documentation, regulatory files, and product labeling compliance.ComplianceDevelop, implement, and monitor compliance programs in line with company policies, codes of conduct, and industry standards.Conduct compliance risk assessments and recommend corrective actions.Ensure adherence to anti-bribery, anti-corruption, data privacy, and ethical marketing practices.Train staff on compliance policies, procedures, and ethical conduct.Investigate and report compliance breaches, ensuring timely resolution.Health & Safety (HSE)Develop and implement occupational health and safety programs aligned with local legislation (e.g., Occupational Health and Safety Act, ISO 45001).Conduct risk assessments, safety inspections, and incident investigations.Provide safety training and promote a culture of health, safety, and environmental awareness.Ensure safe handling, storage, and disposal of medical and hazardous materials.Maintain emergency response and business continuity plans. Qualifications & ExperienceBachelors degree in Regulatory Affairs, Quality Management, Life Sciences, Engineering, or related field.35 years experience in regulatory, compliance, or HSE role within the medical device, pharmaceutical, or healthcare industry.Strong knowledge of medical device regulations and standards (ISO 13485, ISO 14971, EU MDR, FDA, SAHPRA, etc.).
https://www.executiveplacements.com/Jobs/R/Regulatory-Compliance-and-Health--Safety-Officer-1273422-Job-Search-03-19-2026-04-38-36-AM.asp?sid=gumtree
16d
Executive Placements
1
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Job Title: Sales Representative Location: Cape Town, Killarney GardensJob Type: Full-TimeIndustry: Glass Packaging and ClosuresAbout Our Client:Our client has been in the bottling business since 1965 and has become a recognized leader in the Glass Packaging and Closures industry, offering high-performance solutions with outstanding clarity, durability, and functional design. Every product is subject to rigorous quality controls, ensuring clients receive consistent and premium-grade packaging across a wide range of sectors.Position Overview:Our client is looking for an experienced Sales Representative to drive business in the Glass Packaging and Closures industry space. The ideal candidate will have a deep understanding of the packaging industry and prior experience with other glass manufacturers and distributors. This is a client-facing role that requires both hunting and farming capabilities in a full 360° sales cycle.Key Responsibilities:Develop and maintain relationships with clients in the packaging and bottling industry.Identify and target new business through cold calling, referrals, and site visits.Provide expert advice on glass packaging solutions and product customization.Prepare and present quotations and negotiate terms with customers.Coordinate with logistics and production teams to ensure timely order fulfilment.Track and report on pipeline activity using CRM systems.Meet or exceed sales KPIs and revenue goals consistently.Willingness to travel for marketing trips in and around Cape TownPreparing and submitting reports (using Excel) to the international office.Coordinating with the international team for sourcing and order fulfillment. Candidate Requirements:3–5 years of sales experience in one of the following industries: Beauty and cosmetics packaging industry, pharmaceutical packaging industry, food and beverages packaging industry, and glass manufacturers and distributors.Proven track record in full-cycle B2B sales and meeting targets.Strong understanding of packaging product features, benefits, and applications.Valid SA driver’s license and own reliable transport.SA Matric qualification or Grade 12 equivalent; further training in sales or logistics is a plus.Excellent interpersonal and communication skills.Remuneration & Benefits:Salary: Max R22,000 per month CTC based on experienceCommission: Paid upon completion of each saleCar & Fuel Allowance:
https://www.jobplacements.com/Jobs/S/Sales-Representstive-1194772-Job-Search-06-14-2025-02-00-16-AM.asp?sid=gumtree
10mo
Job 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
14d
Job Placements
14
R 2,700,000
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Looking for smarter warehousing solutions? This new development is a fantastic opportunity for industrial users looking for a bespoke, customised industrial facility suited to their specific operations and requirements. The design, layout and internal specifications will be tailored to meet the needs of the tenant. Ideal for logistics operators servicing fast-moving sectors such as retail, e-commerce, pharmaceuticals and automative, the development will offer all the modern features needed for smart warehousing and value-added services that meet the demands of modern day supply chains and will prepare businesses for future growth. There are three letting options within the development, namely: 1 Unit - Warehouse: +- 6500m², Office 500m²2 Units - Warehouse: +- 12 900m², Office 1000m²3 Units - Warehouse: +- 19 300m², Office 1500m²Atlantic Hills is an industrial estate that offers unparalleled logistical advantages across the Western Cape. Strategically situated at the intersection of the N7 and M12, Atlantic Hills provides extensive access to all major transport routes in Cape Town, ensuring seamless connectivity.With the harbour and Cape Town International Airport nearby, Atlantic Hills is the ideal destination for businesses specializing in logistics, distribution, warehousing and manufacturing.Atlantic Hills strategic locations: - Direct access to the N7 highway via the Potsdam interchange- M12 and M13 Arterials , servicing Durbanville, Plattekloof and the major N7 & N1 highways- Cape Town Harbour (20 Minutes away)- Cape Town International Airport (25km)Contact me today for to register your interest and discuss further!Rates And Taxes: 1Levies: 1Property Reference #: 2389040Agent Details:Nicholas WalkerSwindon Property Services80 Strand Street, 7th Floor, Cape Town, 8001
2mo
Swindon Property Services
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