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We are looking to recruit a permanent Responsible Pharmacist and the role will be based at the Cape Town Branch and will report to the Quality and Compliance Executive to ensure compliance with the medicines and related substances Act, Act 101 of 1965 and subsequently amended and the Pharmacy Act, Act 53 of 1974 and as subsequently amended.
Requirements:
B. Pharm. DegreeMin 3 Years’ experience in the Wholesale/ Distribution or Pharmaceutical manufacturing industry.Knowledge of GWP/GDP/GMPPharmaceutical Industry Laws and Regulations and Ethics.Current valid registration in good standing with SAPCStaff managementWriting skillExcellent computer skillsKnowledge of ISO standardsLegal Compliance
Duties:
To ensure compliance with Quality & regulatory standards and guidelines.To ensure that all licenses in respect of regulations are maintained for the branch.To maintain the Quality Management System (QMS) by preparing and updating SOP’s, conducting internal and external audits and monitoring staff training.To ensure effective management of product returns, product recall, destruction process and reporting of product complaints/ Adverse eventsTo ensure effective management of CAPAs & deviations and change controls calibration & maintenance of critical equipment.To ensure that product release and sampling are conducted within SLATo ensure that favorable audit reports are received from Distribution principals, to formulate replies to audits reports.To ensure management of the schedule 5 and 6 productsTo ensure that the validation plan is implemented and maintained.To ensure the availability of emergency after hours service.To ensure that there is continuous Pharmacist supervision of premises during operating hours.Responsible for all communication with SAHPRA and SAPC.
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Our client based in Coega, Port Elizabeth, is looking for an experienced Food Safety and Quality Compliance Officer; preferable with fruit industry experience.
EDUCATION AND EXPERIENCE REQUIRED:
Grade 12;Tertiary qualification (advantageous);3 years minimum experienceFruit industry knowledgeExposure to and understanding of implementation of OHSAS, food safety, HACCP and Siza, globalgap
PURPOSE OF THE POSITION:
Coordinate and monitor the implementation of the Companys Health and Safety policy.To ensure that the Company and its Contractors comply with the requirements of legislation by monitoring contractor compliance, attend and report at safety meetings and ensure statutory and regulatory compliance.To ensure that all products meet the standards set by both the company and regulatory authorities. They may develop and review quality and safety policies and manage audits by third-party inspectors.
KEY RESULT AREAS:
Analyse quality control reports from the receivers and feedback to growers.Maintenance of food safety accreditation: BRC and SizaRetention sample information is collected and analysedMaintain timely and professional communication with management, employees, and customers;Ensure that Quality Assurance procedures are strictly adhered to;Investigating and setting standards for quality and health and safety;Conduct Incoming shipment/delivery quality inspections on all produce linesPass on the information from the upper management to the employees and vice versa;Determining, negotiating and agreeing on in-house quality procedures, standards and specifications.Acting as a catalyst for change and improvement in performance and quality.Complete paperwork efficiently; andAd hoc duties and responsibilities assigned by Senior Management.
Please consider your application unsuccessful if you have not heard back from us within 2 weeks.
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Our manufacturing client, in the automotive sector, is seeking to appoint an experienced Assistant Metrologist in their Quality Department.
Minimum 5 years work experience in a factory / manufacturing environment secures.
This role is based out of in Port Elizabeth.
QUALIFICATIONS:
A tertiary qualification, e.g. BTech Quality, is preferredMinimum Matric with Math’s and ScienceQuality specific training in VDA6.3, ISO9001, IATF16949
KEY PERFORMANCE AREAS:
Measuring Programs development for measurement of new and existing wheelsProvide effective feedback to all relevant departments if dimensional deviation or defects identifiedPrepare PPAP/ISIR documentation according to Customer requirementsParticipate in FMEA-Meetings and Control Plan-Meetings (Part of APQP)Support with conduct of Routine testing and Product auditsCalibration – Maintain calibration status of all existing gauges and instruments – inclusive of physical verification of instruments in accordance with works instructions, as well as all relevant documentation. Manage external calibration processes.Capability studies/ad-hoc measurements as part of investigations; assist with investigations into wheels not meeting requirementsDocumentation and record – Maintain relevant filing systems (including drawings and measuring reports, registers and issue levels).
WORK EXPERIENCE:
Minimum 5 years work experience in a factory environmentShould have thorough knowledge of the entire plant processesThorough knowledge of Quality StandardsShould have experience with SPC/MSA/APQP/8D concepts
OTHER REQUIREMENTS:
Understanding of CMM Measuring equipmentThorough knowledge of Sampling processAbility to interpret drawingsAbility to work under pressure, be a team playerAbility to be pro-active, good time management skillsHonest, have integrity and good communication skillsExcellent attendance recordComputer literacy is essential (Excel, Word, PowerPoint, AutoCAD, MiniTab)Must have a valid Drivers License (own transport preferable)
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Our client in the Marketing Industry based in Port Elizabeth is currently looking to employ a Data Scientist.
An awesome career opportunity awaits.
Requirements:
3 - 5 years minimum experience in a research environment.Honours Degree level qualification – Statistics/Mathematics/Engineering.Meticulous attention to detail.Ability to work under pressure.Ability to prioritise and multitask.Team player.Self-disciplined.Deadline driven.Excel proficiency a must.Experience with programming languages.SQL, SAS, SPSS, Power BI proficiency advantageous.
Responsibilities:
Designing of adequate samples, surveys, methodologies and universe structures for new project during project setup phase.Evaluate universe and sample designs for existing projects and implement changes where necessary.Assist with complex data investigations and analysis within the department.Consultations with relevant departments to solve data-related challenges.Provide guidance to the correct use of reported data.Set up and review data verification methods to optimize processes.Assist with designing more efficient production processes.Manage and implement data restatements for relevant projects.Assist with building data models, data visuals as well as complex calculations using tools provided.Any other related tasks that may arise from time to time.Monitor and follow up on timelines for assigned projects.Assist with project setups where applicable.Receive and delegate project specific requests from internal departments.Data review and sign off.Report generation and updates.
Please note should you not receive a response within two weeks of applying please consider your application unsuccessful.
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DATA CAPTURER Eastern Cape SGS is the worlds leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 89,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world.SGS South Africa is seeking to fulfil a key role in the SGS Matrolabs Eastern Cape Civil Engineering Laboratories. The role includes but are not limited to assisting the Supervisor/ Laboratory Manager, perform administrative duties to provide assistance to SGS- Matrolab Laboratory and/or site laboratory especially with the capturing of data. The ideal candidate for this position will be a person with strong and assertive leadership skills to command respect from those he/she deals with, whilst possessing enough energy and passion to maintain good staff relationships. A successful career in delivering performance against agreed strategic objectives and ultimately ensuring that all quality and testing methods are observed, and any deviation is reported without delay. Primary Job Responsibilities Reporting to the Laboratory Supervisor / Laboratory Manager, you in the role, are expected to: General Processing of Data accuratelyMeeting deadlinesEnsure adherence to Standard Operating procedures Accurate capturing of data in an efficient time frame Ensure adherence to company Code of Ethics Ensure adherence to Quality Management Systems & implementation of Quality System Ensure all duties are performed in accordance with accepted service delivery standards Maintain quality, efficiency and confidentiality of service Liaise with and assist Supervisor / Manager Adhere to all quality and safety requirements of the SGS management system Perform any other reasonable tasks as assigned by direct line manager Administration (any of the following as assigned and trained Ensure all messages are conveyed to relevant people Assist with the maintenance of the sample registration as and when requested Complete all work in an efficient manner and without delay Sample handling and distribution of results (any of the following as assigned and trained Ensure prompt and efficient handling of documents and other instructions as trained and per applicable procedure Attend to operational matters related to new and repetitive instructions received from supervisor/manager Typing of documents including but is not limited to reports, e-mails and documents Adhere to all quality and safety requirements of the SGS management system Perform any other reasonable tasks as assigned by direct line manager Qualification and Experience Education : Grade 12 Must be proficient in English (Read,Write, Speak)Computer Literacy Word, Excel, OutlookAdministrative experience will be an advantage. Remuneratio
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*Reference: DUR002352-SN-1*
Our client is seeking a qualified and experienced individual to join their Management team in setting Operative Manufacturing Standards for their Business Units. Reporting to the General Manager, ensure an efficient, productive process and facilitate a world-class manufacturing environment, achieving safety, quality and productivity targets.
*Minimum **Requirements:*
* A Degree or Diploma in Engineering or related field.
* Minimum 10 years’ experience in a similar role.
*Key Performance Areas:
*
Health & Safety Management:
* Identify potential hazards and critical safety issues in all plants.
* Promote a culture of safety first and a working environment that protects the health of all employees.
Quality Management:
* Comply with requirements of the manufacturing quality management systems.
* Promote a culture of quality excellence.
Financial Management and Cost Control:
* Provide input into the budget process.
* Monitor performance against budget (expense controls, variances, etc.).
* Protect company assets (working capital & fixed assets).
* Detect and prevent fraud.
* Promote good corporate governance.
* Participate in the audit process.
Plants:
* Provide coaching and mentoring to ensure standard cycle times are maintained and improved for all production processes.
* Provide support for the plants at internal sample and production trials.
* Ensure the execution of change requests in the plant are actioned and monitored.
* Support problem solving on the process and equipment to rectify issues or improve the process.
* Promote good housekeeping and safety.
Projects:
* Support and mentor the development of production processes for client and internal projects.
* Assist in the definition or planning of new equipment for incoming projects.
* Investigate new technologies relevant to the production processes within the plant.
* Prepare and present technical reports and presentations to management.
* Support and advise with current and future plant layouts.
Continuous Improvement:
* Champion the Continuous Improvement Program team within the Business Unit.
* Ensure projects are monitored against deliverables.
* Provide monthly report of achieved progress vs. target.
* Keep up to date with latest trends and developments through technical literature and technical seminars or trade fairs.
* Benchmark manufacturing processes and technology against best practices.
* Continually measure, monitor and provide improvement plans for improving business systems efficiency and cost reduction programs.
* Recommend establishment of technical alliances where considered beneficial.
Maintenance:
* Implement planned maintenance.
R
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Location: Port ElizabethSalary: R36 000 to R43 000 per month commensurate with experience and qualification Qualifications / Requirements:• Minimum of Diploma in Purchasing Management or equivalent• Minimum of 5 years’ experience with relevant purchasing knowledge of raw materials and complex specifications• MRP/ERP system experience related to purchasing and BOM’s• A track record of cost saving initiatives• Be prepared to complete an assessment and interview processKey Performance Areas:• Responsible for the purchasing various goods including machinery, equipment, raw materials and/or other supplies for internal consumption• Reviewing purchase orders, conferring with other departments to verify orders, contacting vendors and evaluating bids/quotations offered by suppliers• Assisting with the development and implementation of various purchasing procedures, inventories, accounts, proposals and similar preparations• Process special orders for customers• Request inventory counts and/or stock checks where appropriate• Obtaining and negotiating prices, delivery, terms and sources of supply in accordance with specified policies and procedures• Ensure and maintains daily outputs• Communicate effectively with other workers to direct personal workflow• Verify charges indicated on purchase orders and requisitions against cost centre accounts• Evaluate and review bids/quotations submitted by suppliers• Monitor supplier performance with regards delivery, quality and quantity• Assist in the identification and establishment of sources of supply and the inspection of samples• Expedite goods by contacting vendors regarding shortages and administering overcharges and breakage, etc• Investigate information pertaining to the preparation of proposals and specifications• Develop and maintain files of reference materials such as supply catalogues and brochures• Use computer applications or other automated systems such as spreadsheets, word-processing, calendar, e-mail and database software in performing work assignments and provide reports• Perform any other incidental tasks, as needed
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Responsibilities: Deliver a variety of spa services in a safe and comfortable manner.Maintain equipment and sample inventory of products.Keep documentation and maintain clients’ files.Keep a clean and stocked room.Acknowledge and respond to relevant customer queries, needs and expectations.Suggest and promote retail products or additional services.Follow health and safety regulations.Uphold hygiene standards.Report any issues to administration.Apply best practices and be up to date with market trends.Requirements: At least 2 years’ experience.Valid Driver’s License.Must be able to communicate in English with excellence.Must be Qualified in Microblading and Waxing - Not negotiable. Strong Customer service skills.Sales knowledge and focus.Must work well under pressure, while maintaining high standard service.Well groomed.Reliable transport.Must be able to work shifts.Must have a positive attitude and an uplifting personality.Must work well in a team.Please consider your application unsuccessful should you not receive a response within two weeks of applying.
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Applications are invited from suitably qualified & experienced employees to fill the above vacancy in Production – Final Assembly Job Description and ResponsibilitiesFor Bolting related changes (new model introduction, PDM Changes, etc.), update TORIS Matrices (Torque parameters per fastening of bolts) and ensure TORIS daily sample adherence to Group Standard. Liaise with relevant stakeholders to ensure that Process documentation such as Control Plans, MAC and SOS Sheets are maintained/updated regularly and that the Bolting problems are sufficiently addressed.Continuously monitor, update and calibrate Electronic Torque Transducers and DataMyte to ensure conformance to quality standards. Ensure proper protection of equipment to avoid damages and scratches.For proper analysis and feedback on TORIS Inspection data, ensure consistent downloading of Torque data from DataMyte onto computer through SPC Management software.Perform Annual review of TORIS Torque Verification Specifications to ensure the set-up specification stays relevant.For samples found to be out of specification, ensure that the necessary verification processes are followed by TORIS Inspectors that Production is informed of non-conformance and that actions are taken to address the risk. Where A & B Category Bolts are not performed with Smart Tools, ensure that the necessary controls are put in place to ensure adherence to Quality Requirements.Coordinate Bolting parameter changes on Torque Controllers in Final Assembly, document changes according to appropriate Quality Managements System requirements and ensure communication to all relevant stakeholders.Update Bolting Work Instructions, review FIS-eQS Bolting descriptions and Bolting Reports.Ensure continuous improvement of Bolting Processes, compliance to VW Bolting Standards and adherence to Bolting KPI’s. Form part of team for Audit Preparations; accompany auditors when requested and action Bolting relating findingsEducation and ExperienceA National Diploma/ Degree in Mechanical / MechatronicsMinimum 5 years’ experience in manufacturing industry.Experience in a maintenance / production environment.Skills, Attributes & Other requirementsESSENTIAL:Be proficient in MS Office, specifically MS Excel.Have a sound knowledge of SQL, with the ability to construct and write queries against various databases.Have a strong analytical and problem solving abilityHave knowledge of the companies processes, of Material properties, Tensile Strength and Hardness that can affect Bolting applications.Have good communication, presentation skills and be a strong team player.PREFERRED:Basic knowledge of the DAR system would be an advantage.Basic knowledge of the German language would be an added advantage Please forward CV and ALL supporting documentation to, recruiter@profilepersonnel.co.za. Should you not hear from Profile Personnel within 14 days please consider your application unsuccessful for the vacancy. Please note all applications will automaticall
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At Lancet Laboratories we recognise that results are achieved through attracting, developing and retaining the best people. We support the attainment of equal opportunity progress, and believe that people are the spirit to us accomplishing our strategic goals.
An opportunity has presented itself to appoint a suitably qualified candidate into the position of* Medical Technologist (Micro)*. These positions are based at *Lancet Laboratories *in *East London* and will be reporting into the *Laboratory Manager*.
*POSITION SUMMARY: *Performs and analyses laboratory samples in order to provide results for medical practitioners to diagnose, treat and prevent diseases.
• Performs diagnostic testing procedures, reviews and verifies results and interacts with pathologists on technical matters to provide all relevant data that may pertain to the prevention, diagnosis or treatment of diseases.
• Operates, maintains and calibrates the equipment used in the laboratory to ensure that it is operating efficiently and providing accurate results. This includes recording instrument maintenance and quality control results as well as recognising and resolving problems by troubleshooting mal-functioning equipment and taking corrective action.
• Implements sound housekeeping procedures and work effectively with others as a member of a team to ensure a safe working environment in accordance with safety protocols. This includes the on-going maintenance of quality control standards, adherence to infection control measures, correct disposal of bio-hazardous waste and participation (as per delegated responsibilities) in the preparation process for internal and external audits.
• Assists the laboratory manager with overseeing and monitoring equipment maintenance, asset management, procurement of goods and staff overtime expenditure to ensure the most effective utilisation of resources, optimisation of stock levels and reduction of costs at all times
• Reports incidents, including instrument failures, problem solutions and reads documents and actions tasks on the laboratory information management system in compliance with relevant organisational policy.
• Attends training and seminars and participates in continuing professional development (CPD) activities to continuously update knowledge and skills as well as comply with professional registration requirements. This includes ensuring the availability of up to date records that can be presented immediately on request thereof.
• Performs on-site training of laboratory staff, interns, students, medical colleagues and associated health workers in laboratory techniques, processes and systems, if assigned by laboratory manager and deemed competent.
• Adheres to professional conduct requirements in line with organisational policy and relevant professional body ethical standards.
• Represents the organisation by applying the principles of customer care in the medical pathology field and interacts profession
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Overseeing daily business activities, improving overall business functions, training staff, managing budgets, developing strategic plans for improving customer service, creating policies and communicating business goals. Support to the directors, Area Managers, Sales team and staff Continuous training on SAP, Operations, Health and Safety RESPONSIBILITIES Ensure policies and procedures are kept up to date and followed Ensure monthly tasks of the warehouse team are being tended to Review weekly stats reports for team and assess productivity in weekly meetings with team leader and feedback for the directors Review weekly credit note stats Handle all warehouse queries – high level Apply sales strategy set out by the MD Liaise with reps and customers on specific stats requirements relating to queries Liaise with Operations Director on reporting before communications are sent out to ensure data is accurate and relevant Understand reporting and liaise with Directors on ways to make improvements and possible steps to implement as cautionary measures Tracking of monthly Sales, Turnover Building required reports for the directors Set up sales meetings and agendas as necessary Manage Inactive Sampling by checking reports monthly and liaising with Sales & Marketing Director and Area Managers for solutions Responsible for all daily operations Learn inbound and outbound shipments when required Ensure health and safety standards are meet Learn to scrap and un-scrap stock in the warehouse Oversee the warehouse movements from SAP Ongoing training for all departments Backup to group operations director MINIMUM EDUCATION & EXPERIENCE Diploma in office management Minimum 5 years’ experience in similar role SAP S/4 HANA MS Office Intermediate level Strong Excel Skills Strong organizational skills Must be able to handle staff requirements Excellent time management skills Health and Safety Good understanding of daily business operations KEY COMPETENCIES REQUIRED High Customer ethic Demonstration of a good understanding of and commitment to Company goals and values Strong interpersonal skills Exceptional communication skills – verbal and written – with strong focus on attention to detail Exceptional time management skills with strong ability to be detail and results driven Team player with ability to motivate and lead others Thorough understanding of business principles and practices Organizational & planning skills Critical thinking & problem-solving skills Researching & investigative nature Leadership skills
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Overview
Leads supplier development, supplier negotiations, RFQs, and CMO category strategy for major suppliers. Identifies continuous improvement opportunities.
Responsibilities
Supplier management
Communicate and negotiate with suppliers
Monitor quality standards and identify performance failures
Report on supplier performance
Manage supplier communications and documents and process flow, including RFIs, RFP, RFQ, and RFB’s
Resolve supplier issues; maintain working relationships with key suppliers
Set up new vendors and coordinate with legal to support new contracts; maintain/ update existing contracts
Identify new suppliers in the marketplace
Vet potential suppliers’ capabilities (delivery, quality, services)
Review insourcing and outsourcing opportunities
Negotiate with suppliers to carry stock for fast moving items
Provide advice and guidance to customers on procurement processes
Review and approve price variances (Order vs Invoice Prices)
BBBEE and procurement administration when required
Risk management
Maintain and report on adherence to internal and external compliance requirements
Actively reduce third-party risk exposure
Carry out risk management processes within CMO category
Quality and qualifying products
Assist quality teams to obtain products needed to conduct finished product testing
In conjunction with Technical Project Manager, schedule product trials and coordinate samples
Reporting and record keeping
Maintain repository of procurement-related knowledge
Maintain complete, compliant documentation of purchasing activities
Maintain standards and update SOPs for documentation and filing requirements
Budgeting
Manage and optimise use of Category budget
Provide input into required changes in resources to enable achievement of objectives
Monitor, track and report on expenditure against budget
Planning and coordination
Optimise processes, identify gaps in policies, procedures and legislation, and propose changes or improvements to management
Provide technical advice to internal stakeholders
Job Requirements
Background/experience
6 years relevant experience
Experience in a manufacturing procurement environment, and preferably with significant experience in a CMO environment
Minimum of a National Diploma in relevant field (Procurement, Supply Chain Management, Finance/Commercial), or a related discipline
Specific job skills
Computer literacy
Competencies
Customer Awareness
Meeting Deadlines
Making Decisions
Planning and Organising
Interrogating Information
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At Lancet Laboratories we recognise that results are achieved through attracting, developing and retaining the best people. We support the attainment of equal opportunity progress, and believe that people are the spirit to us accomplishing our strategic goals.
An opportunity has presented itself to appoint suitably qualified candidates into the day shift positions of* Medical Technologist (Clinpath)*. These positions are based at *Lancet Laboratories *in *East London* and will be reporting into the *Laboratory Manager*.
*POSITION SUMMARY: *Performs and analyses laboratory samples in order to provide results for medical practitioners to diagnose, treat and prevent diseases.
• Performs diagnostic testing procedures, reviews and verifies results and interacts with pathologists on technical matters to provide all relevant data that may pertain to the prevention, diagnosis or treatment of diseases.
• Operates, maintains and calibrates the equipment used in the laboratory to ensure that it is operating efficiently and providing accurate results. This includes recording instrument maintenance and quality control results as well as recognising and resolving problems by troubleshooting mal-functioning equipment and taking corrective action.
• Implements sound housekeeping procedures and work effectively with others as a member of a team to ensure a safe working environment in accordance with safety protocols. This includes the on-going maintenance of quality control standards, adherence to infection control measures, correct disposal of bio-hazardous waste and participation (as per delegated responsibilities) in the preparation process for internal and external audits.
• Assists the laboratory manager with overseeing and monitoring equipment maintenance, asset management, procurement of goods and staff overtime expenditure to ensure the most effective utilisation of resources, optimisation of stock levels and reduction of costs at all times
• Reports incidents, including instrument failures, problem solutions and reads documents and actions tasks on the laboratory information management system in compliance with relevant organisational policy.
• Attends training and seminars and participates in continuing professional development (CPD) activities to continuously update knowledge and skills as well as comply with professional registration requirements. This includes ensuring the availability of up to date records that can be presented immediately on request thereof.
• Performs on-site training of laboratory staff, interns, students, medical colleagues and associated health workers in laboratory techniques, processes and systems, if assigned by laboratory manager and deemed competent.
• Adheres to professional conduct requirements in line with organisational policy and relevant professional body ethical standards.
• Represents the organisation by applying the principles of customer care in the medical pathology field and interac
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Our client based in Middelburg (Mpumalanga) is looking for an experienced Spectrochem Laboratory Chemist. Person Specification: Must be pro-active, innovative and demonstrate high levels of flexibility.Must be able to work under pressure.Must be able to work without direct supervision, be a self-starter and use own initiative to make decisions.Excellent planning and organizing skills are essential.Hold a B.Sc. degree in Chemistry or equivalent qualification.5 – 8 years’ experienceExcellent planning and organizing skills are essential.Experience with XRF (3 - 5 years of experience), OES, LECO and/or sample preparation will be highly advantageous.Must be willing to work standby and overtimeJOB RESPONSIBILITIES Development and validation of new and existing analytical methods.Optimisation of current methods.Calibration of XRF, OES and LECO instrumentation.Analyses of non-routine sample to ensure accurate results are reported.Ensure all equipment requiring external calibration is calibrated and fit for purposeTrouble shooting and problem solving.Development and maintenance of quality assurance system.Commissioning of new equipment.Please consider your application unsuccessful if you have not heard back from us within 2 weeks.
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GRAPHIC DESIGNER BASED PORT ELIZABETH Our client a leading Technology and Media Company, requires the services of an experienced Graphic Designer to join their young and dynamic team. Key Performance Areas (Any experience in below KPA will be advantageous) Experience as a Graphic Designer within a Marketing Agency, servicing multiple Companies across multiple Business Sectors.Ability to create sample designs that meet client requirements, derived from project briefs.Prepare digital artwork suitable for proofing and/or printing across various applications.Prepare preliminary & final proofs and check for errors and amend where necessary.Create & apply our Clients’ Corporate Identity to all their Marketing Material (Digital & Print).Work with the Media Team, Clients and Management to see projects through to completion, by planning, multi-tasking and prioritising effectively.Ability to Copyright content for all our Clients’ Marketing Material, including but not limited to, Websites, Brochures, Adverts etc. Personal Attributes Must be able to work under pressure.Must be able to work on multiple projects simultaneously and prioritize accordingly.Must be Self-Motivated and able to work under general supervision, with close attention to detail.Must be a good Team Player as the nature of the role requires comfortable interaction and liaison with Management, Co-Workers and Clients.Raw design talent must be evident.Must have strong conceptual skills.Must have strong production skills in order to provide solutions, within the constraints of both the Print & Digital space.Ability to produce accurate results within prescribed deadlines.Neatness & attention to details in work is essential.Passion for the IT & Media/Marketing Industry.Results driven, positive and professional disposition.Client service skills and customer approach.Excellent Interpersonal; verbal and written communication skills.Excellent time management skills.Positive, confident approach to work and colleagues.Honest and reliable.Self-Motivated.Sober Habits.Driver’s license and own transport essential. Technical Knowledge and Skills Experience and Qualifications Minimum of 3 Years’ experience as a Graphic Designer/Creative Visualiser.A relevant Degree/Diploma in Graphic Design.Fully literate with the Adobe Creative Suite:o InDesign.o Photoshop.o Illustrator.o Lightroom.Fully literate with Coral Draw.Proficient with Microsoft Office Applications.All applications are to be accompanied by a Graphic Design Portfolio. Package Offered This position will attract a Market Related salary according to qualification and experience gained.
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA5XzUzMzc4X180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1126000&xid=1109_53378
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Our prestigious client based in Middelburg (Mpumalanga) is looking for an experienced Laboratory Chemist. Requirements: Hold a B.Sc. degree in Chemistry or preferably MSc Degree in Chemistry. 5 – 8 years’ experience.Must be pro-active, innovative and demonstrate high levels of flexibility.Must be able to work under pressure.Must be able to work without direct supervision, be a self-starter and use own initiative to make decisions.Excellent planning and organizing skills are essential.Excellent planning and organizing and administrative skills are essential.Experience with method development, calibration, optimization, validation and analytical problem solving on XRF, OES or ICP (minimum of 3 years of experience).XRF experience can be excused if they have method validation experience and method development especially on ICP on more than 1 type of material (not just water or coal for example).Must be willing to work standby and overtime. Job Responsibilities: Development and validation of new and existing analytical methods.Optimization of current methods.Calibration of XRF, OES and LECO instrumentation. Analyses of non-routine sample to ensure accurate results are reported.Ensure all equipment requiring external calibration is calibrated and fit for purposeTrouble shooting and problem solving.Development and maintenance of quality assurance system and administration thereof.Commissioning of new equipment.Develop methods with current equipment meeting the criteria, quality controls and to test correctly, also to maintain quality even on old equipment.This is a specialist role and not a management or team manager role. Please consider your application unsuccessful if you have not heard back from us within two weeks of applying.
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA5XzgyODkwX180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1211689&xid=1109_82890
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Minimum requirements: Excellent planning and organizing skills are essentialHold a B.Sc. degree in Chemistry or equivalent qualification5 8 years experienceExcellent planning and organizing skills are essentialExperience with XRF (3 - 5 years of experience), OES, LECO and/or sample preparation will be highly advantageousMust be willing to work standby and overtime Consultant: Anna-Belle Ehrke - Dante Personnel Mpumalanga
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA5Xzg4MjU5X180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1219780&xid=1109_88259
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RESEARCH NURSE 12 MONTHS FIXED-TERM CONTRACT EAST LONDON, EASTERN CAPE The Desmond Tutu Health Foundation (DTHF) is a registered non-profit organisation focused on the pursuit of excellence in research, treatment, training and prevention of HIV and related infections in Southern Africa. We have fantastic job opportunities across our businesses for talented people wanting to realize their full potential. Could that be you? If so, we invite you to explore the possibility of joining us to play your part in Desmond Tutu Health Foundation exciting future.We invite applicants to apply for this 12 months fixed- term contract post at the Desmond Tutu Health Foundation as part of a project encouraging ART initiation in young people in South Africa (primarily in the Duncan Village area in East London).Requirements: Nursing Degree or Diploma, with active registration with the South African Nursing Council (SANC) as a Registered NurseAt least 2 years nursing experience, with knowledge of HIV diagnosis and managementExperience working in Buffalo City Metro specifically, or Eastern Cape in generalFluent in isiXhosaAt least 1 year research experienceAt least 1 year staff management experienceExperience in PhlebotomyExperience of working with adolescent in the health sectorValid drivers licenceComputer literacy with sound knowledge of email, word processing and internetStrong verbal, written and interpersonal communication skillsAbility to work well under pressure and to maintain effectiveness during changing conditionsClient focusedExcellent Administration skillsMust be able to work as a member of a team and independentlyMust be detail orientatedWillingness to travel and work irregular hours, including weekends from time to timeAdvantageous: Good Clinical Practice (GCP) certificateKnowledge of Duncan Village and/or Scenery Park communitiesResponsibilities: Providing a client focused youth friendly sexual and reproductive health serviceMaintaining strict client confidentialityProviding post-test counselling, as well as education on ARV (antiretrovirals), STI (sexually transmitted infections), contraceptionObtaining blood and tissue samples and processing them as requiredCorresponding with the laboratory regarding query resolutionPerforming other client care procedures as requiredEnrolling eligible participants onto the study, includes performing Informed Consenting process according to GCP guidelinesEntering data on case report forms and processingPerforming Quality Control (QC) checks on CRFs (clinical research forms) and source documentsProviding feedback to project lead on recruitment and participants follow-up visitsManaging filing of CRFs (Clinical research forms), source documents and laboratory reportsOversee facilitator of the intervention sessionsReferral of clients to
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA5XzcxNzQzX180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1182499&xid=1109_71743
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PROJECT COMMERCIAL ADMINISTRATOR Eastern Cape SGS is the worlds leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 89,000 employees, SGS operates a network of over 2,600 offices and laboratories around the world.SGS Matrolab is seeking to fulfil a key role in the Eastern Cape Civil Engineering Laboratories. The role requires the incumbent to Perform business administrative duties to provide assistance to Industrial management, operations, technical staff and customers. The ideal candidate for this position will be a person that is disciplined and treat colleagues and management with respect, deadline & revenue driven and possessing enough energy and passion to maintain good staff relationships. A successful career in delivering performance against agreed strategic objectives and ultimately ensuring that all quality and testing methods are observed, and any deviation is reported without delay. Primary Job Responsibilities Reporting to the relevant Laboratory Manager and are expected to: General Perform any reasonable tasks as assigned by direct line manager.Administration CRS coordination - coordination of inspection and testing activities. Business Procurement AdministrationEnsure Preferred Suppliers are used Purchase Requests Receiving of services/goods Order follow up Supplier performance feedback Business Support Apply Procurement policies and procedure Petty Cash to be done inline with SGS procedures and submitted timeously. Liaison with customers via telephone or email. Ensure all messages are conveyed to relevant people. Adhoc administration duties required by the line manager. Travel arrangements for manager / Technicians etc. Filing and maintenance of filing system.Finance (If Required) Request new customer accounts be opened. Raise and follow-up on Purchase Orders. Arrange and follow-up payment for CBD or COD suppliers. Providing instructions to Finance for invoicing. Feeding information to Finance as and when required. Ensure accurate and timeous frontloading, if and when required. Process and submit claims as per company procedure within deadlines. Sample handling and distribution of results Ensure prompt and efficient handling of samples as trained and per applicable procedure. Attend to all operational matters related to work in progress at sample reception and new instructions received from customers / line Manager. Preparation of test reports, emailing of results to customers, manual and electronic filing of job and / or test report. Quality & Health & Safety System Adhere to all quality and safety requirements of the SGS management system. Actively participate in safety related activities. Always wear appropriate protect
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Main purpose of the job: To analyze, interpret and produce patient results on blood, body fluids (i.e. urine, CSF, and other fluids), and specimens and to implement and maintain the quality management system for the laboratoryLocation: Mthatha – Eastern Cape Key performance areas: Receive labeled and captured samples from Data CapturersCheck and verify if details on tubes and labels correspondCheck the suitability of samples to be analyzed i.e., no clots, not haemolysedCheck the tests required and log them on the worksheetPerform instrument and manual testsRead slides under microscope and comment (morphology)Analyze and interpret the results according to the study requirementRe-run tests as and when requiredFollow up on incomplete tests and ensure completion thereofCapture manual test results on laboratory information systemPrint the test results and correlate data with the systemInitial print out and file it according to SOPContact relevant Clinicians if abnormal and CSF results have been producedRecord feedback is given to relevant Clinicians/clientStore specimens in the fridge as per laboratory proceduresTroubleshooting and referring to Lab Coordinator or Laboratory Manager when necessaryProcessing of internal and external QCMaintenance and calibration of equipment, checking of freezer and fridge temperatures, liquid nitrogenDecontamination and maintenance of all equipment and work surfaces doneMonitor and control stock levels and advise if goods must be orderedMonitor and control workflows and turnaround timesPerform relevant administration i.e., filing, copying, faxing, etc.Report any quality control issues to laboratory managementPrint outstanding lists at the end of the shift to ensure that all tests have been performed and resulted – hand overRequired minimum education and training: National Diploma in Biomedical Technology Registration with Health Professions Council of South Africa as a Medical Technologist Required minimum work experience: Minimum 2 years experience in a clinical pathology laboratory Desirable additional education, work experience, and personal abilities: Certification in good clinical laboratory practice (GCLP) and basic health and safetyExceptional organizational and administration skillsKnowledgeable in Microsoft Office and laboratory systemsAbility to work under pressure and adhere to deadlinesWilling to work and be exposed to hazardous and infectious samplesAbility to work independently and as part of a multidisciplinary teamMust be willing to work shifts if required, and overtime may be required from time to timeMust be willing to work in a pressurized environment to meet turnaround times in high volumesTO APPLY: Only if you do meet the minimum job requirements and experience as mentioned above, you may submit a detailed updated CV.
https://protool.gumtree.co.za/external-link-browser.html?url=aHR0cHM6Ly9lbi16YS53aGF0am9icy5jb20vY29vcG9iX19jcGxfX18xMTA4XzcyOTQ3X180OTc/dXRtX3NvdXJjZT1ndW10cmVlJnV0bV9tZWRpdW09ZmVlZCZrZXl3b3JkPQ==&jid=1266710&xid=1108_72947
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