1,408 Quality Director jobs in Kenya
Associate Director, Global Quality Assurance
Posted today
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Position Description
Job Title
: Associate Director, Global Quality Assuranc
eLocation
: Nairobi, Kenya, Cape Town, South Africa; Remote-South Africa, Remote-Uganda, Remote-Nigeria, New York, New York; US - Remote Considered; United Kingdom – Remote; OR Amsterdam, Netherland
sReporting to:
Senior Director, Clinical Quality Assuranc
**e
Position Summar**
y:Are you a Quality focused leader in clinical development, passionate about bringing forward public health solution
s?
IAVI is seeking an experienced and detail oriented Associate Director, Quality Assurance who will ensure compliance of clinical development operations to IAVI and industry standards. The Associate Director will facilitate the Clinical Development group's participation in the IAVI management system where appropriate processes, procedures, and controls are established to ensure clinical research is conducted according to IAVI and industry standar
**ds.
Key Responsibilit**
- ies:Support Project Teams with the development of management plans relevant to the specific project
- (s);Support and prepare Project Teams for regulatory inspections and external Sponsor aud
- its;Serves as the GCP point person for the IAVI electronic QMS, and Clinical Trial Systems, development and implementat
- ion;Develop and implement QMS compliance assessments for the GCP component of the
- QMS;Develop and implement an eTMF inspection readiness assessment plan for all IND stud
- ies;Participate in executing the audit plan as delega
- ted;Provide training to GCP Operations on best practices and trends as indica
- ted;Oversees implementation of GCP CAPAs and conduct the required effectiveness che
- cks;Perform other tasks as assigned by the mana
**ger.
Education and Work Experi**
- ence:Masters Degree or equivalent in Clinical Research and/or Public Health or related field is requ
- ired.Minimum 10 years of experience in clinical research is required of which at least 3 in Quality Assurance is requ
- ired.Certification as GCP Auditor and/or Post Graduate Qualification in Quality Management is highly prefe
**rred.
Qualifications and S**
- kills:Strong knowledge and understanding of industry standards and research operations as pertinent to vaccine development is req
- uired.Experience working with management systems is req
- uired.Experience working with electronic data and records in CFR21Part11 compliant environments is highly desi
- rable.Experience as auditor of public health trials is highly desi
- rable.Experience working in remote-, virtual-, global-, teams, is highly desi
- rable.Ability to travel to research sites throughout the Africa region at up t
**o 30%.
Organizational Ov**
erview:IAVI is a nonprofit scientific research organization dedicated to addressing urgent, unmet global health challenges including HIV and tuberculosis. Our mission is to translate scientific discoveries into affordable, globally accessible public health solutions. Through scientific and clinical research in Africa, India, Europe, and the U.S., IAVI is pioneering the development of biomedical innovations designed for broad global access. We develop vaccines and antibodies in and for the developing world and seek to accelerate their introduction in low-income countries. IAVI programs and partnerships are grounded in the regions of the world where the disease burden is the greatest, and our approach emphasizes sustainability. Our network of clinical research center partners in Africa and India helps strengthen in-country research capacity and supports the training and education of the next generation of scientists. The global impact of our science includes fundamental contributions to understanding the biology of HIV infection, which IAVI and others are applying toward advancing vaccine science and immunology. IAVI accelerates scientific discovery and development by fostering unique collaborations among academia, industry, local communities, governments, and funders to explore new and better ways to address public health threats that disproportionately affect people living in poverty. Our global reach, including a clinical research network in five countries in sub-Saharan Africa and in India, has allowed us to make fundamental contributions to understanding the epidemiology, transmission, virology, and immunology of HIV. This work played a key role in facilitating the design of promising HIV vaccine candidates, as well as the discovery of broadly neutralizing antibodies that are now being advanced as promising approaches for HIV prevention. Our integrated capabilities in vaccine and antibody discovery, development, and clinical research take advantage of bio-pharmaceutical industry expertise to accelerate the development and testing of prevention methods for HIV and other diseases. Through the Product Development Center, we support external researchers with technical and scientific expertise to accelerate the development of their own pr
**oducts.
IAVI CORE**
- VALUES:Dedication to the Mission: We are committed to the translation of scientific discoveries into affordable, globally accessible public health so
- lutions.Innovative Evolution: We are committed to solving complex problems in creative and innovative ways, learning from our mistakes and successes and never g
- iving upIntegrity: We are committed to meeting the highest ethical and professional standards in everything we do and to taking responsibility for our actions to earn
- respectCollaboration: We are committed to embracing diversity, the power of global teamwork and the belief that by working as one we can make a di
fference
Disclaimer: Nothing in this job description restricts management's right to assign or reassign duties and responsibilities to this job at any time. The above statements are intended to describe the general nature and level of work being performed by individuals assigned to this position. They are not intended to be an exhaustive list of all duties, responsibilities and skills required of personnel so classified. This document does not create an employment contract, implied or otherwise, other than an "at-will" relationship. IAVI is an equal opportunity employer and applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disabilit
y status.
IAVI IS AN EQUAL OPPORTUNITY EMPLOYER dedicated to fostering a diverse and inclusive global organization. We recognize that a variety of backgrounds and perspectives enriches our work and strengthens our ability to achieve our mission. IAVI is committed to recruiting, developing, and retaining individuals through a merit-based approach. At IAVI, we celebrate the spectrum of colleagues' experiences and believe that dedication to our mission above all is essential to our success as a scientific non-profit organization focused on glob
al health.
Zer
o Tolerance
IAVI is an equal opportunity employer. It is IAVI's policy to provide equal opportunity without regard to race, citizenship, color, sex, gender identity or expression, age, height, weight, disability (including physical and mental conditions unrelated to job performance), religion, creed, caste, home language, ancestry, national origin, pregnancy, marital or partnership status, sexual orientation, status as a protected veteran, ethnicity, genetic information, predisposing genetic characteristic, status as a victim of domestic violence, stalking and sex offenses, HIV status, or any other status protected by applicable federal, state, or
**local laws.
Compensation And Benefit**
s Information:Salary is paid in local currency, and is commensurate and competitive with the loca
l labor marketPlease note, there may be some variation based on experience level. In addition, this position offers competitive benefits such as annual bonus, generous retirement savings plan, competitive health insurance benefits, and o
ther benefits.
Quality Control Inspector
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Company Description
At QIMA, we're on a mission to help our clients make products consumers can trust.
Working with over 30,000 global brands, retailers, manufacturers and food growers, we are on the ground wherever products are made. We help businesses secure every step of their supply chain with quality inspections, supplier audits, certifications, and lab testing, all powered by our intelligent digital platform.
Our team of 5,000 QIMers (and counting) across 40 offices and laboratories, are united in our shared passion for innovation and integrity, and guided by our QIMA values in the decisions we make every day. We believe in the work we do, and in making a positive difference in the world. Does this sound like something you'd like to be a part of?
Our Consumer Goods Division is dedicated to helping brands, retailers and manufacturers worldwide deliver safe, quality and ethically made products to their consumers. Every day at work, our inspectors, auditors, and lab techs use their expertise to help safeguard the products you use every day in your home: from clothes and footwear to toys and baby products, to electronics, appliances, and furniture.
Job Description
As a Quality Control Inspector, you'll be reporting to an Operations Manager and working as a part of our Operations team. At QIMA, the role of Operations is to deliver our industry-leading services to our clients while ensuring that all the work is performed to the QIMA standard of quality. Your role in this will be to:
- Check email daily in order to receive inspection documents and guidelines;
- Attend inspections on time and communicate with supplier in a professional way;
- Perform the inspection of the merchandise according with company procedures. Supervise the stuffing of the containers according with company procedures;
- Fulfill inspection reports according with company procedures and time lines.
Qualifications
Think you have what it takes? First of all, we want someone with:
- Experience in quality management, especially softlines/ garments/ textiles/ footwear (2 years or more);
- Knowledge of AQL standards, as well as relevant safety and quality regulations;
- Good command of English (spoken and written);
- Great attention to detail and strong professional ethics.
Additional Information
Does this describe you? Then we want to hear from you as soon as possible Apply now with your
CV in English
and we can write the next chapter of the QIMA story together
Quality Control Analyst
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Company Description
Accurate Steel Mills Limited, a leader in steel manufacturing, produces a range of steel products for the construction and fabrication industries. Our commitment to excellence over the past decade has distinguished our products in the market and fostered long-lasting customer relationships. With a vision to become East Africa's most reliable and trusted steel manufacturer, we provide superior quality steel products. Our mission is to drive economic growth safely across Africa by offering consistently dependable products that meet rigorous mechanical and chemical testing standards.
Role Description
This is a full-time on-site role for a Quality Control Analyst located in Nairobi County, Kenya. The Quality Control Analyst will be responsible for conducting quality control tests, ensuring products meet standards, handling laboratory equipment, and maintaining quality assurance protocols. The analyst will perform daily inspections, analyze data, and prepare reports to ensure that the highest quality standards are met throughout the production process.
Qualifications
- Strong Analytical Skills
- Experience in Quality Control and Quality Assurance
- Proficiency in Laboratory Skills and handling Laboratory Equipment
- Attention to detail and a methodical approach to work
- Understanding of safety protocols and regulatory standards
- Excellent communication and documentation skills
- Bachelor's degree in Chemistry, Engineering, or related field
- Previous experience in steel manufacturing or related industry is a plus
Quality Control Manager
Posted 4 days ago
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Key Responsibilities:
- Develop and implement quality control policies and procedures.
- Oversee all inspection and testing activities throughout the production process.
- Analyze quality data and identify trends or deviations.
- Implement corrective and preventive actions (CAPA) to address quality issues.
- Manage and train the quality control team.
- Ensure compliance with industry standards and regulatory requirements (e.g., ISO 9001).
- Conduct internal audits and participate in external audits.
- Collaborate with other departments to improve product quality.
- Maintain accurate quality records and documentation.
- Drive continuous improvement initiatives in quality management.
- Bachelor's degree in Engineering, Manufacturing Technology, or a related field.
- Minimum of 5 years of experience in quality control or quality assurance in a manufacturing environment.
- Proven experience in implementing and managing Quality Management Systems (QMS).
- Strong knowledge of statistical process control (SPC) and quality tools.
- Experience with ISO 9001 or other relevant quality certifications.
- Excellent leadership, communication, and problem-solving skills.
- Proficiency in quality management software.
- Ability to analyze data and generate actionable insights.
- Detail-oriented with a commitment to accuracy.
Quality Control Supervisor
Posted 6 days ago
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Key responsibilities include developing, implementing, and maintaining quality control systems and procedures. You will supervise and train QC inspectors, ensuring adherence to established protocols and standards. This involves conducting regular inspections of raw materials, in-process goods, and finished products, utilizing various measurement and testing equipment. You will analyze quality data, identify root causes of defects, and implement corrective and preventive actions (CAPA) to reduce waste and improve product consistency. Collaboration with production, engineering, and procurement teams is vital to address quality issues proactively. You will be responsible for managing quality documentation, including inspection reports, test results, and calibration records. This role also involves interfacing with customers on quality-related matters and ensuring compliance with relevant industry standards and certifications.
The ideal candidate will possess a Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or a Bachelor's degree in Quality Management. A minimum of 5 years of experience in quality control or quality assurance within a manufacturing environment is required. Prior supervisory experience is highly preferred. Proficiency with quality control tools and techniques (e.g., statistical process control, FMEA, Six Sigma) is essential. Strong analytical, problem-solving, and decision-making skills are critical. Excellent leadership, communication, and interpersonal skills are necessary to effectively manage a team and collaborate with other departments. Knowledge of ISO 9001 or other relevant quality management systems is a significant advantage. The ability to work effectively both independently and as part of a team is crucial. This hybrid role offers a balance between flexibility and hands-on involvement in ensuring product excellence.
Quality Control Chemist
Posted 15 days ago
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Quality Control Manager
Posted 15 days ago
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