948 Industrial Engineering jobs in Kenya
Remote Senior Quality Assurance Engineer - Manufacturing
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Key Responsibilities:
- Develop, implement, and maintain robust quality assurance programs and procedures for manufacturing.
- Design and execute comprehensive test plans and protocols to ensure product quality and performance.
- Analyze production data and quality metrics to identify trends, root causes of defects, and areas for improvement.
- Conduct audits of manufacturing processes to ensure compliance with quality standards and regulations.
- Collaborate with engineering and production teams to resolve quality issues and implement corrective actions.
- Develop and deliver training programs on quality standards and best practices.
- Stay abreast of industry trends, new technologies, and regulatory changes impacting quality assurance.
- Champion a culture of quality throughout the organization.
- Manage documentation related to quality control, including SOPs and test reports.
- Contribute to product development by providing quality assurance input during the design phase.
Qualifications:
- Bachelor's degree in Engineering (Mechanical, Electrical, Industrial), Quality Management, or a related technical field.
- Minimum of 7 years of experience in Quality Assurance or Quality Control within a manufacturing environment.
- Strong knowledge of quality management systems (e.g., ISO 9001) and statistical process control (SPC).
- Experience with various testing methodologies and tools.
- Proficiency in data analysis and reporting.
- Excellent problem-solving and analytical skills.
- Strong understanding of manufacturing processes and product development lifecycles.
- Exceptional communication and collaboration skills, essential for remote teamwork.
- Ability to work independently, prioritize tasks, and manage projects effectively.
- Detail-oriented with a commitment to maintaining high-quality standards.
This fully remote opportunity offers the flexibility to work from anywhere while making a significant impact on the quality of our manufactured products. Join our innovative team and lead the charge in ensuring excellence.
Lead Industrial Process Engineer - Remote
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Lead Industrial Engineer - Remote
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Lead Industrial Process Engineer
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As the Lead Industrial Process Engineer, you will manage a team of engineers and technicians, providing technical guidance and mentorship. You will also collaborate closely with production, quality assurance, and R&D departments to troubleshoot complex issues, develop new manufacturing techniques, and integrate new technologies. Key responsibilities include conducting feasibility studies, developing process simulations, and preparing detailed engineering reports. You will also be involved in capital expenditure planning, equipment selection, and process automation projects. A strong understanding of statistical process control (SPC), Six Sigma methodologies, and project management is essential. This role offers a blend of on-site engagement for critical project work and operational oversight, with the flexibility of remote work for analytical tasks, reporting, and team coordination when appropriate.
The ideal candidate will possess a Bachelor's or Master's degree in Industrial Engineering, Mechanical Engineering, or a closely related field. A minimum of 8 years of relevant experience in industrial engineering, with at least 3 years in a leadership or supervisory role, is required. Demonstrated success in process improvement initiatives, cost reduction, and productivity enhancement is a must. Proficiency in process simulation software (e.g., Arena, FlexSim) and CAD software is highly valued. Excellent communication, interpersonal, and leadership skills are necessary to effectively manage teams and stakeholder relationships. We are looking for a proactive individual who can drive change and foster a culture of operational excellence. This is an exciting opportunity to make a significant impact on our client's manufacturing success.
Senior Industrial Automation Engineer
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Key responsibilities include developing technical specifications for automation projects, selecting appropriate hardware and software components, and programming PLCs (e.g., Siemens, Allen-Bradley) and robotic systems. You will conduct system integration, testing, and validation to ensure optimal performance and reliability. Troubleshooting and diagnosing issues with automated systems, both remotely and potentially through on-site visits when required, will be a significant part of your role. You will also play a key role in developing and implementing predictive maintenance strategies for automation equipment to minimize downtime. Collaboration with mechanical engineers, electrical engineers, and production teams to ensure seamless integration of automation solutions into existing manufacturing processes is essential.
The ideal candidate will possess a Bachelor's degree in Electrical Engineering, Mechanical Engineering, Industrial Engineering, or a related field. A minimum of 7 years of hands-on experience in industrial automation engineering, with a strong focus on PLC programming, HMI development, and robotic integration, is required. Proven experience with SCADA systems and industrial networking protocols is essential. Knowledge of safety standards (e.g., ISO 13849) and experience with simulation software are highly desirable. Excellent problem-solving skills, a meticulous attention to detail, and strong communication abilities are paramount for this role, especially given the remote nature of the position. The ability to manage projects independently and effectively coordinate with on-site teams is crucial. This is an excellent opportunity for a seasoned automation professional to contribute to cutting-edge manufacturing advancements. The role primarily supports facilities located in and around Kakamega, Kakamega, KE .
Senior Pharmaceutical Quality Assurance Manager
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Key responsibilities include overseeing all QA activities, such as batch record review and release, deviation management, change control, CAPA (Corrective and Preventive Actions) implementation, and internal audits. You will conduct thorough investigations into quality incidents, identify root causes, and implement effective corrective actions. This role involves significant interaction with regulatory bodies during inspections and ensuring the company remains audit-ready at all times. You will also lead and mentor a team of QA professionals, fostering a culture of quality and continuous improvement. Development and delivery of quality training programs to relevant personnel will also be part of your responsibilities.
The ideal candidate will possess a Master's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field. A minimum of 10 years of progressive experience in Quality Assurance within the pharmaceutical industry is required, with at least 5 years in a managerial or supervisory capacity. Extensive knowledge of GMP, GDP, and pharmaceutical regulatory landscapes (e.g., WHO, FDA, EMA guidelines) is essential. Proven experience in managing QMS, conducting audits, and leading regulatory inspections is a must. Excellent analytical, problem-solving, decision-making, and leadership skills are critical. Strong communication and interpersonal skills are necessary to effectively collaborate with cross-functional teams and external stakeholders remotely. This is an exceptional opportunity for a dedicated QA professional to lead quality initiatives and ensure the integrity of pharmaceutical products. The role supports operations in and around Nyeri, Nyeri, KE .
Senior Remote Automotive Quality Assurance Engineer
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Senior Industrial Automation Engineer
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Location: Mlolongo, Machakos, KE
Key Responsibilities:
- Design, develop, and implement PLC, SCADA, and HMI systems for industrial processes.
- Program and troubleshoot robotic systems and automated machinery.
- Specify and select industrial control hardware and components.
- Develop and maintain electrical schematics and control system documentation.
- Collaborate with cross-functional teams to integrate automation solutions into existing production lines.
- Perform root cause analysis for automation failures and implement corrective actions.
- Optimize existing automation systems for improved performance, efficiency, and reliability.
- Ensure compliance with industry safety standards and regulations.
- Provide technical leadership and mentorship to junior automation engineers.
- Bachelor's degree in Electrical Engineering, Mechanical Engineering, or a related field.
- Minimum of 6 years of experience in industrial automation engineering.
- Proficiency in programming various PLC platforms (e.g., Siemens, Allen-Bradley).
- Experience with SCADA system configuration and HMI development.
- Knowledge of industrial robotics and motion control systems.
- Strong understanding of electrical systems, instrumentation, and control theory.
- Excellent problem-solving, analytical, and troubleshooting skills.
- Ability to work effectively in a hybrid environment, balancing remote and on-site tasks.
Principal Industrial Process Engineer (Remote)
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Your responsibilities will include conducting detailed process mapping, simulation, and statistical analysis to pinpoint bottlenecks and inefficiencies. You will develop process improvement initiatives, which may involve re-engineering workflows, implementing new technologies, or optimizing equipment utilization. This role demands a strong understanding of Lean Manufacturing principles, Six Sigma methodologies, and advanced process control techniques. You will collaborate with cross-functional teams, including operations, R&D, and quality assurance, to ensure seamless integration of process changes. The ideal candidate is a strategic thinker with a proven ability to lead complex projects from conception to completion, delivering tangible business results. This is a fully remote opportunity, offering the flexibility to work from your preferred location.
Responsibilities:
- Analyze existing industrial processes to identify inefficiencies, bottlenecks, and areas for optimization in production, assembly, and supply chain operations.
- Design, develop, and implement new industrial processes and systems to improve efficiency, quality, safety, and cost-effectiveness.
- Utilize process simulation software, statistical analysis, and data visualization tools to model, analyze, and predict process performance.
- Lead and manage process improvement projects using methodologies such as Lean Manufacturing, Six Sigma, and Kaizen.
- Develop and implement standard operating procedures (SOPs) and best practices for industrial operations.
- Collaborate with engineering, manufacturing, and operations teams to troubleshoot process-related issues and implement corrective actions.
- Evaluate and recommend new technologies, equipment, and automation solutions to enhance industrial processes.
- Provide technical guidance and mentorship to junior engineers and operational staff.
- Conduct feasibility studies and cost-benefit analyses for proposed process changes and investments.
- Ensure all process designs comply with relevant industry regulations, safety standards, and environmental policies.
- Master's or Ph.D. in Industrial Engineering, Mechanical Engineering, Chemical Engineering, or a closely related field.
- 10+ years of progressive experience in industrial process engineering, with a focus on manufacturing or operations.
- Extensive experience with Lean Manufacturing, Six Sigma (Green Belt or Black Belt preferred), and other continuous improvement methodologies.
- Proficiency in process simulation software (e.g., Arena, AnyLogic) and statistical analysis tools (e.g., Minitab).
- Strong understanding of manufacturing operations, automation, and supply chain logistics.
- Excellent analytical, problem-solving, and project management skills.
- Proven ability to lead complex engineering projects and drive significant improvements.
- Exceptional communication and interpersonal skills, with the ability to influence stakeholders at all levels.
Senior Pharmaceutical Quality Assurance Specialist
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Responsibilities:
- Develop, implement, and maintain Quality Management Systems (QMS) in compliance with cGMP, ICH, and other relevant regulatory requirements.
- Conduct internal and external quality audits of manufacturing sites, suppliers, and contract organizations.
- Review and approve critical quality documents, including batch records, validation protocols, and change controls.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing CAPAs (Corrective and Preventive Actions).
- Oversee product release processes and ensure adherence to quality standards.
- Participate in regulatory inspections and facilitate responses to regulatory queries.
- Develop and deliver quality training programs to personnel.
- Monitor and assess supplier quality performance.
- Contribute to the qualification and validation of equipment, processes, and analytical methods.
- Stay current with evolving pharmaceutical regulations and industry best practices.
- Lead continuous improvement initiatives to enhance product quality and operational efficiency.
- Manage and mentor junior QA personnel.
- Prepare and present quality metrics and reports to senior management.
- Ensure the integrity and security of all quality-related data.
- Collaborate effectively with cross-functional teams, including R&D, manufacturing, and regulatory affairs.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 7 years of progressive experience in pharmaceutical Quality Assurance or Quality Control.
- In-depth knowledge of cGMP, ICH guidelines, and global pharmaceutical regulatory requirements.
- Proven experience in conducting GxP audits and managing QMS.
- Strong understanding of pharmaceutical manufacturing processes, validation, and laboratory controls.
- Excellent analytical, problem-solving, and decision-making skills.
- Exceptional attention to detail and ability to manage complex documentation.
- Strong written and verbal communication skills, with the ability to effectively communicate with regulatory bodies and stakeholders.
- Experience in handling regulatory inspections and submissions.
- Ability to work independently, manage priorities, and meet deadlines in a remote environment.
- Proficiency in quality management software and tools.
- Leadership experience is a strong asset.