What Jobs are available for Clinical Quality in Bahrain?

• Bachelor's degree in Engineering (Mechanical, Electrical, Biomedical) or a related scientific field.
• Minimum of 5-7 years of experience in Quality Assurance within the medical device industry.
• In-depth knowledge of quality management systems (QMS), such as ISO 13485 and FDA 21 CFR Part 820.
• Proven experience with risk management principles (e.g., ISO 14971).
• Demonstrated experience in validation and verification activities (IQ, OQ, PQ).
• Strong understanding of manufacturing processes and statistical quality control.
• Excellent analytical and problem-solving skills, with a strong attention to detail.
• Proficiency in developing and implementing CAPA systems.
• Effective communication and interpersonal skills, with the ability to collaborate across departments.
• Experience preparing for and participating in regulatory audits.

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with relevant regulations (e.g., ISO 13485, FDA 21 CFR Part 820).
• Oversee all aspects of QA operations, including document control, change control, CAPA, audits, and risk management.
• Lead internal and external audits, ensuring regulatory compliance and identifying areas for improvement.
• Manage the complaint handling and adverse event reporting processes.
• Develop and execute validation and verification protocols for software and hardware components.
• Collaborate with R&D, Engineering, Manufacturing, and Regulatory Affairs teams to ensure quality is integrated throughout the product lifecycle.
• Establish quality metrics and key performance indicators (KPIs), monitoring trends and implementing corrective actions.
• Provide training and guidance to personnel on QMS requirements and quality best practices.
• Lead continuous improvement initiatives to enhance product quality and process efficiency.
• Review and approve product release documentation.
• Manage supplier quality and conduct supplier audits.
• Represent the company during regulatory inspections.
• Effectively manage and mentor a remote QA team, fostering a culture of quality excellence.

• Bachelor's degree in Engineering, Science, or a related technical field. A Master's degree is preferred.
• Minimum of 8 years of progressive experience in Quality Assurance within the medical device industry.
• Extensive knowledge of ISO 13485, FDA 21 CFR Part 820, and other relevant medical device regulations.
• Proven experience in developing and maintaining a comprehensive QMS.
• Strong understanding of product development lifecycle for medical devices.
• Experience with risk management (ISO 14971) and CAPA processes.
• Excellent analytical, problem-solving, and decision-making skills.
• Demonstrated leadership and team management abilities, particularly in a remote setting.
• Exceptional communication, interpersonal, and documentation skills.
• Proficiency in quality management software and tools.
• Ability to work independently and manage multiple priorities in a fast-paced environment.
• Proficiency in English; knowledge of other languages is a plus.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with relevant regulations (e.g., FDA 21 CFR Part 820, ISO 13485).
• Create and execute comprehensive test plans, protocols, and reports for medical devices.
• Perform root cause analysis of non-conformances and implement corrective and preventive actions (CAPA).
• Conduct internal and external audits to ensure compliance with quality standards and regulatory requirements.
• Review and approve design control documentation, validation reports, and manufacturing processes.
• Collaborate with R&D and engineering teams to ensure design outputs meet specifications and quality objectives.
• Manage supplier quality and conduct supplier audits as necessary.
• Participate in regulatory submissions and inspections.
• Train and mentor junior QA personnel.
• Drive continuous improvement initiatives within the quality assurance framework.

• Bachelor's degree in Engineering (Biomedical, Mechanical, Electrical), Science, or a related field.
• 5+ years of experience in Quality Assurance within the medical device or pharmaceutical industry.
• Thorough understanding of FDA regulations, ISO 13485, and other relevant international standards.
• Proven experience in developing and implementing QMS, CAPA, and risk management processes.
• Strong analytical, problem-solving, and investigative skills.
• Excellent documentation and technical writing abilities.
• Experience with statistical methods and tools for quality control.
• Proficiency in quality assurance software and tools.
• Ability to work independently and collaboratively in a remote team environment.
• Strong attention to detail and commitment to accuracy.

• Develop, implement, and maintain quality assurance systems and procedures for medical device products.
• Create and execute comprehensive validation and verification plans for new and existing products.
• Conduct thorough risk assessments and implement mitigation strategies in accordance with ISO 14971.
• Ensure compliance with relevant regulatory standards, including FDA QSR, ISO 13485, and CE Marking requirements.
• Manage and oversee the CAPA (Corrective and Preventive Actions) process, including investigation and closure.
• Review and approve product design documentation, manufacturing records, and change control requests.
• Conduct internal audits and support external audits from regulatory bodies and customers.
• Collaborate with cross-functional teams to address quality issues and implement continuous improvement initiatives.
• Train and mentor junior quality assurance personnel.
• Stay up-to-date with evolving regulatory requirements and industry best practices in medical device quality assurance.

• Bachelor's degree in Engineering (Biomedical, Mechanical, Electrical) or a related scientific field.
• Minimum of 6 years of experience in Quality Assurance within the medical device industry.
• In-depth knowledge of ISO 13485, FDA 21 CFR Part 820, and other relevant medical device regulations.
• Proven experience in developing and executing validation and verification protocols.
• Strong understanding of risk management principles and tools (e.g., FMEA).
• Experience with CAPA, change control, and non-conformance management systems.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong written and verbal communication skills, with the ability to document and present findings effectively.
• Ability to work independently and manage projects effectively in a remote environment.

Company Description

JUNAID FOR PERFUMES LIMITED is a facilities services company based out of Station Way, Crawley, England, United Kingdom.

Role Description

This is a full-time on-site role for a Quality Assurance Quality Control professional at JUNAID FOR PERFUMES LIMITED located in Muharraq Governorate, Bahrain. The role will involve day-to-day tasks associated with quality control, quality assurance, quality management, and quality auditing.

Qualifications

• Quality Control and Quality Assurance skills
• Experience in Quality Management and Good Manufacturing Practice (GMP)
• Skills in Quality Auditing
• Understanding of regulatory requirements in the perfume industry
• Strong attention to detail and analytical skills
• Excellent communication and teamwork abilities
• Bachelor's degree in Quality Assurance, Chemistry, or related field

QA/QC Specialist: Joinery and Furniture Manufacturing

We're looking for a skilled QA/QC Specialist to join our team and ensure every product that leaves our workshop meets our rigorous standards for excellence.

Key Responsibilities:

Quality Control: Conduct thorough inspections of raw materials, in-process goods, and finished products to identify defects, deviations, and non-conformities.

Process Improvement: Work closely with our production and design teams to identify root causes of quality issues and implement corrective and preventive actions.

Documentation: Maintain detailed records of all inspections, tests, and quality reports, including non-conformance reports (NCRs).

Standard Adherence: Ensure all products and processes comply with company quality standards, project specifications, and industry regulations.

Supplier Relations: Conduct audits and inspections of incoming materials from suppliers to ensure they meet our quality requirements.

Qualifications and Skills:

Proven experience in a QA/QC role within the joinery, cabinetry, or furniture manufacturing industry is essential.

Deep knowledge of wood, veneers, laminates, and other common materials used in furniture production.

Strong understanding of manufacturing and assembly processes, including cutting, joining, finishing, and hardware installation.

Exceptional attention to detail and a critical eye for precision.

Excellent communication skills for collaborating with team members and addressing quality issues.

Proficiency in reading and interpreting technical drawings, blueprints, and project specifications.

Job Type: Full-time

What will you contribute? Reporting to the QA Manager, the QA engineer will be involved in creating and executing product test plans to ensure software products meet design specifications and product quality standards. Assists Development team with process improvements to improve product quality.

Responsibilities & Deliverables: Your deliverables as a QA Engineer will include, but are not limited to, the following:

• Create test cases from product specifications.
• Execute test plans and test cases and compile results.
• Set up and maintain testing environment.
• Assist in the review of software development processes to improve product quality.
• Track defects from detection to resolution and works with developers to reproduce and resolve defects.
• Communicates with stakeholders on product issues.
• Acquire and maintain knowledge of existing products, operations or systems.
• Review product documentation to ensure completeness and accuracy.
• Provide support to stakeholders prior to release of software.
• Create and/or run database scripts to populate data and validate test results.
• Create and design test cases and maintain test library
• Design, develop, and maintain test scripts to be automated.

Provide testing effort estimates for enhancements.

Required Experience:

• Minimum 3 years' experience in software testing or related field.
• Working experience in Banking/Financial domain preferred
• Hands on experience: DML(Data Manipulation Language) commands with any listed databases (Microsoft SQL, Oracle, PostgreSQL)
• Java, C# (hands on experience with Java applications)
• Proficiency with Microsoft Office and Linux applications
• Effective verbal and written communication skills; effective customer service skills.
• Ability to work independently or within a team environment and handle multiple projects simultaneously.
• Knowledge of quality assurance methods and techniques including the software development lifecycle.
• Effective planning and organizational skills, with an attention to detail.
• Effective analytical and problem-solving skills and ability to think 'out of the box' for process improvements.
• Ability to work with specialized software tools such as (Jenkins, Bit bucket, Github, JIRA, Selenium, QTP, Visual Studio Test Suit); effectively implement and evaluate new processes or plans.
• Ability to execute test plans and test scripts for commercial software applications, document expected results vs. actual results, and record software defects.
• Preferred knowledge of the Agile software development methodology
• Knowledge of market infrastructures
• Knowledge of automated testing software tools with ability to design and develop automated testing programs
• Performance/Load testing experience and knowledge

Company Description

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Role Description

This is a full-time on-site role for a Quality Assurance Officer located in Manama. The Quality Assurance Officer will be responsible for overseeing the implementation and maintenance of quality assurance processes. Duties include conducting quality audits, ensuring compliance with regulations, analyzing data to identify areas for improvement, and managing quality control procedures.

Qualifications

• Experience in Quality Assurance and Quality Management
• Proficiency in Quality Control and Quality Auditing
• Strong Analytical Skills
• Excellent attention to detail and problem-solving skills
• Ability to work collaboratively in a team environment
• Bachelor's degree in a related field is preferred
• Experience in the manufacturing industry is a plus

• Develop and implement quality assurance plans and procedures.
• Conduct in-process and final product inspections to ensure compliance with specifications.
• Analyze production data to identify trends and areas for quality improvement.
• Perform root cause analysis for quality defects and implement corrective actions.
• Collaborate with engineering and production teams to resolve quality issues.
• Maintain quality records and documentation.
• Operate and calibrate testing equipment.
• Ensure adherence to relevant industry standards and regulatory requirements.
• Participate in internal and external audits.
• Contribute to the continuous improvement of quality management systems.
• Train production staff on quality standards and procedures.

• Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or a relevant technical discipline.
• 3-5 years of experience in quality assurance or quality control within a manufacturing environment.
• Solid understanding of quality management systems (e.g., ISO 9001).
• Experience with statistical process control (SPC) and quality tools (e.g., Six Sigma).
• Proficiency in using measurement and testing equipment.
• Strong analytical, problem-solving, and critical thinking skills.
• Excellent attention to detail and accuracy.
• Good communication and teamwork abilities.
• Familiarity with manufacturing processes and materials.