What Jobs are available for Medical Quality Assurance in Bahrain?

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

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with relevant regulatory standards (e.g., ISO 13485, FDA 21 CFR Part 820).
• Lead and manage the QA team, including performance management, training, and professional development.
• Oversee all quality assurance activities, including document control, change management, CAPA (Corrective and Preventive Actions), and internal audits.
• Conduct regular internal audits and support external audits by regulatory agencies and notified bodies.
• Ensure product conformity and compliance throughout the product lifecycle, from design and development to post-market surveillance.
• Review and approve product documentation, validation reports, and manufacturing batch records.
• Manage supplier quality, including qualification, auditing, and performance monitoring.
• Investigate and resolve quality issues, implementing effective corrective and preventive actions.
• Champion quality principles and foster a quality-conscious culture across all departments.
• Stay up-to-date with evolving regulatory requirements and industry best practices in medical device quality assurance.

• Bachelor's degree in Engineering, Science, or a related technical field. Advanced degree or relevant certifications (e.g., ASQ Certified Quality Engineer) are a strong plus.
• A minimum of 7 years of experience in quality assurance within the medical device or pharmaceutical industry.
• In-depth knowledge of ISO 13485, FDA QSR (21 CFR Part 820), and other relevant international quality standards.
• Proven experience in developing and managing QMS documentation and procedures.
• Demonstrated experience in leading audits, managing CAPA systems, and conducting risk assessments.
• Strong leadership, team management, and motivational skills.
• Excellent analytical, problem-solving, and decision-making abilities.
• Exceptional communication, interpersonal, and influencing skills.
• Proficiency in quality tools and software.
• Ability to work effectively in a hybrid environment, balancing on-site collaboration with remote responsibilities.

• 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.

Plans, coordinates, and directs quality control program designed to ensure continuous production of products consistent with established standards: Develops and analyzes statistical data and product specifications to determine present standards and establish proposed quality and reliability expectancy of finished product.  Formulates and maintains quality control objectives and coordinates objectives with production procedures in cooperation with other plant managers to maximize product reliability and minimize costs. Directs, through intermediate personnel, workers engaged in inspection and testing activities to ensure continuous control over materials, facilities, and products. lans, promotes, and organizes training activities related to product quality and reliability. ay investigate and adjust customer complaints regarding quality. pproves incoming materials by confirming specifications; conducting visual and measurement tests; rejecting and returning unacceptable materials. pproves in-process production by confirming specifications; conducting visual and measurement tests; communicating required adjustments to production supervisor. pproves finished products by confirming specifications; conducting visual and measurement tests; returning products for re-work; confirming re-work. ocuments inspection results by completing reports and logs; summarizing re-work and waste; inputting data into quality database. eeps measurement equipment operating by following operating instructions. Maintains safe and healthy work environment by following standards and procedures; complying with legal regulations. ccomplishes quality and organization mission by completing related results as needed.

For more info call please send your CV at

Job Type: Full-time

Experience:

• two: 1 year (Preferred)

Job Description:

We are seeking a
Senior QA/QC Engineer
with extensive experience in
road and infrastructure projects
. The ideal candidate will be
ISO 9001:2015 Lead Auditor/Internal Auditor certified
and will play a key role in ensuring that construction projects adhere to established quality standards and specifications. This position involves document control, inspections, compliance monitoring, and collaboration with project teams to maintain high-quality outcomes throughout the construction process.

Responsibilities:

• Develop and implement
  QA/QC plans, procedures, and inspection checklists
  .
• Ensure compliance with
  project specifications, codes, and standards
  .
• Conduct
  regular inspections and tests
  on materials, workmanship, and completed work.
• Analyze inspection results and identify
  areas for improvement
  .
• Collaborate with project teams to maintain
  consistent quality standards
  .

Skills and Qualifications:

• Extensive experience in
  construction quality assurance and control
  , particularly in
  road and infrastructure projects
  .
• ISO 9001:2015 Lead Auditor/Internal Auditor certification
  .
• Strong knowledge of relevant
  codes, standards, and regulations
  .
• Excellent
  analytical, problem-solving, and communication skills
  .

Company Description

Shafiq Glass, founded in 2005, has become a leading provider of high-quality aluminium and glass products in Bahrain. The company's modern fabrication plant meets international standards, emphasizing their commitment to quality and excellence. Specializing in doors, windows, storefronts, entrances, and more, Shafiq Glass is renowned for completing reputable projects across Bahrain. Their aluminum division offers a comprehensive selection of profiles for doors and windows, alongside the supply and installation of ACP for facades. Shafiq Glass consistently exceeds client expectations with high-quality products and services that meet industry standards.

Role Description

This is a full-time on-site role for a Quality Control Engineer, located in Al-Hidd. The Quality Control Engineer will be responsible for inspecting and assessing the quality of aluminium and glass products, ensuring they meet company and industry standards. Daily tasks include conducting tests, documenting quality issues, suggesting improvements, and collaborating with other departments to resolve quality-related problems. The role also involves maintaining quality control documentation and updating quality management systems.

Qualifications

• Skills in Quality Control and Quality Assurance
• Strong Analytical Skills for problem identification and resolution
• Effective Communication skills
• Experience in Quality Management processes and systems
• Excellent attention to detail and commitment to quality
• Relevant experience in the glass and aluminium industry is a plus
• Bachelor's degree in Engineering