60 Iso 9001 jobs in Bahrain

Job Description:

We are seeking a dedicated QA/QC Inspector to ensure that quality control systems are maintained in compliance with recognized industry practices and the Company’s Quality Control Manual. Candidates with bridge construction experience are preferred. A minimum of 5 years of experience in the construction industry is mandatory.

Responsibilities:

• Review and verify details of all tests and trials carried out, ensuring that methods used comply with standard procedures.
• Inspect technical details and collaborate with the QA/QC Engineer to identify any discrepancies where tolerances exceed design parameters or could affect operational performance.
• Ensure adherence to quality standards throughout all phases of construction activities.
• Maintain accurate records of inspections, tests, and quality reports in accordance with company policies.

Requirements:

• Bachelor’s degree or Diploma in Civil Engineering, Construction, or a related field.
• Minimum 5 years of experience in the construction industry, preferably with bridge projects.
• Knowledge of quality control standards, practices, and testing methods.
• Strong attention to detail, analytical skills, and the ability to identify and resolve issues proactively.
• Excellent communication and reporting skills.

Certifications:

• Relevant quality or construction certifications (preferred).

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with Good Manufacturing Practices (GMP), Good Clinical Practices (GCP), and other relevant regulations.
• Conduct internal audits and inspections to assess compliance with established quality standards and identify areas for improvement.
• Review and approve batch records, validation protocols, and other quality-related documentation.
• Investigate deviations, out-of-specification results, and customer complaints, implementing corrective and preventive actions (CAPA).
• Participate in external audits by regulatory agencies and customers.
• Manage change control processes, ensuring all changes are properly evaluated, documented, and implemented.
• Develop and deliver quality training programs to personnel across the organization.
• Monitor key quality metrics and provide regular reports to management.
• Stay up-to-date with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
• Contribute to the continuous improvement of quality processes and systems.
• Support the qualification and validation of equipment, processes, and analytical methods.
• Review and approve raw material and finished product testing results.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related science field.
• Minimum of 4 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry.
• Strong understanding of GMP, ISO, and other relevant regulatory guidelines.
• Experience with QMS implementation and maintenance.
• Proficiency in conducting audits, investigations, and managing CAPA systems.
• Excellent attention to detail, analytical skills, and problem-solving abilities.
• Strong written and verbal communication skills, with the ability to document findings clearly and concisely.
• Ability to work independently and collaboratively in a team environment.
• Familiarity with pharmaceutical manufacturing processes is a plus.
• Proficiency in Microsoft Office Suite and quality management software.
• Relevant professional certifications are an advantage.

• Develop and execute quality assurance plans and procedures for automotive products.
• Conduct inspections and testing of components, sub-assemblies, and finished products.
• Analyze test data and performance metrics to identify defects and areas for improvement.
• Work closely with R&D, engineering, and production teams to implement corrective and preventive actions (CAPA).
• Manage non-conformance reporting and resolution processes.
• Ensure compliance with automotive quality standards and customer specifications.
• Participate in internal and external audits.
• Develop and maintain quality documentation, including reports, procedures, and work instructions.
• Conduct root cause analysis for quality issues and implement effective solutions.
• Contribute to continuous improvement initiatives within the manufacturing process.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with regulatory requirements (e.g., GMP, ISO).
• Conduct internal audits and inspections to assess compliance with established quality standards and identify areas for improvement.
• Review and approve batch records, validation reports, and other quality-related documentation.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, determining root causes and implementing corrective and preventive actions (CAPAs).
• Participate in external audits and regulatory inspections, serving as a subject matter expert.
• Develop and deliver quality training programs for relevant personnel.
• Monitor quality metrics and key performance indicators (KPIs), reporting on trends and recommending improvements.
• Ensure that all manufacturing processes and products meet predefined quality standards and regulatory requirements.
• Manage change control processes, evaluating the impact of proposed changes on product quality.
• Stay up-to-date with current pharmaceutical quality regulations and industry best practices.
• Collaborate with various departments, including R&D, manufacturing, and regulatory affairs, to ensure a cohesive approach to quality.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related Life Science field.
• Minimum of 4 years of experience in a Quality Assurance role within the pharmaceutical industry.
• Strong understanding of Good Manufacturing Practices (GMP) and other relevant quality regulations.
• Experience with internal and external audits, regulatory inspections, and QMS implementation.
• Proficiency in deviation investigation, root cause analysis, and CAPA development.
• Excellent analytical, problem-solving, and decision-making skills.
• Strong attention to detail and commitment to accuracy.
• Effective communication and interpersonal skills, with the ability to collaborate cross-functionally.
• Experience with validation processes (e.g., process validation, cleaning validation) is a plus.
• Familiarity with documentation control systems and batch record review.

• Develop, implement, and maintain a comprehensive Quality Management System (QMS) compliant with relevant industry standards (e.g., ISO 9001).
• Establish quality control procedures and standards for raw materials, in-process production, and finished goods.
• Lead and manage the QA team, providing training, guidance, and performance evaluations.
• Oversee all quality inspection and testing activities, ensuring accuracy and adherence to protocols.
• Analyze production data to identify trends, root causes of defects, and areas for improvement.
• Implement corrective and preventive actions (CAPA) to address quality issues and prevent recurrence.
• Conduct internal audits of manufacturing processes and quality systems to ensure compliance.
• Collaborate with production, engineering, and R&D teams to integrate quality considerations into product development and process design.
• Manage customer complaints and returns related to product quality, ensuring timely and effective resolution.
• Ensure compliance with all regulatory requirements and industry-specific standards.
• Develop and deliver quality training programs for all manufacturing personnel.
• Maintain all quality-related documentation, records, and reports.
• Stay current with industry best practices and emerging quality management techniques.
• Manage relationships with external auditors and regulatory bodies.
• Drive a culture of quality excellence throughout the organization.

• Bachelor's degree in Engineering (Mechanical, Industrial, or Chemical), Quality Management, or a related scientific field.
• A minimum of 6-8 years of progressive experience in Quality Assurance within a manufacturing environment.
• Proven experience in implementing and managing ISO 9001 or similar quality management systems.
• Strong understanding of manufacturing processes, statistical process control (SPC), and quality control methodologies.
• Excellent leadership, team management, and coaching skills.
• Proficiency in data analysis tools and techniques.
• Strong problem-solving abilities and a systematic approach to identifying root causes.
• Excellent written and verbal communication skills, with the ability to present complex information clearly.
• Familiarity with Lean Manufacturing or Six Sigma principles is a significant plus.
• Attention to detail and a commitment to maintaining high-quality standards.
• Ability to work effectively in a demanding manufacturing environment.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with cGMP and other relevant regulatory guidelines.
• Oversee all quality assurance activities, including batch record review, deviation investigations, change control, and CAPA management.
• Conduct internal audits and host regulatory inspections from bodies such as the FDA, EMA, and local authorities.
• Manage and mentor a team of Quality Assurance professionals, fostering a culture of quality and continuous improvement.
• Ensure that all pharmaceutical products manufactured meet established quality and regulatory standards.
• Review and approve validation protocols and reports for manufacturing processes, equipment, and analytical methods.
• Collaborate with Production, R&D, and other departments to resolve quality issues and implement corrective actions.
• Maintain comprehensive documentation and records, ensuring data integrity and traceability.
• Stay updated on evolving pharmaceutical regulations and industry best practices.
• Lead continuous improvement initiatives to enhance product quality and operational efficiency.

• Develop, implement, and manage the company's overall Quality Management System (QMS).
• Establish and monitor quality control standards and procedures for all stages of the manufacturing process.
• Lead and mentor the Quality Assurance team, fostering a culture of quality and continuous improvement.
• Conduct internal audits and facilitate external audits by regulatory bodies and customers.
• Analyze quality data, identify trends, and implement corrective and preventive actions (CAPA).
• Oversee product testing and validation processes to ensure compliance with specifications.
• Manage supplier quality, including audits and performance evaluation.
• Develop and deliver quality training programs for all employees.
• Stay current with industry best practices, regulatory requirements, and new technologies in quality assurance.
• Collaborate with R&D, production, and other departments to ensure quality is integrated into all aspects of product development and manufacturing.
• Manage documentation control and ensure adherence to ISO standards or other relevant certifications.

• Bachelor's degree in Engineering, Science, or a related field. A Master's degree is preferred.
• Minimum of 7 years of experience in Quality Assurance or Quality Control within a manufacturing environment.
• Proven experience in developing and implementing QMS (e.g., ISO 9001).
• Strong knowledge of quality tools and methodologies (e.g., Six Sigma, Lean Manufacturing, SPC).
• Excellent leadership, team management, and problem-solving skills.
• Proficiency in data analysis and reporting.
• Strong understanding of manufacturing processes and product development lifecycles.
• Excellent communication, interpersonal, and presentation skills.
• Experience with regulatory compliance and certifications relevant to the manufacturing sector.
• Ability to drive change and foster a quality-focused culture.