41 Quality Assurance jobs in Bahrain

To ensure compliance with regulatory requirements and industry standards based on the responsibility of the company in the logistics chain for all the products in the warehouse and to provide solutions on the day-to-day operation.

As part of the DSV team, Associates are expected to meet company objectives in the areas of performance, safety, and quality. Associates are expected to comply with all corporate and site-specific policies.

1. Plan management needs to comply with regulatory requirements and standards of the industry in force within the framework of the Quality Management System.
2. Ensure the documentation, traceability, and approval necessary for compliance with the regulatory requirements in the company's logistics chain (storage, packaging, dispatch, distribution) of products available at the warehouse.
3. Serve and advise interested parties (clients, local authorities, suppliers, workers, corporate) on issues related to compliance with regulatory requirements and current industry standards within the framework of the Quality Management System.
4. Clean and comply with the organization of the warehouse and/or warehouse in compliance with the 5S program.
5. Assist operations by tracking, documenting, and reporting quality levels as well as CSR, environmental, and health and safety KPIs.
6. Develop or update procedures for capturing, investigating, and documenting product complaints.
7. Monitor risk-management procedures, maintain problem logs, and report issues to managers and product developers.
8. Provide training and support to quality assurance team members that covers systems, policies, procedures, and core processes.
9. Ensure all relevant QHSE systems are implemented and practiced as ISO standards and legal requirements on all DSV Bahrain operational facilities.
10. Data collection and analysis by way of weekly/monthly/quarterly/yearly statistics reports.
11. Assist Top Management in identifying any process gaps within the organization.
12. Frequently visit the company’s facilities and conduct observation tours, HSE walk, HSE inspections, and implement other relevant HSE implementation tools.
13. Work as an internal auditor for conducting IMS audits.
14. Collaborate with the inventory department for conducting cyclical stock counts to maintain stock integrity and ensure that financial stock takes and stock counts are conducted according to client contracts and DSV cyclical requirements.
15. Perpetually follow up on discrepancies, non-conformities, and report on developments.

Qualifications:

Graduate in any discipline/ Diploma or Certificate holder.

Experience:

Minimum of 1-3 years in a Quality Assurance field, Inventory, or customer service environment within Logistics.

Preferred Qualifications:

• 1-3 years warehouse/logistics support experience.
• 2-3 years’ experience in a Quality Assurance-related capacity.

• Proficient with MS Office Applications.
• WMS functions.

• Business writing proficiency.

• Intermediate level to verify quantities of product, count inventory, or perform other duties associated with handling, storing, and distributing client products.

• Strong attention to detail and accuracy, accomplishing job tasks in a timely manner.
• Ability to perform duties with minimal supervision or guidance.
• Ability to multi-task.
• Must be able to effectively adapt to change and thrive in a stimulating, fast-paced work environment.

Full Time

• Logistics
• Transportation
• Warehousing
• Courier

• HSE (Health and Safety)

• Quality Assurance
• QA
• Quality Management
• Food Safety
• Safety Management
• Safety Audit
• HSE
• IMS
• Audit
• Warehouse Safety

Department: Finance / Procurement

Venue: Exhibition World Bahrain

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ASM Global teams across the world are innate problem solvers and people who thrive on the excitement of developing events that create opportunity and connection. We are meticulous planners, innovative thinkers, relationship specialists, and experienced business leaders who love what they do.

At ASM Global, we love events; it's in our DNA and what drives us. The role involves developing and implementing quality management systems, conducting audits, and ensuring compliance with internal and external quality standards.

Every day, our people are responsible for delivering extraordinary experiences for every guest who walks through our doors. You will share our values, have a people-centric mindset, and genuinely want to make a difference. This makes you stand out from the crowd, and we want to meet you.

You will be detail-oriented, adaptable, and committed to continuous improvement, ensuring that excellence is embedded in every aspect of our operations.

Inaugurated in November 2022 and owned by the Bahrain Tourism and Exhibitions Authority (BTEA), Exhibition World Bahrain (EWB) is the world’s leading new exhibition and convention venue for 2023, and the Middle East's leading large-scale wedding venue for 2024. It is the newest MICE venue in the Middle East, offering a wide range of leasable spaces for all types of events, from large conventions and exhibitions to conferences, meetings, entertainment performances, weddings, galas, and corporate functions.

The venue features 10 large exhibition halls, a convention centre with a grand hall, and 19 meeting rooms of varying sizes. Its extensive capacity enables hosting multiple events simultaneously. The new Exhibition World Bahrain will be the largest venue of its kind in the Middle East, offering 95,000 sqm of exhibition space, a 4,000-seat tiered auditorium, 95 meeting rooms, a Royal & VIP Majlis, supported by event organizers' offices, and a 250-seat restaurant.

ASM Global is the world's leading producer of entertainment experiences, specializing in venue and event strategy and management. It delivers locally tailored solutions and cutting-edge technologies to maximize guest experiences. Its elite venue network spans five continents, including over 350 prestigious venues such as Moscone Center San Francisco, ICC Sydney, Olympia London, Coca-Cola Arena Dubai, RAC Arena Perth, Cairns Convention Centre, and Brisbane Convention and Exhibition Centre.

ASM Global aims to be a true employer of choice, providing long-term careers and development opportunities. Follow us on Facebook, Instagram, LinkedIn, and X at asmglobal.com.

Working in the venue and event industry requires supporting the delivery of events throughout the year, including weekends, evenings, and public holidays.

This role is managed directly by us; no recruitment agencies, please.

Download Job Description (PDF)

• Perform routine inspections and quality checks on raw materials, in-process products, and finished goods.
• Conduct various tests (e.g., dimensional, functional, visual) using appropriate measurement tools and equipment.
• Identify and document non-conformities, defects, and deviations from quality standards.
• Generate detailed quality reports and maintain accurate records of inspection results.
• Collaborate with production teams to identify root causes of quality issues and implement corrective and preventive actions (CAPA).
• Assist in the development and revision of quality control procedures and documentation.
• Ensure compliance with ISO standards and other relevant industry regulations.
• Calibrate and maintain testing equipment to ensure accuracy and reliability.
• Participate in internal and external quality audits.
• Provide training and guidance to production staff on quality procedures and best practices.

• Associate's degree or Diploma in a technical field (e.g., Manufacturing, Engineering Technology, Quality Management).
• Minimum of 2-4 years of experience in a Quality Assurance or Quality Control role within a manufacturing environment.
• Strong understanding of quality management systems (e.g., ISO 9001).
• Proficiency in using various measurement tools (e.g., calipers, micrometers, gauges).
• Excellent attention to detail and strong analytical skills.
• Ability to read and interpret technical drawings and specifications.
• Good communication and interpersonal skills, with the ability to work effectively with production teams.
• Basic computer proficiency (Microsoft Office Suite).
• Knowledge of statistical process control (SPC) is a plus.
• Fluency in English is required; Arabic is an advantage.

• Develop, implement, and monitor quality control plans, procedures, and inspection criteria for all stages of the manufacturing process.
• Conduct regular quality audits of production lines, raw materials, and finished products to identify non-conformities and deviations.
• Analyze quality data, identify root causes of defects, and implement corrective and preventive actions (CAPA).
• Collaborate with design, production, and supply chain teams to ensure quality requirements are integrated throughout the product lifecycle.
• Establish and maintain quality documentation, including inspection reports, test data, and quality manuals.
• Oversee the calibration and maintenance of quality testing equipment.
• Train production staff on quality standards, procedures, and best practices.
• Manage supplier quality by conducting supplier audits and evaluating material quality.
• Lead and participate in continuous improvement initiatives, such as Lean Manufacturing or Six Sigma projects, to enhance product quality and process efficiency.

• Bachelor's degree in Engineering (Mechanical, Industrial, or Electrical) or a related technical field.
• Minimum of 3-5 years of experience in Quality Assurance or Quality Control within a manufacturing environment.
• Strong knowledge of quality management systems (e.g., ISO 9001) and industry standards.
• Proficiency in quality tools and methodologies (e.g., FMEA, SPC, 8D, PPAP).
• Certifications such as ASQ Certified Quality Engineer (CQE) or Six Sigma Green/Black Belt are highly desirable.

• Implement, maintain, and continuously improve the Quality Management System (QMS) in accordance with GMP, GLP, and other relevant regulatory guidelines.
• Review and approve batch production records, analytical data, and other manufacturing documentation to ensure compliance with specifications.
• Conduct internal and external audits of facilities, processes, and suppliers to assess compliance and identify areas for improvement.
• Investigate quality deviations, non-conformances, and customer complaints, leading root cause analysis and CAPA implementation.
• Oversee the change control process, ensuring all changes to processes, equipment, or materials are properly documented and approved.
• Participate in risk assessments and quality reviews for new products, processes, and equipment.
• Provide quality assurance training to production and laboratory personnel.
• Ensure proper documentation and control of quality-related documents, including SOPs, policies, and specifications.
• Prepare and present quality reports for management review, highlighting key trends and issues.
• Stay current with evolving pharmaceutical regulations and industry best practices.

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, or a related scientific or engineering field.
• Minimum of 3-5 years of experience in Quality Assurance within a pharmaceutical manufacturing environment.
• In-depth knowledge of Good Manufacturing Practices (GMP), ISO standards, and relevant international pharmaceutical regulations (e.g., FDA, EMA).
• Experience with QMS implementation, audit management, and CAPA processes.
• Strong analytical and problem-solving skills with meticulous attention to detail.
• Excellent written and verbal communication skills for documentation and cross-functional collaboration.
• Ability to work independently and as part of a collaborative team in a highly regulated environment.
• Proficiency in quality management software and Microsoft Office Suite.
• Fluency in English is essential; Arabic is a plus.

• Plan, coordinate, and monitor clinical trials according to study protocols and regulatory guidelines.
• Ensure adherence to Good Clinical Practice (GCP), local regulations, and Standard Operating Procedures (SOPs).
• Conduct site visits, source data verification, and ensure data integrity.
• Manage essential trial documents and maintain accurate records.
• Collaborate with investigators, research staff, and sponsors.
• Identify and resolve issues related to trial conduct, patient safety, and data quality.
• Prepare study reports, summaries, and presentations for internal and external stakeholders.

• Bachelor's degree in Life Sciences, Pharmacy, Nursing, or a related health-scientific field.
• 1-3 years of experience as a Clinical Research Associate or in a similar clinical research role.
• Strong knowledge of ICH-GCP guidelines and relevant regulatory requirements.
• Excellent organizational skills and attention to detail for data collection and documentation.
• Ability to travel to clinical sites as required.
• Strong communication and interpersonal skills to interact with investigators and study staff.
• Proficiency in using Electronic Data Capture (EDC) systems and clinical trial management software.

• Ensure strict compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and Good Documentation Practices (GDP) across all manufacturing, testing, and distribution processes.
• Conduct regular internal and external quality audits of manufacturing facilities, suppliers, and contract manufacturers to assess compliance with regulatory requirements and internal quality standards.
• Review and approve batch records, analytical data, and other documentation to ensure accuracy, completeness, and adherence to specifications before product release.
• Investigate quality deviations, non-conformances, and customer complaints, identifying root causes and implementing effective corrective and preventive actions (CAPA).
• Manage and maintain the company's Quality Management System (QMS), including documentation control, change control, and training records.
• Participate in the qualification and validation of equipment, processes, and cleaning procedures.
• Develop, review, and revise Standard Operating Procedures (SOPs), quality policies, and other quality-related documents.
• Provide quality assurance oversight and guidance to production, laboratory, and other relevant departments.
• Prepare for and participate in regulatory inspections by local and international health authorities.
• Monitor and analyze quality metrics, identifying trends and recommending improvements to enhance product quality and process efficiency.
• Conduct training sessions for staff on GMP principles, quality procedures, and regulatory updates.
• Collaborate with cross-functional teams to implement quality initiatives and resolve quality-related issues.
• Stay informed about changes in pharmaceutical regulations and industry best practices.
• Manage supplier quality agreements and perform supplier qualifications.

• Bachelor's degree in Pharmacy, Chemistry, Biochemistry, Life Sciences, or a related scientific discipline.
• Minimum of 3 years of direct experience in a Quality Assurance role within the pharmaceutical or biopharmaceutical industry.
• In-depth knowledge and practical application of GMP, GLP, ICH guidelines, and relevant international pharmaceutical regulations (e.g., FDA, EMA).
• Experience with quality management systems (QMS), including deviation management, CAPA, change control, and document control.
• Strong analytical and problem-solving skills, with a keen eye for detail and accuracy.
• Excellent written and verbal communication skills, capable of preparing clear, concise reports and effectively communicating complex quality issues.
• Ability to conduct effective audits and implement corrective actions.
• Proficiency in Microsoft Office Suite and quality management software.
• Highly organized, meticulous, and capable of managing multiple priorities in a dynamic environment.
• A proactive and independent work ethic, coupled with strong teamwork capabilities.

• Perform comprehensive quality inspections of incoming raw materials, in-process components, and finished products according to established specifications and standards.
• Utilize precision measuring instruments (e.g., calipers, micrometers, gauges, CMM) to verify dimensions and tolerances.
• Conduct visual inspections to identify defects, blemishes, or non-conformities.
• Document inspection results accurately, including recording data, preparing reports, and maintaining inspection logs.
• Identify and segregate non-conforming materials or products, initiating corrective action requests (CARs).
• Work collaboratively with production, engineering, and supply chain teams to investigate root causes of defects and implement preventative measures.
• Ensure calibration and proper functioning of inspection equipment.
• Participate in the development and improvement of quality control procedures and inspection plans.
• Adhere to all safety regulations and quality management system (QMS) requirements (e.g., ISO 9001).
• Assist in internal and external quality audits.
• Provide feedback to production personnel on quality issues and best practices.

• Technical diploma or vocational training in Quality Control, Manufacturing, Mechanical Engineering, or a related field.
• Minimum of 3-5 years of experience as a Quality Assurance Inspector in a manufacturing environment.
• Strong proficiency in using a wide range of precision measuring instruments.
• Ability to read and interpret engineering drawings, blueprints, and technical specifications (including GD&T).
• Solid understanding of quality control principles and methodologies (e.g., SPC, 5S, Lean Manufacturing).
• Familiarity with Quality Management Systems (QMS) such such as ISO 9001.
• Excellent attention to detail and strong analytical skills.
• Good written and verbal communication skills in English (Arabic is a plus).
• Ability to work independently and as part of a team in a fast-paced production environment.
• Strong problem-solving abilities to identify and resolve quality issues.
• Basic computer skills for data entry and report generation.

• Develop, implement, and maintain the Quality Management System (QMS) in accordance with cGMP, international standards (e.g., ISO, ICH), and local regulatory requirements.
• Conduct regular quality audits (internal and external) to ensure compliance with established procedures and regulations.
• Review and approve batch production records, analytical data, and other critical documentation to ensure product release readiness.
• Manage deviations, non-conformances, CAPAs (Corrective and Preventive Actions), and change controls, ensuring timely closure and effectiveness.
• Participate in risk assessments and root cause analysis for quality-related issues.
• Oversee validation activities for processes, equipment, and analytical methods.
• Ensure proper documentation control, including SOPs, specifications, and master batch records.
• Collaborate with manufacturing, R&D, and regulatory affairs departments to address quality-related concerns and drive continuous improvement.
• Provide quality training to personnel across various departments.
• Prepare and review quality metrics and trends, presenting findings to management.
• Handle customer complaints and product recalls in accordance with established procedures.
• Liaise with regulatory agencies during inspections and provide necessary documentation.
• Stay informed about the latest pharmaceutical regulations and industry best practices.
• Manage stability studies and ensure data integrity.

• Bachelor's degree in Pharmacy, Pharmaceutical Sciences, Chemistry, Biotechnology, or a related scientific field.
• Minimum of 4-6 years of experience in Quality Assurance within the pharmaceutical manufacturing industry.
• In-depth knowledge of cGMP regulations (e.g., FDA, EMA, PIC/S) and relevant quality standards.
• Proven experience with QMS, deviation management, CAPA, change control, and documentation control.
• Strong analytical skills and attention to detail.
• Excellent written and verbal communication skills in English; Arabic is a plus.
• Ability to work independently and collaboratively in a highly regulated environment.
• Problem-solving aptitude with a proactive and methodical approach.
• Proficiency in Microsoft Office Suite and quality management software.
• Experience with laboratory information management systems (LIMS) is an advantage.

• Competitive salary and comprehensive benefits package.
• A critical role contributing to public health and safety.
• Opportunities for professional growth and specialized training.
• A highly professional, ethical, and collaborative work environment.
• Exposure to advanced pharmaceutical manufacturing processes.