31 Verification Engineer 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

• Develop, implement, and maintain the company's Quality Management System (QMS) in accordance with regulatory requirements (e.g., FDA, EMA, SFDA).
• Oversee all QA activities, including batch record review, deviation management, CAPA implementation, and change control.
• Conduct internal audits and host regulatory inspections, ensuring preparedness and successful outcomes.
• Manage and mentor the QA team, fostering a culture of quality and continuous improvement.
• Ensure that all pharmaceutical products meet established specifications and quality standards before release.
• Review and approve validation protocols and reports for manufacturing processes, equipment, and analytical methods.
• Collaborate with R&D, manufacturing, and regulatory affairs departments to ensure product quality throughout the lifecycle.
• Monitor and analyze quality metrics, identifying trends and implementing corrective and preventive actions.
• Manage supplier qualification programs and ensure the quality of procured raw materials and components.
• Stay current with evolving regulatory guidelines and industry best practices in pharmaceutical quality assurance.
• Maintain all quality-related documentation and records.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. A Master's degree is preferred.
• Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
• Proven experience in implementing and managing GMP-compliant QMS.
• In-depth knowledge of pharmaceutical manufacturing processes, analytical testing, and regulatory requirements.
• Strong leadership, management, and team-building skills.
• Excellent analytical, problem-solving, and decision-making abilities.
• Proficiency in regulatory documentation and reporting.
• Strong written and verbal communication skills.

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Job Summary:

We are looking for an experienced and results-driven Quality Manager to lead our quality assurance initiatives at Tafaseel BPO. The Quality Manager will be responsible for developing, implementing, and managing quality assurance processes to ensure that our BPO operations consistently meet and exceed client expectations and industry standards. This role is essential for maintaining a high level of service quality and operational efficiency.

Job Summary:

We are looking for an experienced and results-driven Quality Manager to lead our quality assurance initiatives at Tafaseel BPO. The Quality Manager will be responsible for developing, implementing, and managing quality assurance processes to ensure that our BPO operations consistently meet and exceed client expectations and industry standards. This role is essential for maintaining a high level of service quality and operational efficiency.

Key Responsibilities:

Quality Strategy Development: Design and implement a comprehensive quality assurance strategy aligned with organizational goals and client requirements.

Monitoring and Evaluation: Oversee the monitoring of service delivery processes, conducting regular evaluations and audits to ensure compliance with established quality standards.

Data Analysis: Analyze quality performance metrics and trends, preparing detailed reports to inform decision-making and continuous improvement initiatives.

Team Leadership: Lead and mentor the quality assurance team, fostering a culture of quality and accountability throughout the organization.

Feedback and Improvement: Provide constructive feedback and coaching to employees based on quality assessments, and collaborate with training teams to address skill gaps.

Process Enhancement: Identify opportunities for process improvements and implement best practices to enhance service quality and operational efficiency.

Client Liaison: Serve as the primary point of contact for quality-related client inquiries, addressing concerns and ensuring alignment with client expectations.

Compliance Assurance: Ensure adherence to regulatory and industry standards, conducting regular compliance audits and implementing corrective actions as necessary.

Stakeholder Collaboration: Work closely with cross-functional teams, including Operations, Training, and Client Services, to drive quality initiatives and improvements.

Qualifications:

Bachelor’s degree in business administration, Quality Management, or a related field; master’s degree is a plus.

Proven experience in quality management, preferably within the BPO industry, with a minimum of 3 years in a leadership role.

Strong analytical and problem-solving skills, with a data-driven approach to decision-making.

Excellent communication and interpersonal skills, capable of engaging effectively with all levels of staff and clients.

Familiarity with quality management frameworks (e.g., Six Sigma, ISO, CMMI) and quality assurance tools.

Fluency in Both Arabic and English.

Job Id: gd1+pPW/FOqHnNWrx+/UALUIK8OstEIedPtPKLYmnYl+AVUln6RIiDYG6VgLhaKOu4AY5hxNB3q0soulqExugteb6fByEXBQ+JH+XlE/zJS4GqpabqDo3YFcmFa4qiEzPFV+XTvrPGUgmF2XutKEiYF9Xr9

• Seniority level Mid-Senior level

• Employment type Full-time

• Job function Quality Assurance
• Industries Wholesale Building Materials

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• Develop, implement, and manage the company's Quality Assurance program, ensuring compliance with cGMP, ICH, and other relevant regulatory standards.
• Oversee the QMS, including SOPs, batch record review, deviation management, CAPA, change control, and complaint handling.
• Conduct internal audits and participate in external audits by regulatory agencies and customers.
• Ensure all pharmaceutical products meet defined quality standards and specifications.
• Manage the validation activities for manufacturing processes, equipment, and analytical methods.
• Review and approve batch release documentation.
• Investigate product quality issues, deviations, and out-of-specification (OOS) results, and implement corrective and preventive actions (CAPA).
• Train and mentor QA personnel and other staff on quality systems and GMP compliance.
• Liaise with regulatory authorities during inspections and submissions.
• Stay informed about new regulations, guidelines, and industry trends affecting pharmaceutical quality.
• Manage supplier qualification and auditing processes.
• Contribute to the continuous improvement of manufacturing and quality processes.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 8-10 years of experience in Quality Assurance within the pharmaceutical industry.
• Strong knowledge of Good Manufacturing Practices (GMP), regulatory requirements (FDA, EMA, SFDA), and quality systems.
• Experience with pharmaceutical product development, manufacturing, and analytical testing.
• Proven experience in conducting and managing audits, investigations, and CAPA systems.
• Excellent leadership, communication, and interpersonal skills.
• Proficiency in quality management software and tools.
• Detail-oriented with strong analytical and problem-solving abilities.
• Ability to manage multiple projects and priorities effectively.

• Lead and manage the Pharmaceutical Quality Assurance department.
• Develop, implement, and maintain the Quality Management System (QMS).
• Ensure compliance with GMP, GLP, and other relevant regulatory guidelines.
• Oversee quality control activities for raw materials, in-process samples, and finished products.
• Manage SOPs, change control, deviations, and CAPA processes.
• Conduct internal audits and support external regulatory inspections.
• Review and approve batch records, validation protocols, and reports.
• Provide training on quality systems and regulatory compliance.
• Identify and implement quality improvement initiatives.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
• Extensive knowledge of GMP, GLP, ICH guidelines, and regulatory affairs.
• Proven experience in managing QA operations and personnel.
• Strong understanding of pharmaceutical manufacturing processes and product development.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional leadership, communication, and interpersonal abilities.
• Experience with regulatory agency inspections (FDA, EMA) is essential.