135 Validation 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).
• Conduct internal audits and inspections of manufacturing processes and facilities.
• Review and approve batch manufacturing records, ensuring compliance with specifications.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, and recommend corrective and preventive actions (CAPA).
• Manage the CAPA system and ensure timely closure of all actions.
• Participate in regulatory inspections and customer audits.
• Prepare and review validation protocols and reports for equipment, processes, and analytical methods.
• Ensure compliance with relevant pharmaceutical regulations and guidelines (e.g., GMP, FDA, EMA).
• Train personnel on quality assurance procedures and GMP requirements.
• Contribute to continuous improvement initiatives within the quality department.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
• Minimum of 4 years of experience in Quality Assurance within the pharmaceutical industry.
• Thorough understanding of Good Manufacturing Practice (GMP) and regulatory requirements.
• Experience with QMS, auditing, deviation management, and CAPA systems.
• Excellent analytical, problem-solving, and documentation skills.
• Strong attention to detail and accuracy.
• Proficiency in Microsoft Office Suite and familiarity with quality-related software.
• Excellent written and verbal communication skills.
• Ability to work independently and collaboratively in a team environment in Hidd, Muharraq, BH .

• Develop, implement, and manage the company's Quality Management System (QMS) in accordance with relevant industry standards (e.g., ISO 9001).
• Establish and maintain quality control procedures and protocols for all stages of the manufacturing process, from raw material inspection to finished product release.
• Lead and mentor the QA team, fostering a culture of quality consciousness and continuous improvement.
• Conduct regular internal audits and inspections to ensure compliance with QMS requirements and identify areas for enhancement.
• Oversee the investigation of quality deviations, customer complaints, and non-conformances, implementing effective corrective and preventive actions (CAPA).
• Analyze quality data, identify trends, and prepare comprehensive reports for senior management.
• Collaborate with production, engineering, and R&D departments to address quality issues and implement process improvements.
• Manage supplier quality, including the qualification of new suppliers and the monitoring of their performance.
• Ensure that all products meet defined quality specifications and regulatory requirements.
• Stay updated on industry best practices, regulatory changes, and emerging quality control technologies.
• Manage the calibration and maintenance program for all quality control equipment.
• Develop and deliver quality training programs for employees across various departments.

• Bachelor's degree in Engineering, Science, or a related technical field. A Master's degree or relevant professional certification (e.g., ASQ Certified Quality Manager) is highly desirable.
• A minimum of 7 years of experience in Quality Assurance or Quality Control within a manufacturing environment.
• Proven track record of successfully implementing and managing QMS, preferably ISO 9001 certified.
• Strong knowledge of statistical quality control techniques, root cause analysis, and CAPA implementation.
• Experience with auditing (internal and external) and supplier quality management.
• Excellent leadership, team management, and communication skills.
• Proficiency in data analysis and reporting tools.
• Demonstrated ability to drive continuous improvement initiatives.
• Familiarity with manufacturing processes relevant to the industry.
• Strong problem-solving and decision-making capabilities.

• Ensure compliance with GMP, GDP, and other relevant pharmaceutical regulations.
• Develop, implement, and maintain the Quality Management System (QMS).
• Conduct internal audits and participate in external regulatory inspections.
• Review and approve batch manufacturing and packaging records.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints.
• Manage change control processes and ensure proper documentation.
• Participate in the validation of processes, equipment, and analytical methods.
• Ensure all quality-related documentation is accurate, complete, and maintained.
• Collaborate with cross-functional teams to address quality issues.
• Prepare and present quality metrics and reports to management.

• Develop, implement, and maintain comprehensive quality management systems (QMS) in alignment with ISO standards.
• Establish and monitor key performance indicators (KPIs) for quality control processes.
• Lead and mentor the QA team, providing training, performance feedback, and development opportunities.
• Conduct regular audits of manufacturing processes to ensure compliance with quality protocols and identify areas for improvement.
• Investigate product defects and customer complaints, determining root causes and implementing corrective and preventive actions (CAPA).
• Collaborate with R&D and production teams to ensure new products meet quality specifications before market release.
• Manage the inspection and testing of raw materials, in-process goods, and finished products.
• Oversee calibration and maintenance of quality control equipment.
• Prepare detailed quality reports for management, highlighting trends, issues, and improvement plans.
• Ensure all operations comply with relevant industry regulations and certifications.
• Drive initiatives to reduce waste, scrap, and rework through quality improvement programs.
• Facilitate cross-functional team meetings to address quality-related challenges.
• Maintain accurate records and documentation related to quality control activities.
• Champion a culture of quality throughout the organization.
• Stay updated on industry best practices and emerging quality assurance technologies.
• Implement statistical process control (SPC) methodologies.
• Manage supplier quality assurance programs.
• Develop and execute quality training programs for all manufacturing personnel.

• Bachelor's degree in Engineering, Manufacturing Technology, or a related discipline.
• Proven experience (5+ years) in a quality assurance or quality control role within a manufacturing environment.
• Demonstrated leadership experience managing a QA team.
• Strong knowledge of quality management systems (e.g., ISO 9001, Six Sigma).
• Expertise in quality control tools and methodologies, including SPC, FMEA, and root cause analysis.
• Excellent analytical, problem-solving, and decision-making skills.
• Proficiency in data analysis and reporting.
• Strong communication and interpersonal skills, with the ability to collaborate effectively across departments.
• Experience in the specific manufacturing sector of our client is highly preferred.