1 355 Quality Manager jobs in Bahrain
Quality Manager
Posted today
Job Viewed
Job Description
Overview
*** This position is contingent upon contract award ***
SOS International LLC is seeking a Quality Manager for a $50 million/year operation and maintenance (O&M) and life support services (LSS) contract in the Middle East.
The Quality Manager is responsible for developing, implementing, and maintaining a comprehensive Quality Management System (QMS) to ensure consistent delivery of high-quality O&M and LSS across three geographically dispersed sites. This role ensures compliance with contract requirements, international standards, and client expectations, while driving continuous improvement and risk mitigation.
Essential Job Duties
- Develop, implement, and maintain a QMS aligned with ISO 9001 and other applicable standards.
- Ensure quality policies, procedures, and plans are effectively communicated and followed across all operating locations.
- Conduct regular reviews and updates of the QMS to reflect operational changes and lessons learned.
- Plan and execute internal audits, site inspections, and quality reviews across all three locations.
- Coordinate and support external audits by clients or regulatory bodies.
- Track and close out audit findings, non-conformances, and corrective/preventive actions (CAPAs).
- Define and monitor Key Performance Indicators (KPIs) and Service Level Agreements (SLAs).
- Analyze trends and performance data to identify areas for improvement.
- Prepare and present quality reports to senior leadership and clients.
- Develop and deliver quality training programs for staff and subcontractors.
- Promote a culture of quality, safety, and continuous improvement throughout the organization.
- Identify quality-related risks and implement mitigation strategies.
- Ensure compliance with contractual, regulatory, and industry standards.
- Support incident investigations and root cause analyses.
- Serve as the primary point of contact for all quality-related matters.
- Collaborate with site managers, operations teams, and client representatives to resolve quality issues.
- Provide input into proposals, contract modifications, and process improvements.
Minimum Requirements
- Bachelor's degree in Quality Management, Engineering, Facilities Management, or a related field.
- Minimum five (5) years of experience in quality management for large-scale O&M or LSS contracts.
- Experience working in the Middle East or in austere environments is highly desirable.
- Strong knowledge of ISO 9001 and other relevant quality standards.
- Excellent analytical, communication, and leadership skills.
Familiarity with U.S. Government contracting requirements is a plus.
Preferred Qualifications
- Certified Quality Auditor (CQA), Six Sigma, or similar certifications preferred.
Work Environment
- Frequent travel between program operating locations.
- Must be able to work in austere environments and adapt to cultural and operational nuances.
Working at SOSi
All interested individuals will receive consideration and will not be discriminated against for any reason.
Quality Manager (OCONUS)
Posted 6 days ago
Job Viewed
Job Description
*** This position is contingent upon contract award ***
SOS International LLC is seeking a Quality Manager for a $50 million/year operation and maintenance (O&M) and life support services (LSS) contract in the Middle East.
The Quality Manager is responsible for developing, implementing, and maintaining a comprehensive Quality Management System (QMS) to ensure consistent delivery of high-quality O&M and LSS across three geographically dispersed sites. This role ensures compliance with contract requirements, international standards, and client expectations, while driving continuous improvement and risk mitigation.
**Essential Job Duties**
+ Develop, implement, and maintain a QMS aligned with ISO 9001 and other applicable standards.
+ Ensure quality policies, procedures, and plans are effectively communicated and followed across all operating locations.
+ Conduct regular reviews and updates of the QMS to reflect operational changes and lessons learned.
+ Plan and execute internal audits, site inspections, and quality reviews across all three locations.
+ Coordinate and support external audits by clients or regulatory bodies.
+ Track and close out audit findings, non-conformances, and corrective/preventive actions (CAPAs).
+ Define and monitor Key Performance Indicators (KPIs) and Service Level Agreements (SLAs).
+ Analyze trends and performance data to identify areas for improvement.
+ Prepare and present quality reports to senior leadership and clients.
+ Develop and deliver quality training programs for staff and subcontractors.
+ Promote a culture of quality, safety, and continuous improvement throughout the organization.
+ Identify quality-related risks and implement mitigation strategies.
+ Ensure compliance with contractual, regulatory, and industry standards.
+ Support incident investigations and root cause analyses.
+ Serve as the primary point of contact for all quality-related matters.
+ Collaborate with site managers, operations teams, and client representatives to resolve quality issues.
+ Provide input into proposals, contract modifications, and process improvements.
**Minimum Requirements**
+ Bachelor's degree in Quality Management, Engineering, Facilities Management, or a related field.
+ Minimum five (5) years of experience in quality management for large-scale O&M or LSS contracts.
+ Experience working in the Middle East or in austere environments is highly desirable.
+ Strong knowledge of ISO 9001 and other relevant quality standards.
+ Excellent analytical, communication, and leadership skills.
+ Familiarity with U.S. Government contracting requirements is a plus.
**Preferred Qualifications**
+ Certified Quality Auditor (CQA), Six Sigma, or similar certifications preferred.
**Work Environment**
+ Frequent travel between program operating locations.
+ Must be able to work in austere environments and adapt to cultural and operational nuances.
**Working at SOSi**
All interested individuals will receive consideration and will not be discriminated against for any reason.
SOSi is an equal employment opportunity employer and affirmative action employer. All interested individuals will receive consideration and will not be discriminated against on the basis of race, color, religion, sex, national origin, disability, age, sexual orientation, gender identity, genetic information, or protected veteran status. SOSi takes affirmative action in support of its policy to advance diversity and inclusion of individuals who are minorities, women, protected veterans, and individuals with disabilities.
Production Quality Manager
Posted 25 days ago
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Job Description
Key responsibilities include developing and implementing quality control procedures, conducting regular inspections and audits of production lines, and analyzing quality data to identify areas for improvement. You will manage the disposition of non-conforming materials and products, work with production teams to implement corrective and preventive actions, and ensure compliance with relevant industry standards and certifications. The ideal candidate will possess a strong understanding of manufacturing processes, quality management systems (e.g., ISO 9001), and statistical process control techniques. Excellent leadership, problem-solving, and communication skills are paramount. A Bachelor's degree in Engineering, Manufacturing Technology, or a related field is required. A minimum of 7 years of experience in quality assurance or quality control within a manufacturing environment is necessary. Experience in managing a quality team is highly desirable. You should be adept at fostering a collaborative environment and driving continuous improvement initiatives. This role requires a hands-on approach and a commitment to upholding the highest standards of product quality. The Production Quality Manager will be instrumental in safeguarding our reputation for delivering reliable and high-performance products.
Quality Assurance Manager
Posted 8 days ago
Job Viewed
Job Description
Key responsibilities include:
- Developing and implementing comprehensive quality assurance strategies and plans for all manufacturing processes.
- Establishing and enforcing quality control standards, procedures, and testing protocols.
- Leading, mentoring, and managing the QA team, including training and performance evaluation.
- Conducting regular audits of manufacturing processes and finished products to ensure compliance with quality standards.
- Investigating quality deviations, customer complaints, and non-conformance issues, identifying root causes, and implementing corrective and preventive actions (CAPA).
- Collaborating with production, R&D, and engineering teams to ensure product quality is integrated throughout the product lifecycle.
- Managing all documentation related to quality control, including specifications, test methods, and batch records.
- Ensuring compliance with relevant industry regulations and certifications (e.g., ISO).
- Analyzing quality data to identify trends, inefficiencies, and areas for improvement.
- Promoting a culture of quality awareness and continuous improvement throughout the organization.
The ideal candidate will possess a Bachelor's degree in Engineering (Mechanical, Chemical, or Industrial) or a related scientific field. A Master's degree is a plus. A minimum of 7 years of experience in quality assurance within a manufacturing environment is required, with at least 3 years in a management or supervisory role. Proven experience with quality management systems (QMS), such as ISO 9001, and familiarity with Lean manufacturing principles are essential. Strong knowledge of statistical process control (SPC) and various quality tools is mandatory. Excellent leadership, problem-solving, analytical, and communication skills are critical. This role requires the candidate to be present at the **Saar, Northern, BH** facility.
Quality Assurance Manager
Posted 25 days ago
Job Viewed
Job Description
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Oversee all quality assurance and quality control activities throughout the manufacturing process.
- Establish and monitor quality metrics and KPIs, analyzing data to identify trends and areas for improvement.
- Conduct regular internal audits and inspections to ensure compliance with quality standards and procedures.
- Lead and manage the QA team, providing training, guidance, and performance feedback.
- Investigate product quality issues, root cause analysis, and implement corrective and preventive actions (CAPA).
- Collaborate with production, engineering, and R&D teams to ensure product quality from design to launch.
- Ensure compliance with relevant industry regulations and certifications (e.g., ISO 9001).
- Manage supplier quality by assessing and auditing suppliers' quality systems.
- Prepare quality reports for senior management, highlighting performance, issues, and improvement initiatives.
- Drive a culture of quality throughout the organization.
- Bachelor's degree in Engineering, Science, or a related field.
- Minimum of 6 years of experience in Quality Assurance or Quality Control, with at least 3 years in a management role within manufacturing.
- In-depth knowledge of Quality Management Systems (QMS), ISO 9001, and relevant manufacturing quality standards.
- Strong understanding of statistical process control (SPC) and root cause analysis methodologies.
- Experience with quality auditing and regulatory compliance.
- Excellent leadership, team management, and problem-solving skills.
- Proficiency in quality management software and tools.
- Strong analytical and reporting skills.
- Excellent communication and interpersonal skills.
Quality Assurance Manager
Posted 25 days ago
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Job Description
Responsibilities:
- Develop, implement, and maintain the company's overall Quality Management System (QMS) in compliance with relevant standards (e.g., ISO 9001).
- Lead and mentor the Quality Assurance team, providing guidance and fostering professional development.
- Establish and monitor key quality performance indicators (KPIs) and ensure targets are met.
- Oversee the inspection and testing of raw materials, in-process products, and finished goods.
- Investigate quality deviations, customer complaints, and non-conformances, implementing effective corrective and preventive actions (CAPA).
- Conduct internal audits and facilitate external audits by certification bodies or customers.
- Collaborate with production and engineering teams to identify and address quality issues at the source.
- Manage product traceability and documentation control processes.
- Stay updated on evolving quality standards, regulations, and best practices in the manufacturing industry.
- Drive a culture of quality throughout the organization.
- Manage supplier quality assurance programs.
- Prepare quality reports for senior management.
- Bachelor's degree in Engineering, Chemistry, Science, or a related field.
- Minimum of 7 years of experience in Quality Assurance or Quality Control within a manufacturing environment.
- Proven experience in developing and implementing ISO 9001 or similar QMS.
- Strong understanding of quality control tools and methodologies (e.g., SPC, FMEA, Root Cause Analysis).
- Experience with conducting audits and managing corrective actions.
- Excellent leadership, analytical, and problem-solving skills.
- Strong attention to detail and commitment to quality.
- Effective communication and interpersonal skills, with the ability to collaborate across departments.
- Proficiency in quality management software and Microsoft Office Suite.
- Experience in the specific manufacturing sector of our client is highly desirable.
Senior Sanitation Quality Manager
Posted 1 day ago
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Job Description
Key Responsibilities:
- Develop, implement, and maintain comprehensive sanitation and hygiene programs.
- Conduct regular inspections and audits to ensure compliance with health regulations and company standards.
- Train and supervise cleaning staff, ensuring adherence to SOPs.
- Monitor and manage the inventory and proper use of cleaning supplies and equipment.
- Investigate and resolve sanitation-related complaints or issues.
- Analyze sanitation data to identify trends and areas for improvement.
- Develop and update sanitation policies and procedures as needed.
- Collaborate with other departments to ensure seamless integration of sanitation practices.
- Stay informed about industry best practices and regulatory changes in sanitation and hygiene.
- Promote a culture of cleanliness and safety throughout the organization.
- Bachelor's degree in Environmental Health, Public Health, Biology, or a related field.
- Minimum of 6 years of experience in sanitation management, quality assurance, or a related role, preferably within a commercial or industrial setting.
- Proven experience in developing and implementing sanitation programs.
- Strong knowledge of health and safety regulations, HACCP principles, and sanitation best practices.
- Excellent leadership, training, and supervisory skills.
- Proficiency in conducting audits and inspections.
- Strong analytical and problem-solving abilities.
- Effective communication and interpersonal skills.
- Ability to work independently and manage multiple priorities.
- Experience with pest control and waste management is advantageous.
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Remote Sanitation Quality Manager
Posted 5 days ago
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Job Description
The ideal candidate will have a strong background in sanitation management, quality assurance, and regulatory compliance, ideally within industries such as food service, healthcare, or hospitality. You must possess exceptional analytical skills, a keen eye for detail, and the ability to interpret complex regulations. Excellent written and verbal communication skills are essential for clear reporting, training development, and effective collaboration with diverse teams. Proficiency in data analysis tools and virtual communication platforms is a must. This role demands a proactive approach to identifying potential risks and implementing preventative measures. You will play a pivotal role in maintaining the highest standards of hygiene and safety, ensuring that all operational sites meet or exceed industry benchmarks. This is a remote-first opportunity, allowing for a flexible work schedule while maintaining robust oversight.
Responsibilities:
- Develop, implement, and monitor sanitation policies and procedures.
- Conduct remote audits and inspections of facilities to ensure compliance.
- Analyze sanitation data and reports to identify trends and areas for improvement.
- Create and deliver training programs on sanitation best practices.
- Collaborate with site managers to implement corrective action plans.
- Ensure compliance with all relevant health, safety, and environmental regulations.
- Stay updated on industry best practices and regulatory changes.
- Manage the quality assurance program for cleaning operations.
- Investigate and resolve sanitation-related complaints or issues.
- Prepare regular reports on sanitation performance and quality metrics.
- Bachelor's degree in Environmental Health, Public Health, Food Science, or a related field.
- 5+ years of experience in sanitation management, quality assurance, or a similar role.
- Proven knowledge of sanitation principles, cleaning chemicals, and equipment.
- Familiarity with relevant health and safety regulations (e.g., HACCP, OSHA).
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Proficiency in data analysis and reporting tools.
- Experience with virtual collaboration and auditing tools.
- Ability to work independently and manage multiple projects remotely.
Senior Pharmaceutical Quality Manager
Posted 19 days ago
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Job Description
In this remote position, you will be responsible for establishing, implementing, and maintaining a robust Quality Management System (QMS) across all pharmaceutical operations. This includes developing and enforcing quality policies, procedures, and standards. You will conduct internal audits, manage external audits by regulatory agencies and partners, and oversee the CAPA (Corrective and Preventive Actions) system to ensure timely and effective resolution of quality issues. A key focus will be on continuous improvement of quality processes to enhance compliance and operational excellence.
The successful applicant will have a strong ability to interpret and apply complex regulatory guidelines from authorities such as the FDA, EMA, and other relevant bodies. You will provide expert guidance on quality-related matters to cross-functional teams, including R&D, manufacturing, and supply chain. Responsibilities will include reviewing and approving critical quality documents, such as batch records, validation reports, and change controls. Leading quality risk assessments and implementing risk mitigation strategies will be essential. This role demands exceptional leadership, analytical skills, and the ability to drive a culture of quality throughout the organization, even within a dispersed team.
This is a strategic role that requires proactive engagement with senior management to report on the state of quality and compliance, and to champion quality initiatives. You will be responsible for training and mentoring quality assurance personnel, ensuring their professional development and adherence to best practices. A thorough understanding of pharmaceutical manufacturing processes and analytical testing is highly advantageous. This is a fully remote opportunity, providing significant autonomy and the chance to shape the quality landscape of our innovative pharmaceutical products.
Required Qualifications: Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline; advanced degree or relevant professional certification (e.g., ASQ CQE, CQA) strongly preferred. Minimum of 10 years of experience in pharmaceutical quality assurance and quality control, with at least 5 years in a management role. Deep understanding and practical application of GMP, ICH guidelines, and other relevant pharmaceutical regulations. Proven experience in developing, implementing, and managing comprehensive Quality Management Systems (QMS). Demonstrated success in managing internal and external audits, and leading regulatory inspections. Strong expertise in CAPA management, root cause analysis, and risk management principles. Excellent analytical, problem-solving, and decision-making skills. Outstanding communication, interpersonal, and leadership abilities. Ability to work independently and lead remote teams effectively. Thorough knowledge of pharmaceutical manufacturing operations and analytical testing is essential. This role is entirely remote, requiring strong self-management and virtual collaboration skills.
Responsibilities include:
- Developing, implementing, and maintaining the company's Quality Management System (QMS).
- Ensuring compliance with all applicable pharmaceutical regulations (e.g., GMP, ICH).
- Conducting internal audits and managing external audits and regulatory inspections.
- Overseeing the CAPA system, including investigation, root cause analysis, and corrective/preventive actions.
- Providing quality guidance and support to cross-functional teams.
- Reviewing and approving critical quality-related documents.
- Leading quality risk management activities and implementing mitigation strategies.
- Monitoring key quality metrics and driving continuous improvement initiatives.
- Training and mentoring QA/QC personnel.
- Reporting on the state of quality and compliance to senior management.
- Staying current with evolving regulatory requirements and industry best practices.
Pharmaceutical Quality Assurance Manager
Posted 1 day ago
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Job Description
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant regulatory standards.
- Oversee and manage quality control activities, including batch record review and release.
- Conduct internal audits and support external regulatory inspections (e.g., FDA, EMA).
- Manage deviations, non-conformances, and CAPA processes effectively.
- Review and approve validation protocols and reports for equipment, processes, and systems.
- Provide quality assurance support to R&D, production, and other departments.
- Train personnel on quality assurance procedures and regulatory requirements.
- Monitor key quality metrics and provide reports to senior management.
- Contribute to the continuous improvement of quality processes and systems.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5 years of experience in pharmaceutical quality assurance or quality control.
- Strong knowledge of GMP, GCP, ICH guidelines, and other relevant pharmaceutical regulations.
- Experience with QMS development, audit processes, and deviation management.
- Excellent analytical, problem-solving, and decision-making skills.
- Meticulous attention to detail and strong organizational abilities.
- Effective communication and interpersonal skills, with the ability to collaborate across departments.
- Proficiency in relevant software applications (e.g., LIMS, ERP systems).
- Experience in pharmaceutical manufacturing is highly preferred.