212 Quality Specialist jobs in Bahrain
Quality control specialist
Manama, Capital
Vamsystems
Posted 8 days ago
Job Viewed
Job Description
- Develop organizational structures, policies, procedures and administrative systems.
- Manage and direct daily production regarding the resorts and Quality Assurance Program.
- Implement new standards which will enhance the quality standards of Resorts.
- Supervise and prepare high quality standards and consistent results.
- Coordinate with the relevant department manager to fix the noted deficiency.
- Track and follow-up with departments to ensure needed corrections have been completed in a timely manner.
- Report to the GM on the results of routine checkups, corrections and any quality control issue that may arise.
Arabic - Native / Mother Tongue
English - Fluent / Excellent
Own a Car: Any
Have Driving License: Any
- Bachelor degree
- Min 8 years of experience at the same position with reputable organizations performing the same duties.
- Fluency in Arabic & English.
- The ideal applicant must be flexible and able to handle multiple priorities, with the ability to adjust to high pressure and rapidly changing business conditions.
- Arab Nationalities preferable who has previous experience in Saudi Arabia.
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0
Pharmaceutical Quality Assurance Specialist
20150 Tubli
BHD4800 Monthly
WhatJobs
Posted today
Job Viewed
Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist to join their fully remote Quality Assurance department. This role is essential for ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy in compliance with global regulatory requirements. You will be responsible for developing, implementing, and maintaining quality management systems, conducting internal and external audits, reviewing batch records, investigating deviations and CAPAs (Corrective and Preventive Actions), and participating in regulatory inspections. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field, coupled with at least 5 years of progressive experience in pharmaceutical quality assurance. A deep understanding of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant international regulatory guidelines (e.g., FDA, EMA) is mandatory. Proven experience with quality control testing, validation processes, and risk management is highly desirable. Excellent analytical, problem-solving, and documentation skills are critical for success in this role. Strong communication and interpersonal skills are essential for collaborating effectively with cross-functional teams, including R&D, manufacturing, and regulatory affairs, in a remote setting. You will play a crucial role in upholding Our client's commitment to product quality and patient safety. This is an opportunity to contribute to a vital aspect of the pharmaceutical industry from the comfort of your home office. We are looking for individuals dedicated to excellence and continuous improvement in quality assurance.
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1
Pharmaceutical Quality Assurance Specialist
112 Bilad Al Qadeem, Capital
BHD70000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client is seeking a meticulous and detail-oriented Pharmaceutical Quality Assurance Specialist to join their team in **Tubli, Capital, BH**. This role is crucial for ensuring that all pharmaceutical products meet rigorous quality standards and comply with regulatory requirements. You will be responsible for developing, implementing, and maintaining quality assurance systems and procedures throughout the manufacturing process. The ideal candidate will have a strong background in pharmaceutical quality control, GMP (Good Manufacturing Practices), and regulatory affairs. Responsibilities include reviewing and approving batch records, validating manufacturing processes and equipment, and conducting internal audits to identify areas for improvement. You will also participate in external audits by regulatory agencies and customers, ensuring readiness and compliance. Investigating deviations, CAPAs (Corrective and Preventive Actions), and customer complaints, and implementing necessary corrective measures are key functions. This position requires a thorough understanding of pharmaceutical manufacturing, analytical testing, and documentation practices. Collaboration with various departments, including production, R&D, and regulatory affairs, is essential. The role involves developing and delivering training programs on quality systems and GMP principles to relevant personnel. You will also be involved in risk management activities related to product quality and manufacturing processes. A commitment to maintaining the highest standards of product quality and patient safety is paramount. This is an excellent opportunity to contribute to a leading pharmaceutical company and ensure the integrity of life-saving medications.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and maintain Quality Assurance systems in accordance with GMP and regulatory guidelines.
- Review and approve batch manufacturing records, analytical data, and validation reports.
- Conduct internal audits of manufacturing processes, quality control procedures, and documentation.
- Participate in external audits by regulatory authorities and customers.
- Investigate deviations, non-conformances, and customer complaints, and implement CAPAs.
- Oversee process and equipment validation activities.
- Ensure compliance with all relevant pharmaceutical regulations and standards.
- Develop and deliver training on GMP, quality systems, and related topics.
- Collaborate with cross-functional teams to resolve quality issues and improve processes.
- Manage and maintain quality-related documentation.
- Contribute to risk management activities and quality improvement initiatives.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 4 years of experience in Quality Assurance within the pharmaceutical industry.
- Strong knowledge of Good Manufacturing Practices (GMP) and relevant regulatory requirements (e.g., FDA, EMA).
- Experience with batch record review, process validation, and deviation management.
- Proficiency in quality management systems and documentation.
- Excellent analytical, problem-solving, and decision-making skills.
- Strong attention to detail and organizational abilities.
- Effective communication and interpersonal skills.
- Ability to work independently and as part of a team.
- Experience with audits and regulatory inspections.
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2
Pharmaceutical Quality Assurance Specialist
150 Ghuraifa, Capital
BHD80000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a diligent and experienced Pharmaceutical Quality Assurance Specialist to join their growing team. This role is critical for ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements. You will be responsible for developing, implementing, and maintaining quality management systems, conducting internal audits, and overseeing the investigation of deviations and CAPAs (Corrective and Preventive Actions). The ideal candidate will have a strong understanding of Good Manufacturing Practices (GMP), regulatory guidelines (FDA, EMA, etc.), and quality control principles within the pharmaceutical industry. Excellent analytical skills, meticulous attention to detail, and strong documentation abilities are essential. You will collaborate with various departments, including production, R&D, and regulatory affairs, to uphold the highest standards of product quality and safety. Responsibilities include reviewing and approving batch records, managing quality documentation, performing risk assessments, participating in regulatory inspections, leading investigations into product quality issues, implementing continuous improvement initiatives, and ensuring compliance with all relevant pharmaceutical regulations. This position is based at our facility in Jidhafs, Capital, BH . A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field is required. A minimum of 4 years of experience in pharmaceutical quality assurance or quality control is mandatory. Strong knowledge of pharmaceutical manufacturing processes and quality systems is essential. If you are a highly organized and quality-focused professional dedicated to ensuring the integrity of pharmaceutical products, we invite you to apply and contribute to our mission of delivering safe and effective medicines.
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3
Pharmaceutical Quality Assurance Specialist
BH-608 Southern, Southern
BHD85000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company committed to developing and manufacturing life-changing medicines, is seeking a meticulous and detail-oriented Pharmaceutical Quality Assurance Specialist. This role is integral to ensuring that all products meet the highest standards of quality, safety, and efficacy, in compliance with regulatory requirements. You will be responsible for reviewing and approving batch records, managing deviations and CAPAs, participating in audits, and contributing to the continuous improvement of our quality management system. The ideal candidate possesses a strong understanding of GMP guidelines and pharmaceutical manufacturing processes.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Review and approve batch production and control records.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints.
- Develop, implement, and manage Corrective and Preventive Actions (CAPA).
- Participate in internal and external audits (regulatory, customer, and supplier audits).
- Ensure compliance with current Good Manufacturing Practices (cGMP) and other relevant regulations.
- Develop, review, and approve Quality Assurance SOPs and documentation.
- Conduct quality risk assessments and implement appropriate mitigation strategies.
- Monitor and analyze quality data to identify trends and areas for improvement.
- Train personnel on quality systems and GMP requirements.
- Contribute to validation activities, including process, cleaning, and equipment validation.
- Release finished products upon confirmation of compliance with all quality standards.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, Chemical Engineering, or a related life science field.
- Minimum of 4 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of cGMP regulations (e.g., FDA, EMA).
- Experience with quality management systems, including deviation management, CAPA, change control, and audits.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and accuracy.
- Effective written and verbal communication skills.
- Ability to work collaboratively in a team environment and manage multiple tasks.
- Proficiency in Microsoft Office Suite and quality management software.
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4
Pharmaceutical Quality Assurance Specialist
222, BH Al Daih, Northern
BHD72000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client is seeking a meticulous and experienced Pharmaceutical Quality Assurance Specialist to ensure compliance with regulatory standards and internal quality systems. This critical role contributes to the integrity and safety of pharmaceutical products by overseeing and improving quality processes. The ideal candidate will possess a strong background in pharmaceutical manufacturing, quality control, and regulatory affairs, with a thorough understanding of Good Manufacturing Practices (GMP) and other relevant guidelines. You will be responsible for developing, implementing, and maintaining the Quality Management System (QMS), including SOPs, batch record reviews, deviation investigations, and change control processes. Conducting internal audits, supplier audits, and supporting regulatory inspections are key functions. You will also play a vital role in risk assessment and management, identifying potential quality issues and implementing corrective and preventive actions (CAPA). The ability to analyze quality data, generate reports, and recommend process improvements is essential. Collaboration with various departments, including production, R&D, and regulatory affairs, is crucial for ensuring a holistic approach to quality. This position offers an exciting opportunity to contribute to the development and manufacturing of high-quality pharmaceuticals in the Budaiya, Northern, BH area. This role operates on a hybrid schedule, offering a combination of on-site responsibilities and remote work flexibility.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain the Quality Management System (QMS).
- Ensure compliance with cGMP, ICH, and other relevant pharmaceutical regulations.
- Conduct internal audits and support external regulatory inspections.
- Review and approve batch records, specifications, and validation protocols.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints.
- Implement and manage Corrective and Preventive Actions (CAPA).
- Manage the change control process.
- Perform risk assessments and implement mitigation strategies.
- Develop and deliver quality-related training to personnel.
- Monitor and analyze quality metrics and trends.
- Author and review Standard Operating Procedures (SOPs).
- Collaborate with cross-functional teams on quality initiatives.
- Qualify and audit suppliers and contract manufacturers.
- Contribute to continuous improvement efforts in quality systems.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 4 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of cGMP regulations and pharmaceutical quality systems.
- Experience with audits, investigations, and validation processes.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication abilities.
- Proficiency in quality management software and tools.
- Ability to work independently and as part of a team.
- Detail-oriented with a strong commitment to quality and compliance.
- Familiarity with hybrid work environments.
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5
Pharmaceutical Quality Assurance Specialist
222 Busaiteen, Muharraq
BHD68000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a respected pharmaceutical manufacturer, is seeking a meticulous and detail-oriented Pharmaceutical Quality Assurance Specialist to join their team in Busaiteen, Muharraq, BH . This role is vital in ensuring that all pharmaceutical products manufactured meet the highest standards of quality, safety, and efficacy, adhering strictly to regulatory requirements and internal quality systems.
As a Quality Assurance Specialist, you will play a crucial role in maintaining and improving the company's Quality Management System (QMS). Your responsibilities will include reviewing and approving batch records, ensuring compliance with Good Manufacturing Practices (GMP), and participating in internal and external audits. You will conduct investigations into deviations and out-of-specification (OOS) results, identifying root causes and recommending corrective and preventive actions (CAPAs). Your work will involve the review and approval of validation protocols and reports for manufacturing processes and equipment. You will also be responsible for managing change controls, ensuring that any proposed changes are adequately assessed for their impact on product quality. Furthermore, you will contribute to the development and delivery of quality training programs for manufacturing personnel and ensure that all quality-related documentation is maintained accurately and efficiently.
Key responsibilities:
The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry is required. You must have a strong understanding of cGMP regulations, QMS principles, and pharmaceutical manufacturing processes. Excellent attention to detail, strong analytical and problem-solving skills, and proficient documentation abilities are essential. Experience with validation, change control, and deviation investigations is necessary. Good written and verbal communication skills are required to effectively interact with various departments and regulatory bodies. Familiarity with Quality by Design (QbD) principles is a plus. This is an excellent opportunity to contribute to the quality and integrity of life-saving medications.
As a Quality Assurance Specialist, you will play a crucial role in maintaining and improving the company's Quality Management System (QMS). Your responsibilities will include reviewing and approving batch records, ensuring compliance with Good Manufacturing Practices (GMP), and participating in internal and external audits. You will conduct investigations into deviations and out-of-specification (OOS) results, identifying root causes and recommending corrective and preventive actions (CAPAs). Your work will involve the review and approval of validation protocols and reports for manufacturing processes and equipment. You will also be responsible for managing change controls, ensuring that any proposed changes are adequately assessed for their impact on product quality. Furthermore, you will contribute to the development and delivery of quality training programs for manufacturing personnel and ensure that all quality-related documentation is maintained accurately and efficiently.
Key responsibilities:
- Review and approve batch manufacturing records for product release.
- Ensure compliance with current Good Manufacturing Practices (cGMP).
- Participate in and support internal and external audits (regulatory and customer).
- Investigate deviations, out-of-specification (OOS) results, and customer complaints.
- Develop, implement, and track Corrective and Preventive Actions (CAPAs).
- Review and approve validation documentation (IQ, OQ, PQ) for equipment and processes.
- Manage the change control process for manufacturing operations.
- Assist in the development and maintenance of Standard Operating Procedures (SOPs).
- Conduct quality risk assessments and implement mitigation strategies.
- Provide training on quality systems and GMP to site personnel.
The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 3 years of experience in Quality Assurance within the pharmaceutical industry is required. You must have a strong understanding of cGMP regulations, QMS principles, and pharmaceutical manufacturing processes. Excellent attention to detail, strong analytical and problem-solving skills, and proficient documentation abilities are essential. Experience with validation, change control, and deviation investigations is necessary. Good written and verbal communication skills are required to effectively interact with various departments and regulatory bodies. Familiarity with Quality by Design (QbD) principles is a plus. This is an excellent opportunity to contribute to the quality and integrity of life-saving medications.
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6
Process Improvement Engineer
1013 Tubli
BHD70000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leader in the industrial manufacturing sector, is seeking a dedicated Process Improvement Engineer to enhance operational efficiency and productivity at their facility in A'ali, Northern, Bahrain . This role is central to identifying, analyzing, and implementing improvements across various production and operational processes. The successful candidate will utilize Lean Manufacturing, Six Sigma, and other continuous improvement methodologies to streamline workflows, reduce waste, and optimize resource utilization. Responsibilities include conducting detailed process audits, data analysis, and developing strategies for enhanced performance. You will work closely with production teams, quality control, and management to implement changes, provide training, and ensure sustainable results. The role demands a strong analytical mindset, excellent problem-solving skills, and the ability to drive change in a manufacturing environment. Key performance indicators will include improvements in cycle times, defect reduction, cost savings, and overall operational output. This is a hands-on role requiring engagement on the shop floor as well as strategic planning. Join our client to contribute to operational excellence and innovation within a challenging and rewarding industrial setting.
Key Responsibilities:
Key Responsibilities:
- Analyze existing industrial processes to identify areas for improvement.
- Develop and implement process optimization strategies using Lean and Six Sigma principles.
- Conduct data analysis to measure process performance and identify root causes of issues.
- Design and implement new workflows and standard operating procedures.
- Collaborate with cross-functional teams to execute improvement initiatives.
- Train employees on new processes and methodologies.
- Monitor and report on the impact of process changes.
- Reduce waste, improve efficiency, and lower operational costs.
- Lead Kaizen events and continuous improvement projects.
- Ensure compliance with safety and quality standards.
- Bachelor's degree in Industrial Engineering, Mechanical Engineering, or a related field.
- Minimum of 4 years of experience in process improvement or industrial engineering.
- Certification in Lean Manufacturing or Six Sigma (Green Belt required, Black Belt preferred).
- Proficiency in data analysis and statistical software (e.g., Minitab).
- Strong understanding of manufacturing operations and supply chain dynamics.
- Excellent problem-solving, analytical, and project management skills.
- Effective communication and interpersonal skills to drive change.
This advertiser has chosen not to accept applicants from your region.
7
Process Improvement Engineer
310 Galali
BHD7200 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leader in the manufacturing sector, is seeking an innovative Industrial Engineering specialist for their facility in Sanad, Capital, BH . The Process Improvement Engineer will be responsible for analyzing existing production processes, identifying inefficiencies, and implementing solutions to optimize workflow, reduce waste, and enhance overall productivity. This role requires a strong analytical mindset, excellent problem-solving skills, and a deep understanding of industrial engineering principles and methodologies such as Lean Manufacturing and Six Sigma. Key responsibilities include designing and implementing new production systems, developing performance metrics, conducting time and motion studies, collaborating with production teams to implement changes, and monitoring the effectiveness of improvement initiatives. You will also be involved in evaluating new technologies and equipment to enhance operational capabilities. A Bachelor's degree in Industrial Engineering or a closely related field is required, with a Master's degree being an advantage. Proven experience in process optimization, project management, and data analysis is essential. Familiarity with CAD software and simulation tools is preferred. The role involves a hybrid work model, allowing for collaboration with teams on-site and focused analytical work remotely. Excellent communication and interpersonal skills are necessary to effectively influence change and build consensus across departments. We are looking for a driven individual passionate about driving operational excellence and contributing to sustainable growth.
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8
Process Improvement Engineer
101 Manama, Capital
BHD7000 Monthly
WhatJobs
Posted today
Job Viewed
Job Description
Our client is looking for a dedicated and analytical Process Improvement Engineer to join their operations team in **Manama, Capital, BH**. This is an on-site role focused on optimizing manufacturing and operational processes to enhance efficiency, reduce costs, and improve product quality. You will be responsible for identifying areas of inefficiency, developing data-driven solutions, and implementing process changes. This includes conducting time studies, analyzing workflows, and mapping current processes to identify bottlenecks and areas for improvement. You will work closely with production staff, management, and cross-functional teams to understand challenges and propose effective solutions.
The ideal candidate will possess a strong background in industrial engineering principles, Lean Manufacturing, Six Sigma methodologies, or other relevant process improvement frameworks. Proficiency in data analysis tools and techniques is essential, along with the ability to interpret complex data sets and translate them into actionable insights. Excellent problem-solving skills, strong communication abilities, and a collaborative approach are critical for this position. You should be comfortable presenting findings and recommendations to various levels of management. Experience with process simulation software and a good understanding of quality management systems would be a significant advantage. This role offers a fantastic opportunity to make a tangible impact on the company's performance, driving operational excellence and contributing to long-term success within a well-established organization. Your expertise will be key in streamlining operations and fostering a culture of continuous improvement.
Key Responsibilities:
The ideal candidate will possess a strong background in industrial engineering principles, Lean Manufacturing, Six Sigma methodologies, or other relevant process improvement frameworks. Proficiency in data analysis tools and techniques is essential, along with the ability to interpret complex data sets and translate them into actionable insights. Excellent problem-solving skills, strong communication abilities, and a collaborative approach are critical for this position. You should be comfortable presenting findings and recommendations to various levels of management. Experience with process simulation software and a good understanding of quality management systems would be a significant advantage. This role offers a fantastic opportunity to make a tangible impact on the company's performance, driving operational excellence and contributing to long-term success within a well-established organization. Your expertise will be key in streamlining operations and fostering a culture of continuous improvement.
Key Responsibilities:
- Analyze existing operational processes to identify inefficiencies.
- Develop and implement strategies for process optimization and cost reduction.
- Utilize Lean and Six Sigma methodologies to drive improvements.
- Collect and analyze data to measure process performance.
- Develop and maintain process documentation and standard operating procedures.
- Collaborate with production teams to implement changes and ensure adoption.
- Monitor and evaluate the effectiveness of implemented improvements.
- Train staff on new processes and best practices.
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9