Explore exciting Quality Analyst job opportunities. Quality Analysts are vital in various sectors, focusing on maintaining and improving product and service standards. They conduct tests, analyze 1 015 Quality Analyst jobs in Bahrain
Senior Pharmaceutical Quality Analyst
6060 Al Jasra
BHD85000 Annually
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Our client, a leading pharmaceutical company, is seeking a highly qualified Senior Pharmaceutical Quality Analyst to join their dedicated quality assurance team in **Hidd, Muharraq, BH**. This crucial role will ensure that all manufactured pharmaceutical products meet stringent quality standards, regulatory requirements, and internal specifications. The Senior Pharmaceutical Quality Analyst will be responsible for developing, implementing, and maintaining quality control procedures and systems. Key responsibilities include conducting in-depth analysis of raw materials, in-process samples, and finished products using various analytical techniques and instrumentation. You will meticulously review and approve batch records, deviation reports, and change controls, ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, quality risk management, and analytical validation. Excellent attention to detail, strong problem-solving skills, and the ability to interpret complex data are essential. You will also be involved in internal and external audits, ensuring readiness for regulatory inspections. This position requires a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, along with significant experience in pharmaceutical quality assurance or control. Strong communication and interpersonal skills are necessary for collaborating with cross-functional teams, including production, R&D, and regulatory affairs. The ability to work independently and manage multiple priorities in a fast-paced environment is key. Join our client and contribute to the development and production of life-saving medicines.
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Senior Pharmaceutical Quality Analyst
450 Bilad Al Qadeem, Capital
BHD80000 Annually
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Our client, a leading pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Quality Analyst to join their team in Sitra, Capital, BH . This critical role will involve ensuring that all products meet rigorous quality standards and regulatory requirements throughout the manufacturing process. The successful candidate will contribute significantly to maintaining the integrity and safety of our pharmaceutical offerings. This is an on-site position.
Responsibilities:
Responsibilities:
- Conduct detailed analysis of raw materials, in-process samples, and finished products using various analytical techniques and laboratory equipment.
- Develop, validate, and implement analytical methods according to established protocols and regulatory guidelines (e.g., GMP, ICH).
- Perform stability studies and environmental monitoring to assess product quality and shelf-life.
- Investigate out-of-specification (OOS) results, deviations, and non-conformances, identifying root causes and recommending corrective and preventive actions (CAPAs).
- Maintain accurate and comprehensive laboratory records, batch records, and quality documentation.
- Prepare and review Certificates of Analysis (CoA) and other quality-related reports.
- Ensure compliance with all company policies, Standard Operating Procedures (SOPs), and Good Manufacturing Practices (GMP).
- Participate in internal and external audits and regulatory inspections.
- Collaborate with R&D, Manufacturing, and Regulatory Affairs departments to resolve quality issues.
- Stay updated on current industry trends, scientific advancements, and regulatory changes in pharmaceutical quality control.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5 years of experience in pharmaceutical quality control or quality assurance.
- Proficiency in analytical techniques such as HPLC, GC, UV-Vis spectroscopy, dissolution testing, and KF titration.
- Thorough understanding of GMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
- Experience with laboratory information management systems (LIMS) is a plus.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team in a fast-paced laboratory environment.
- Meticulous attention to detail and a commitment to accuracy.
- Experience in sterile manufacturing environments is highly desirable.
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1
Senior Pharmaceutical Quality Analyst
2025 Saar, Northern
BHD80000 Annually
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Our client, a prominent player in the pharmaceutical sector, is seeking a meticulous and experienced Senior Pharmaceutical Quality Analyst to join their team. This role is critical for ensuring the highest standards of quality and compliance are maintained throughout the drug manufacturing process. You will be responsible for performing a wide range of quality control tests on raw materials, in-process samples, and finished products using various analytical techniques. Key duties include conducting assays, identifying impurities, and verifying that all products meet stringent regulatory specifications and company standards. You will also be involved in method development and validation, as well as the preparation and review of detailed analytical reports and documentation. The Senior Pharmaceutical Quality Analyst will play a vital role in investigating deviations, out-of-specification (OOS) results, and customer complaints, working collaboratively with production and R&D teams to implement corrective and preventive actions (CAPAs). This position requires a strong foundation in analytical chemistry, spectroscopy (e.g., HPLC, GC, UV-Vis, IR), and microbiological testing methods. A Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline is mandatory, along with a minimum of 4-5 years of hands-on experience in a pharmaceutical quality control or quality assurance environment. Thorough knowledge of cGMP (current Good Manufacturing Practices), FDA regulations, and ICH guidelines is essential. Excellent data analysis skills, attention to detail, and the ability to work effectively in a fast-paced laboratory setting are required. Strong written and verbal communication skills are necessary for report generation and interdepartmental collaboration. This is an excellent opportunity to contribute to the quality assurance of life-saving medications and advance your career in pharmaceutical quality management.
Key Responsibilities:
Key Responsibilities:
- Perform quality control testing on raw materials, intermediates, and finished products.
- Utilize analytical techniques such as HPLC, GC, and spectroscopy.
- Ensure compliance with cGMP and regulatory guidelines.
- Investigate deviations and OOS results.
- Develop and validate analytical methods.
- Prepare and review analytical reports and documentation.
- Collaborate with R&D and production teams.
- Maintain laboratory equipment and calibration records.
- Contribute to quality risk assessments.
- Ensure product quality and safety.
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2
Senior Pharmaceutical Quality Analyst
44115 Busaiteen, Muharraq
BHD90000 Annually
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Our client is seeking a highly experienced Senior Pharmaceutical Quality Analyst to join their dedicated quality assurance team in **Busaiteen, Muharraq, BH**. This critical role involves ensuring the consistent quality and safety of pharmaceutical products through rigorous testing, analysis, and compliance monitoring. The ideal candidate will possess a strong background in pharmaceutical sciences, analytical chemistry, and regulatory affairs, coupled with meticulous attention to detail.
Key responsibilities include:
Qualifications:
This is a prime opportunity for a seasoned quality professional to make a significant contribution to pharmaceutical product integrity within our esteemed organization in **Busaiteen**.
Key responsibilities include:
- Performing analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, Karl Fischer titration).
- Developing, validating, and implementing analytical methods according to pharmacopeial standards (USP, EP) and regulatory guidelines (ICH).
- Analyzing and interpreting test data, preparing comprehensive reports, and documenting results in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Investigating out-of-specification (OOS) results and deviations, identifying root causes, and implementing corrective and preventive actions (CAPAs).
- Collaborating with production, R&D, and regulatory affairs departments to ensure product quality throughout the manufacturing process.
- Reviewing batch records and quality control data for completeness and accuracy.
- Participating in internal and external audits, inspections, and quality reviews.
- Maintaining laboratory equipment, ensuring calibration and proper functioning.
- Staying current with scientific advancements, regulatory changes, and industry best practices in pharmaceutical quality control.
- Contributing to the continuous improvement of quality systems and processes.
- Training junior analysts and providing technical guidance.
- Ensuring compliance with all safety procedures in the laboratory environment.
Qualifications:
- Master's or Ph.D. in Pharmacy, Pharmaceutical Sciences, Chemistry, or a related field.
- A minimum of 5 years of experience in pharmaceutical quality control or quality assurance.
- Extensive hands-on experience with analytical instrumentation commonly used in the pharmaceutical industry.
- Thorough knowledge of GMP, GLP, ICH guidelines, and pharmacopeial standards.
- Proven experience in method development and validation.
- Strong understanding of data integrity principles.
- Excellent analytical, problem-solving, and documentation skills.
- Proficiency in statistical analysis software.
- Strong communication and interpersonal skills for effective collaboration.
- Ability to manage multiple priorities and work independently in a fast-paced environment.
This is a prime opportunity for a seasoned quality professional to make a significant contribution to pharmaceutical product integrity within our esteemed organization in **Busaiteen**.
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3
Senior Pharmaceutical Quality Analyst
115 Bilad Al Qadeem, Capital
BHD75000 Annually
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Our client is seeking an experienced Senior Pharmaceutical Quality Analyst to join their fully remote, global team. This pivotal role involves ensuring the highest standards of quality across our pharmaceutical product lifecycle, from development to manufacturing. The ideal candidate will possess a strong understanding of regulatory affairs, quality management systems, and analytical testing methodologies within the pharmaceutical industry. You will play a key role in maintaining compliance with international pharmaceutical standards and driving continuous improvement in quality processes. This is a remote-first position, requiring excellent self-management and communication skills.
Responsibilities:
Qualifications:
Responsibilities:
- Develop and implement quality control procedures and protocols.
- Conduct rigorous analysis of raw materials, in-process samples, and finished products.
- Ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
- Prepare and review batch records, analytical reports, and validation documents.
- Investigate deviations, out-of-specification results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Collaborate with R&D, manufacturing, and regulatory affairs teams to resolve quality issues.
- Maintain and calibrate laboratory equipment.
- Participate in internal and external audits.
- Stay updated on pharmaceutical regulations and industry trends.
- Train and mentor junior quality control personnel.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 4 years of experience in pharmaceutical quality control or quality assurance.
- In-depth knowledge of pharmaceutical manufacturing processes and quality systems.
- Experience with analytical techniques (e.g., HPLC, GC, UV-Vis, Karl Fischer).
- Familiarity with ICH guidelines and regulatory submissions.
- Strong understanding of GMP/GLP requirements.
- Excellent analytical, problem-solving, and documentation skills.
- Ability to manage projects and work independently in a remote setting.
- Proficiency in data analysis software and LIMS.
- Strong written and verbal communication skills.
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4
Senior Pharmaceutical Quality Analyst
71640 Southern, Southern
BHD80000 Annually
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Our client, a leading pharmaceutical manufacturer, is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Analyst to join their esteemed team in Nuwaidrat, Southern, BH . This critical role will ensure that all manufactured products meet stringent quality standards and regulatory requirements. The Senior Pharmaceutical Quality Analyst will be responsible for developing, implementing, and maintaining quality control systems and procedures. Key duties include performing laboratory testing on raw materials, in-process samples, and finished products; analyzing test results; investigating deviations and out-of-specification results; and preparing comprehensive quality reports. You will also play a key role in audits, regulatory inspections, and continuous improvement initiatives. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline. A minimum of 6 years of experience in pharmaceutical quality control or quality assurance is required, with a strong understanding of cGMP guidelines and relevant regulatory frameworks (e.g., FDA, EMA). Exceptional analytical skills, meticulous attention to detail, and proficiency in analytical instrumentation and methodologies are essential. Excellent documentation, communication, and problem-solving skills are also necessary. This is an outstanding opportunity for a dedicated quality professional to contribute to the development and production of life-saving medications within a globally recognized company. We offer a competitive salary, excellent benefits, and a supportive work environment focused on scientific excellence and career growth.
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5
Remote Senior Pharmaceutical Quality Analyst
101 Zallaq, Southern
BHD7200 Annually
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Our client, a leading innovator in the pharmaceutical industry, is seeking a highly motivated and experienced Remote Senior Pharmaceutical Quality Analyst. This is a fully remote opportunity, allowing you to contribute to global health from anywhere. You will be responsible for ensuring the highest standards of quality and compliance in our pharmaceutical products and processes. This role involves in-depth analysis of product data, validation of manufacturing processes, and development of quality improvement initiatives. Your expertise will be vital in maintaining regulatory compliance and ensuring patient safety. Key responsibilities include:
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 5-7 years of experience in pharmaceutical quality assurance or quality control is required. Proven experience with GMP regulations, QMS, validation processes, and analytical techniques is essential. Excellent analytical, problem-solving, and communication skills are a must. The ability to work independently, manage projects effectively, and collaborate with diverse teams in a remote setting is critical. If you are passionate about ensuring the quality and safety of life-saving medications, we encourage you to apply.
- Developing and implementing robust quality control strategies for pharmaceutical manufacturing.
- Analyzing batch records, stability data, and other quality-related information to ensure product integrity.
- Performing risk assessments on manufacturing processes and identifying potential quality deviations.
- Validating analytical methods and ensuring their accuracy and reliability.
- Writing and reviewing Standard Operating Procedures (SOPs), batch records, and quality reports.
- Collaborating with R&D, manufacturing, and regulatory affairs teams to resolve quality issues.
- Participating in internal and external audits and ensuring compliance with GMP (Good Manufacturing Practices) and other relevant regulations.
- Investigating out-of-specification (OOS) results and implementing effective corrective and preventive actions (CAPAs).
- Managing and maintaining the company's Quality Management System (QMS).
- Staying updated on pharmaceutical industry trends, regulatory guidelines, and quality best practices.
- Mentoring junior quality analysts and providing technical guidance.
- Contributing to the continuous improvement of quality processes and product lifecycle management.
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field. A minimum of 5-7 years of experience in pharmaceutical quality assurance or quality control is required. Proven experience with GMP regulations, QMS, validation processes, and analytical techniques is essential. Excellent analytical, problem-solving, and communication skills are a must. The ability to work independently, manage projects effectively, and collaborate with diverse teams in a remote setting is critical. If you are passionate about ensuring the quality and safety of life-saving medications, we encourage you to apply.
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6
Quality Control Analyst
131 Hamad Town, Northern
BHD2800 month
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Our client, a reputable pharmaceutical company, is seeking a meticulous and experienced Quality Control Analyst to join their state-of-the-art facility in **Hamad Town, Northern, BH**. This role is integral to ensuring that all manufactured products meet stringent quality standards and regulatory requirements. The successful candidate will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment.
Key responsibilities include executing validated analytical methods, meticulously documenting all testing procedures and results, and adhering strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will be involved in instrument calibration and maintenance, troubleshooting analytical issues, and contributing to the continuous improvement of quality control processes. A strong understanding of pharmaceutical quality systems and regulatory guidelines is essential for this position. The ability to work collaboratively with production and R&D teams to resolve quality issues is also highly valued.
Key Responsibilities:
Qualifications:
This is an outstanding opportunity to join a forward-thinking pharmaceutical company in **Hamad Town, Northern, BH** and contribute to the development and manufacturing of high-quality medicines.
Key responsibilities include executing validated analytical methods, meticulously documenting all testing procedures and results, and adhering strictly to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). You will be involved in instrument calibration and maintenance, troubleshooting analytical issues, and contributing to the continuous improvement of quality control processes. A strong understanding of pharmaceutical quality systems and regulatory guidelines is essential for this position. The ability to work collaboratively with production and R&D teams to resolve quality issues is also highly valued.
Key Responsibilities:
- Perform qualitative and quantitative tests on raw materials, in-process materials, and finished pharmaceutical products.
- Operate and maintain laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
- Execute analytical methods according to established Standard Operating Procedures (SOPs).
- Document all experimental procedures, observations, and results accurately and thoroughly in laboratory notebooks and electronic systems.
- Calibrate and qualify laboratory instruments as per schedule and specifications.
- Troubleshoot analytical methods and equipment failures, providing solutions to ensure uninterrupted testing.
- Analyze data, interpret results, and prepare Certificates of Analysis (CoA).
- Ensure compliance with cGMP, GLP, and relevant regulatory guidelines (e.g., FDA, EMA).
- Participate in internal and external audits related to quality control.
- Collaborate with R&D and production teams to address product quality issues and implement corrective actions.
- Contribute to method validation and verification activities.
- Maintain a clean, organized, and safe laboratory environment.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related scientific discipline.
- Minimum of 2-3 years of experience in a pharmaceutical quality control laboratory.
- Hands-on experience with analytical techniques such as HPLC, GC, spectroscopy, and titrimetry.
- Proficiency in GMP and GLP principles.
- Excellent understanding of pharmaceutical regulations.
- Strong data analysis and interpretation skills.
- Proficiency in laboratory information management systems (LIMS).
- Detail-oriented with excellent organizational and documentation skills.
- Good written and verbal communication skills.
- Ability to work effectively in a team environment and independently.
- Proficiency in Microsoft Office Suite.
This is an outstanding opportunity to join a forward-thinking pharmaceutical company in **Hamad Town, Northern, BH** and contribute to the development and manufacturing of high-quality medicines.
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7
Pharmaceutical Quality Control Analyst
450, 451 Seef, Capital
BHD65000 Annually
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Our esteemed client, a leading pharmaceutical company, is actively seeking a meticulous and driven Pharmaceutical Quality Control Analyst to join their team at their facility in Seef, Capital, BH . This critical role ensures that all pharmaceutical products meet stringent quality standards and regulatory requirements before they reach consumers. You will be involved in a wide range of analytical testing, laboratory procedures, and documentation processes, contributing directly to the safety and efficacy of our medications.
Your primary responsibilities will include performing in-process and finished product testing using various analytical techniques such as HPLC, GC, UV-Vis spectrophotometry, and titrations. You will be responsible for preparing reagents, maintaining laboratory equipment, and accurately documenting all test results in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). A keen eye for detail and a commitment to accuracy are paramount in this position.
The successful candidate will also play a role in method validation, stability studies, and troubleshooting analytical issues. You will work collaboratively with the research and development, manufacturing, and regulatory affairs departments to ensure seamless product development and lifecycle management. This is an excellent opportunity for a science-oriented individual looking to build a career in the vital pharmaceutical industry.
Key Responsibilities:
Your primary responsibilities will include performing in-process and finished product testing using various analytical techniques such as HPLC, GC, UV-Vis spectrophotometry, and titrations. You will be responsible for preparing reagents, maintaining laboratory equipment, and accurately documenting all test results in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). A keen eye for detail and a commitment to accuracy are paramount in this position.
The successful candidate will also play a role in method validation, stability studies, and troubleshooting analytical issues. You will work collaboratively with the research and development, manufacturing, and regulatory affairs departments to ensure seamless product development and lifecycle management. This is an excellent opportunity for a science-oriented individual looking to build a career in the vital pharmaceutical industry.
Key Responsibilities:
- Conducting analytical tests on raw materials, in-process samples, and finished pharmaceutical products.
- Operating and maintaining laboratory instruments (e.g., HPLC, GC, FTIR, UV-Vis).
- Documenting all experimental procedures and results accurately according to GMP/GLP.
- Preparing and standardizing chemical reagents and solutions.
- Participating in method validation and stability testing programs.
- Investigating out-of-specification (OOS) results and implementing corrective actions.
- Ensuring laboratory compliance with safety and regulatory guidelines.
- Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related scientific discipline.
- Previous experience in a pharmaceutical quality control or analytical laboratory setting is highly preferred.
- Hands-on experience with analytical instrumentation and techniques.
- Solid understanding of GMP, GLP, and regulatory requirements in the pharmaceutical industry.
- Strong attention to detail, critical thinking, and problem-solving abilities.
- Excellent organizational and record-keeping skills.
- Ability to work effectively in a team environment.
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8
Pharmaceutical Quality Control Analyst
25201 Al Jasra
BHD60000 Annually
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Job Description
Our client, a prestigious pharmaceutical company at the forefront of drug discovery and manufacturing, is seeking a diligent and analytical Pharmaceutical Quality Control Analyst to join their dedicated team in Hidd . This hybrid role offers the flexibility of remote work for certain analytical tasks while requiring on-site presence for laboratory-based quality control procedures. You will play a critical role in ensuring the quality, safety, and efficacy of our pharmaceutical products through rigorous testing and compliance monitoring.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform a variety of chemical and physical tests on raw materials, in-process samples, and finished pharmaceutical products using advanced analytical techniques and instrumentation (e.g., HPLC, GC, UV-Vis, FT-IR).
- Analyze test results, interpret data, and prepare detailed reports, ensuring accuracy and compliance with established specifications and regulatory guidelines (e.g., GMP, FDA, EMA).
- Maintain and calibrate laboratory equipment, ensuring optimal performance and adherence to calibration schedules.
- Develop, validate, and transfer analytical methods according to pharmaceutical industry standards.
- Document all laboratory activities meticulously in accordance with Good Manufacturing Practices (GMP) and company Standard Operating Procedures (SOPs).
- Investigate and resolve out-of-specification (OOS) results, identifying root causes and implementing corrective and preventive actions (CAPAs).
- Participate in internal and external audits, providing necessary documentation and explanations related to quality control processes.
- Collaborate with R&D, manufacturing, and regulatory affairs departments to support product development and lifecycle management.
- Monitor industry trends and regulatory updates relevant to pharmaceutical quality control.
- Contribute to the continuous improvement of quality systems and laboratory operations.
- Perform stability studies and analyze the data to determine product shelf-life.
- Ensure a safe laboratory environment by adhering to all safety protocols and guidelines.
Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Biochemistry, or a related life science discipline.
- Proven experience (2-4 years) in a pharmaceutical quality control or analytical laboratory setting.
- Hands-on experience with analytical instruments such as HPLC, GC, dissolution testers, and spectroscopy.
- Strong knowledge of GMP, regulatory requirements, and pharmacopoeial standards (USP, EP).
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in data analysis and scientific report writing.
- Familiarity with LIMS (Laboratory Information Management System) is a plus.
- Ability to work effectively both independently and as part of a collaborative team.
- Strong organizational skills and attention to detail.
- Adaptability to a hybrid work model, balancing remote analysis with essential on-site laboratory work.
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