What Jobs are available for Quality Control Analyst in Bahrain?

Showing 352 Quality Control Analyst jobs in Bahrain

Pharmaceutical Quality Control Analyst

90123 Zallaq, Southern BHD75000 Annually WhatJobs Direct

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Job Description

full-time
Our client, a reputable pharmaceutical company, is seeking a diligent and detail-oriented Pharmaceutical Quality Control Analyst to join their team in Zallaq, Southern, BH . This role offers a hybrid work model, involving laboratory work and data analysis.

You will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet strict quality standards and regulatory requirements. Your meticulous work will contribute directly to the safety and efficacy of the medicines we produce.

Key responsibilities:
  • Conduct analytical testing using various laboratory techniques, including HPLC, GC, UV-Vis, IR spectroscopy, and wet chemistry methods.
  • Prepare reagents, solutions, and standards required for testing.
  • Document all testing procedures and results accurately in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
  • Calibrate and maintain laboratory equipment, ensuring it is in optimal working condition.
  • Investigate out-of-specification (OOS) results and deviations, and participate in root cause analysis.
  • Analyze and interpret test data, preparing comprehensive reports.
  • Ensure compliance with all relevant regulatory guidelines (e.g., FDA, EMA).
  • Participate in method validation and transfer activities.
  • Contribute to the continuous improvement of quality control processes and laboratory operations.

Qualifications:
  • Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field.
  • Minimum of 3 years of experience in a pharmaceutical Quality Control laboratory environment.
  • Proficiency in analytical instrumentation commonly used in pharmaceutical QC (HPLC, GC, etc.).
  • Solid understanding of GMP, GLP, and regulatory requirements.
  • Strong analytical and problem-solving skills.
  • Excellent attention to detail and accuracy.
  • Good documentation and reporting skills.
  • Ability to work independently and as part of a team.

This is a crucial role within our Quality Assurance department, ensuring the integrity and quality of our pharmaceutical products. If you are passionate about quality and possess the required analytical skills, we encourage you to apply.
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Pharmaceutical Quality Control Analyst

231 Shahrakan BHD3200 Monthly WhatJobs Direct

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Job Description

full-time
Our client, a prominent pharmaceutical company, is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their state-of-the-art laboratory. This role is critical in ensuring the highest standards of quality and safety for all manufactured pharmaceutical products. You will be responsible for conducting a wide range of analytical tests on raw materials, in-process samples, and finished products using sophisticated laboratory equipment. The ideal candidate will possess a strong understanding of pharmaceutical quality systems, regulatory guidelines (e.g., GMP), and analytical chemistry principles. Key responsibilities include performing qualitative and quantitative analyses, validating test methods, maintaining accurate laboratory records, and troubleshooting analytical issues. You will also be involved in preparing technical reports and collaborating with production, R&D, and regulatory affairs teams to address any quality deviations or improvements. This position requires a Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related scientific discipline, coupled with practical experience in a pharmaceutical QC laboratory. Working in Budaiya, Northern, BH , you will operate within a highly regulated environment where precision and adherence to protocols are paramount. Experience with HPLC, GC, UV-Vis spectroscopy, and other relevant analytical techniques is essential. The ability to work efficiently under pressure, maintain strict confidentiality, and contribute to continuous quality improvement initiatives will be highly valued. This is an excellent opportunity for a detail-oriented scientist to contribute to the development and delivery of safe and effective medicines.

Responsibilities:
  • Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products.
  • Utilize various laboratory instruments such as HPLC, GC, UV-Vis, FTIR, and dissolution testers.
  • Ensure all testing is conducted according to established Standard Operating Procedures (SOPs) and regulatory guidelines (GMP).
  • Validate analytical methods and document results accurately and thoroughly.
  • Prepare and review certificates of analysis (CoAs) and analytical reports.
  • Maintain laboratory equipment, including calibration and performance verification.
  • Identify, investigate, and document out-of-specification (OOS) results and deviations.
  • Collaborate with production and R&D departments to resolve quality issues.
  • Contribute to the continuous improvement of quality control processes and systems.
  • Maintain a safe working environment and adhere to all safety protocols.
  • Assist in internal and external audits related to quality control.
  • Stay updated with relevant pharmaceutical regulations and industry best practices.
Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related science.
  • Proven experience as a Quality Control Analyst in the pharmaceutical industry.
  • In-depth knowledge of analytical techniques and instrumentation (HPLC, GC, etc.).
  • Familiarity with Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
  • Strong understanding of pharmaceutical product development and manufacturing processes.
  • Excellent attention to detail and accuracy in data recording and reporting.
  • Proficiency in using laboratory information management systems (LIMS).
  • Strong problem-solving and troubleshooting skills.
  • Effective written and verbal communication skills.
  • Ability to work independently and as part of a team in a fast-paced environment.
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Senior Quality Control Analyst

1002 Tubli BHD70000 Annually WhatJobs Direct

Posted 2 days ago

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Job Description

full-time
Our client is looking for a meticulous and experienced Senior Quality Control Analyst to ensure the highest standards of product quality. This hybrid role offers a blend of remote flexibility and in-person collaboration, providing a dynamic work environment. You will be responsible for developing, implementing, and overseeing quality control procedures and protocols throughout the production process. This includes performing rigorous testing, analyzing results, and identifying areas for improvement to maintain product integrity and compliance with industry regulations. A strong background in quality assurance methodologies and attention to detail are critical.

Key responsibilities:
  • Developing, implementing, and maintaining comprehensive quality control plans and SOPs.
  • Performing routine and non-routine testing of raw materials, in-process samples, and finished products.
  • Analyzing test results, identifying deviations, and investigating root causes of quality issues.
  • Documenting all quality control activities and maintaining accurate records.
  • Collaborating with production and R&D teams to address quality concerns and implement corrective actions.
  • Ensuring compliance with relevant regulatory standards and industry best practices.
  • Calibrating and maintaining laboratory equipment.
  • Preparing quality reports and presenting findings to management.
  • Contributing to continuous improvement initiatives to enhance product quality and process efficiency.
  • Training and mentoring junior quality control staff.

The ideal candidate will possess a Bachelor's degree in Chemistry, Biology, Pharmacy, or a related scientific field. A minimum of 5 years of experience in pharmaceutical quality control or assurance is required. Strong knowledge of analytical techniques (e.g., HPLC, GC, spectroscopy) and quality management systems (e.g., GMP, ISO) is essential. Excellent analytical, problem-solving, and documentation skills are necessary. Proficiency in data analysis and reporting is required. The ability to work effectively both independently and as part of a team in a hybrid setting is crucial for success in this role. This position, located in the vicinity of A'ali, Northern, BH , offers a significant opportunity to contribute to product excellence.
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Pharmaceutical Quality Control Analyst

222 Al Muharraq, Muharraq BHD50000 Annually WhatJobs

Posted 3 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a meticulous and dedicated Pharmaceutical Quality Control Analyst to join their team in Jidhafs, Capital, BH . This role is essential for ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You will perform a variety of laboratory tests on raw materials, in-process samples, and finished products, adhering strictly to Good Manufacturing Practices (GMP) and regulatory guidelines. The ideal candidate will possess a strong scientific background, exceptional attention to detail, and experience with analytical instrumentation.

Key Responsibilities:
  • Perform analytical testing on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis Spectroscopy, Karl Fischer titration).
  • Document all testing procedures and results accurately in compliance with GMP and regulatory standards.
  • Prepare reagents, standards, and samples for analysis.
  • Calibrate and maintain laboratory equipment to ensure accurate and reliable results.
  • Review and interpret test data, identifying any deviations or out-of-specification (OOS) results.
  • Investigate OOS results and deviations, and participate in root cause analysis.
  • Assist in the validation of analytical methods and equipment.
  • Ensure compliance with all safety procedures and maintain a clean and organized laboratory environment.
  • Collaborate with production, R&D, and regulatory affairs teams.
  • Contribute to continuous improvement initiatives within the Quality Control department.
  • Stay updated on relevant pharmacopoeias (e.g., USP, EP) and regulatory guidelines.
Qualifications:
  • Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
  • Minimum of 2-4 years of experience in pharmaceutical quality control or a related laboratory setting.
  • Hands-on experience with analytical techniques such as HPLC, GC, and spectrophotometry.
  • Familiarity with GMP, FDA, and other relevant regulatory requirements.
  • Strong understanding of pharmaceutical testing methodologies.
  • Excellent analytical, problem-solving, and documentation skills.
  • High level of accuracy and attention to detail.
  • Proficiency in Microsoft Office Suite.
  • Ability to work effectively in a team-oriented environment.
This is a crucial role for ensuring product integrity and patient safety.
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Pharmaceutical Quality Control Analyst

22222 Northern, Northern BHD55000 Annually WhatJobs

Posted 4 days ago

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Job Description

full-time
Our client, a reputable pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team in Shakhura, Northern, BH . This critical role involves performing a variety of laboratory tests and analyses to ensure the quality, safety, and efficacy of pharmaceutical products. You will be responsible for executing analytical procedures, maintaining laboratory equipment, documenting results accurately, and ensuring compliance with Good Manufacturing Practices (GMP) and other regulatory standards.

Key Responsibilities:
  • Conduct comprehensive analytical testing of raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, titration).
  • Prepare samples and reagents for testing.
  • Operate, calibrate, and maintain laboratory equipment to ensure accuracy and reliability of results.
  • Accurately record and document all test results, observations, and deviations in accordance with GMP guidelines and company SOPs.
  • Analyze test data, interpret results, and identify any out-of-specification (OOS) results.
  • Investigate OOS results and participate in the root cause analysis and corrective/preventive action (CAPA) process.
  • Perform stability studies and environmental monitoring as required.
  • Assist in the validation of analytical methods and laboratory equipment.
  • Ensure compliance with all safety regulations and maintain a clean and organized laboratory environment.
  • Participate in internal and external audits as required.
  • Review and update Standard Operating Procedures (SOPs) as necessary.
  • Maintain proficiency in analytical techniques and stay updated on industry advancements.
  • Collaborate effectively with other departments, including R&D, production, and regulatory affairs.
  • Prepare Certificates of Analysis (CoAs) for approved batches.
  • Contribute to a culture of quality and continuous improvement within the QC department.

The ideal candidate will possess a Bachelor's degree in Chemistry, Pharmacy, or a related life science field, coupled with proven experience in pharmaceutical quality control laboratory operations. Strong knowledge of GMP, analytical instrumentation, and regulatory requirements is essential. Excellent organizational skills, a meticulous approach to work, and the ability to manage multiple tasks efficiently are required. If you are dedicated to ensuring product quality and safety within the pharmaceutical industry, this is an excellent opportunity to grow your career.
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Pharmaceutical Quality Control Analyst

721 Al Malikiyah, Northern BHD70000 Annually WhatJobs

Posted 4 days ago

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Job Description

full-time
Our client is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst to join their dynamic team in Hamad Town, Northern, BH . This crucial role involves performing a wide range of analytical tests to ensure the quality, safety, and efficacy of pharmaceutical products. The ideal candidate will have a strong background in analytical chemistry, a keen eye for detail, and a commitment to upholding the highest quality standards within the pharmaceutical manufacturing process. This position requires hands-on laboratory work and adherence to strict regulatory guidelines.

Key Responsibilities:
  • Conduct routine and non-routine analytical testing of raw materials, in-process samples, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis spectroscopy, titrations).
  • Prepare reagents, standard solutions, and samples for analysis.
  • Calibrate and maintain laboratory equipment to ensure accurate and reliable results.
  • Document all testing procedures and results in accordance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) guidelines.
  • Investigate out-of-specification (OOS) results and deviations, identifying root causes and recommending corrective and preventive actions (CAPAs).
  • Participate in method validation and transfer activities.
  • Review and approve analytical test data and reports.
  • Assist in the development and optimization of analytical methods.
  • Maintain a clean and organized laboratory environment.
  • Contribute to internal and external audits by providing accurate documentation and demonstrating compliance.

Qualifications:
  • Bachelor's degree in Chemistry, Pharmacy, Biochemistry, or a related scientific field.
  • Minimum of 3 years of experience in a pharmaceutical quality control or analytical laboratory setting.
  • Proficiency in operating and maintaining analytical instruments such as HPLC, GC, and spectrophotometers.
  • Strong understanding of cGMP, GLP, and relevant regulatory requirements.
  • Excellent analytical, problem-solving, and critical thinking skills.
  • Meticulous attention to detail and accuracy in data recording and reporting.
  • Good written and verbal communication skills.
  • Ability to work independently and as part of a team.
  • Familiarity with laboratory information management systems (LIMS) is a plus.
  • Knowledge of pharmacopoeial methods (USP, BP, EP) is desirable.

This is an excellent opportunity for a dedicated analytical scientist to contribute to the quality assurance of essential pharmaceutical products in a stable and growing industry. Our client values precision, integrity, and continuous improvement.
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Pharmaceutical Quality Control Analyst

912 Jbeil BHD60000 Annually WhatJobs

Posted 4 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a meticulous and analytical Pharmaceutical Quality Control Analyst to join their esteemed team. This role is crucial in ensuring the quality and safety of our pharmaceutical products through rigorous testing and analysis. The position is based in **Sanad, Capital, BH**, with a hybrid work arrangement allowing for a balance between in-office and remote work. You will be responsible for performing a variety of analytical tests on raw materials, in-process samples, and finished products using advanced laboratory techniques and instrumentation, such as HPLC, GC, and spectrophotometry. This includes method development, validation, and routine testing in compliance with Good Manufacturing Practices (GMP) and regulatory guidelines. You will meticulously document all testing procedures and results, prepare analytical reports, and investigate any out-of-specification (OOS) results. Collaboration with the R&D, Manufacturing, and Regulatory Affairs departments will be a key aspect of this role, ensuring that all quality standards are met throughout the product lifecycle. The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related life science field, coupled with practical experience in a pharmaceutical QC laboratory setting. Strong understanding of analytical chemistry principles, regulatory requirements (e.g., FDA, EMA), and GMP is essential. Excellent data analysis, critical thinking, and problem-solving skills are required, along with exceptional attention to detail and strong written and verbal communication abilities. This is an excellent opportunity to contribute to the development and production of life-saving medications within a supportive and growth-oriented environment.
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Pharmaceutical Quality Control Analyst

2013 Al Burhama BHD65000 Annually WhatJobs

Posted 5 days ago

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Job Description

full-time
Our client is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their team in Hidd, Muharraq, BH . This role is crucial in ensuring the quality, safety, and efficacy of pharmaceutical products manufactured by the company. The Analyst will be responsible for performing a wide range of laboratory tests on raw materials, in-process samples, and finished products according to established protocols and regulatory guidelines. This includes utilizing various analytical instruments such as HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.

Key duties involve preparing reagents, standardizing solutions, and accurately recording and analyzing test results. The successful candidate will also be involved in method validation, instrument calibration, and routine maintenance of laboratory equipment. A critical aspect of this role is adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), ensuring all activities are performed in compliance with regulatory requirements set forth by authorities like the FDA and EMA. The analyst will contribute to maintaining a robust quality management system, investigating out-of-specification (OOS) results, and participating in root cause analysis investigations.

Furthermore, the Pharmaceutical Quality Control Analyst will be expected to contribute to the continuous improvement of QC processes and procedures, assist in the preparation of quality reports, and support regulatory inspections and audits. Strong understanding of pharmaceutical chemistry, analytical techniques, and regulatory compliance is essential. Excellent laboratory technique, data integrity, and problem-solving skills are paramount for success in this position. This role offers a great opportunity to contribute to the development and production of life-saving medicines in Hidd, Muharraq, BH .

Responsibilities:
  • Perform quantitative and qualitative analyses on raw materials, intermediates, and finished pharmaceutical products.
  • Operate and maintain analytical instruments (e.g., HPLC, GC, UV-Vis, FTIR).
  • Prepare chemical reagents and solutions accurately.
  • Document all laboratory activities, test results, and deviations meticulously.
  • Ensure compliance with GLP, GMP, and other relevant regulatory standards.
  • Investigate Out-of-Specification (OOS) results and participate in CAPA activities.
  • Perform method validation and instrument qualification/calibration.
  • Contribute to the development and revision of QC procedures.
  • Prepare technical reports and summaries of analytical data.
  • Support internal and external audits and regulatory inspections.
Qualifications:
  • Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related life science field.
  • Proven experience in a pharmaceutical Quality Control laboratory setting.
  • Hands-on experience with common analytical techniques and instrumentation.
  • Knowledge of ICH guidelines, GMP, and regulatory requirements.
  • Strong analytical and problem-solving abilities.
  • Excellent attention to detail and data integrity.
  • Proficiency in laboratory documentation and report writing.
  • Ability to work effectively both independently and in a team environment.
Join our client's dedicated team and contribute to pharmaceutical excellence in Hidd, Muharraq, BH .
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Pharmaceutical Quality Control Analyst

701 Hamad Town, Northern BHD60000 Annually WhatJobs

Posted 6 days ago

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Job Description

full-time
Our client, a prominent pharmaceutical company located in Hamad Town, Northern, BH , is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst. This critical role ensures that all manufactured pharmaceutical products meet stringent quality and safety standards before they reach the market. You will be responsible for performing a wide range of laboratory tests on raw materials, in-process samples, and finished products using various analytical techniques and instruments, such as HPLC, GC, UV-Vis spectrophotometry, and titration. Accurate documentation of all test results, adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), and participation in method validation studies are core responsibilities. You will also be involved in investigating out-of-specification (OOS) results, identifying root causes, and implementing corrective and preventive actions (CAPA). Maintaining laboratory equipment, ensuring it is calibrated and properly functioning, and managing laboratory supplies are also essential duties. The analyst will contribute to the continuous improvement of quality control processes and systems. Collaboration with R&D, Production, and Regulatory Affairs departments to resolve quality issues and ensure product compliance will be a regular part of the job. The ideal candidate will possess a Bachelor's or Master's degree in Pharmacy, Chemistry, or a related science field, along with hands-on experience in pharmaceutical quality control. Strong analytical skills, a thorough understanding of pharmaceutical quality systems, and excellent record-keeping abilities are paramount. Knowledge of relevant regulatory guidelines (e.g., FDA, EMA) is highly desirable. This position offers a challenging and rewarding career in a vital industry.
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Pharmaceutical Quality Control Analyst

00973 Busaiteen, Muharraq BHD65000 Annually WhatJobs

Posted 7 days ago

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Job Description

full-time
Our client, a leading pharmaceutical company, is seeking a diligent and experienced Pharmaceutical Quality Control Analyst for a fully remote position. This is a crucial role in ensuring the safety, efficacy, and quality of pharmaceutical products through rigorous testing and analysis. You will be responsible for performing a variety of laboratory tests on raw materials, in-process samples, and finished products to ensure they meet established specifications and regulatory standards. Your duties will include operating and maintaining laboratory equipment, developing and validating analytical methods, and documenting all testing procedures and results accurately. Strong knowledge of analytical chemistry techniques (e.g., HPLC, GC, spectroscopy) and pharmacopeial methods is essential. You will play a key role in identifying deviations, investigating out-of-specification (OOS) results, and contributing to the implementation of corrective and preventive actions (CAPA). The ideal candidate will possess excellent scientific understanding, meticulous attention to detail, and a commitment to upholding the highest quality standards. This remote role requires strong organizational skills, the ability to work independently, and effective communication with R&D, manufacturing, and regulatory affairs teams. Our client values individuals who are proactive, analytical, and dedicated to continuous improvement in quality systems. If you are a qualified analyst passionate about contributing to pharmaceutical quality assurance in a remote capacity, we encourage you to apply. Your expertise will directly contribute to the delivery of safe and effective medicines to patients worldwide.

Key Responsibilities:
  • Perform analytical testing on raw materials, in-process samples, and finished products.
  • Operate, calibrate, and maintain laboratory equipment (e.g., HPLC, GC, UV-Vis spectrophotometer).
  • Develop, validate, and transfer analytical methods.
  • Document all laboratory procedures, results, and deviations according to SOPs and GMP guidelines.
  • Investigate out-of-specification (OOS) results and out-of-trend (OOT) data.
  • Contribute to the implementation of corrective and preventive actions (CAPA).
  • Ensure compliance with Good Manufacturing Practices (GMP) and relevant regulatory requirements.
  • Prepare and review quality control reports and certificates of analysis.
  • Collaborate with cross-functional teams to resolve quality-related issues.
Qualifications:
  • Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
  • Proven experience as a Quality Control Analyst in the pharmaceutical industry.
  • Strong knowledge of analytical chemistry techniques and instrumentation.
  • Familiarity with pharmacopeial methods (e.g., USP, EP).
  • Understanding of GMP, ICH guidelines, and regulatory requirements.
  • Excellent analytical, problem-solving, and documentation skills.
  • Ability to work independently and manage time effectively in a remote setting.
  • Strong written and verbal communication skills.
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