What Jobs are available for Quality Control Analysts in Bahrain?
Showing 368 Quality Control Analysts jobs in Bahrain
Pharmaceutical Quality Control Analyst
Posted today
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Job Description
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
Posted today
Job Viewed
Job Description
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.
- 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
Posted 2 days ago
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Job Description
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
Posted 3 days ago
Job Viewed
Job Description
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.
- 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.
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            Pharmaceutical Quality Control Analyst
Posted 4 days ago
Job Viewed
Job Description
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
Posted 4 days ago
Job Viewed
Job Description
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
Posted 4 days ago
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Job Description
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Pharmaceutical Quality Control Analyst
Posted 5 days ago
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Job Description
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.
- 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.
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            Pharmaceutical Quality Control Analyst
Posted 6 days ago
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Job Description
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            Pharmaceutical Quality Control Analyst
Posted 7 days ago
Job Viewed
Job Description
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.
- 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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