270 Quality Control Analyst jobs in Bahrain
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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0
Pharmaceutical Quality Control Analyst
25201 Al Jasra
BHD60000 Annually
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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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1
Pharmaceutical Quality Control Analyst
400 Diplomatic Area
BHD70000 Annually
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Our client, a growing pharmaceutical company, is seeking a meticulous and analytical Pharmaceutical Quality Control Analyst to join their team in **Isa Town, Southern, BH**. This role is crucial in ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. You will be responsible for conducting a variety of laboratory tests on raw materials, in-process samples, and finished products using advanced analytical techniques and instrumentation. Key responsibilities include performing assays, identifying impurities, and verifying product specifications through methods such as HPLC, GC, UV-Vis spectroscopy, and titration. You will meticulously document all test results, maintain laboratory equipment, and ensure compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). A significant part of this role involves reviewing batch records, investigating deviations and out-of-specification (OOS) results, and participating in the development and validation of new analytical methods. You will collaborate with R&D, production, and regulatory affairs departments to resolve quality issues and ensure product integrity. The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, or a related life science field, with at least 3 years of experience in pharmaceutical quality control or quality assurance. Hands-on experience with analytical instrumentation common in the pharmaceutical industry is mandatory. A thorough understanding of pharmaceutical regulations (e.g., FDA, EMA) and quality systems is essential. Excellent attention to detail, strong analytical and problem-solving skills, and proficient documentation abilities are required. This is an exciting opportunity to contribute to the development and production of life-saving medicines and advance your career in pharmaceutical quality assurance.
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2
Pharmaceutical Quality Control Analyst
1080 Zallaq, Southern
BHD22000 Annually
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Our client, a leading pharmaceutical company, is seeking a meticulous and skilled Pharmaceutical Quality Control Analyst to join their team in **Zallaq, Southern, BH**. This critical role ensures that our pharmaceutical products meet the highest standards of quality, safety, and efficacy. The analyst will be responsible for performing a variety of laboratory tests, analyzing results, and documenting findings in compliance with regulatory guidelines. This is an excellent opportunity for a scientifically inclined individual to contribute to the development and production of life-saving medications.
Key Responsibilities:
Key Responsibilities:
- Perform in-process and finished product testing using various analytical techniques (e.g., HPLC, GC, UV-Vis spectroscopy).
- Analyze and interpret test data to determine product compliance with specifications.
- Prepare reagents, solutions, and standard operating procedures (SOPs) for laboratory testing.
- Maintain accurate and detailed laboratory records, including batch records and analytical reports.
- Calibrate and maintain laboratory equipment to ensure accuracy and reliability.
- Participate in method validation and transfer activities.
- Investigate out-of-specification (OOS) results and deviations, and assist in root cause analysis.
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements.
- Collaborate with production, R&D, and regulatory affairs departments.
- Contribute to the continuous improvement of quality control processes and laboratory operations.
- Handle and dispose of chemical waste according to safety protocols.
- Train junior analysts on laboratory procedures and techniques.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
- Proven experience in pharmaceutical quality control or a related laboratory setting.
- Hands-on experience with common analytical instruments (HPLC, GC, spectroscopy).
- Strong understanding of GMP, FDA regulations, and quality assurance principles.
- Excellent analytical, problem-solving, and critical thinking skills.
- Proficiency in laboratory data management and reporting.
- Detail-oriented with a strong commitment to accuracy.
- Good communication and teamwork abilities.
- Ability to work independently and manage multiple tasks effectively.
- Familiarity with relevant software for data analysis and record-keeping.
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3
Pharmaceutical Quality Control Analyst
101 Bilad Al Qadeem, Capital
BHD60000 Annually
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Our client, a leading pharmaceutical company, is seeking a meticulous and skilled Pharmaceutical Quality Control Analyst to join their esteemed team in **Sitra, Capital, BH**. This role is integral to ensuring the consistent quality, safety, and efficacy of our pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a strong foundation in analytical chemistry, laboratory techniques, and quality assurance principles within the pharmaceutical industry. You will be responsible for performing a wide range of tests on raw materials, in-process samples, and finished products, ensuring compliance with regulatory standards and internal specifications.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform a variety of analytical tests on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis, FTIR, and dissolution testing.
- Prepare reagents, solutions, and standards required for testing.
- Calibrate and maintain laboratory equipment to ensure accurate and reliable results.
- Document all testing procedures, results, and observations meticulously in accordance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Analyze test data, interpret results, and prepare comprehensive analytical reports.
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and recommending corrective actions.
- Participate in method validation and transfer activities.
- Maintain laboratory inventory and ensure the proper storage and handling of chemicals and samples.
- Adhere strictly to all safety protocols and environmental regulations within the laboratory.
- Collaborate with R&D, Production, and Quality Assurance departments to address product quality issues.
- Assist in the training of junior laboratory personnel.
- Stay current with pharmacopeial requirements (e.g., USP, EP) and regulatory guidelines.
- Ensure compliance with all cGMP requirements.
Qualifications:
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 3 years of hands-on experience in a pharmaceutical quality control laboratory setting.
- Proficiency in operating and maintaining analytical instrumentation common in pharmaceutical QC labs (HPLC, GC, UV-Vis, etc.).
- Strong understanding of GMP, GLP, and regulatory requirements for the pharmaceutical industry.
- Excellent data analysis, documentation, and report-writing skills.
- Detail-oriented with a strong commitment to accuracy and quality.
- Ability to work independently and as part of a team.
- Good problem-solving skills and the ability to troubleshoot analytical issues.
- Proficiency in Microsoft Office Suite and laboratory information management systems (LIMS) is a plus.
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4
Pharmaceutical Quality Control Analyst
21102 Hamad Town, Northern
BHD60000 Annually
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Our client, a leading biopharmaceutical company renowned for its cutting-edge research and development, is seeking a diligent and detail-oriented Pharmaceutical Quality Control Analyst to join their esteemed laboratory team in **Hamad Town, Northern, BH**. This vital role is responsible for ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. The ideal candidate will possess a strong background in analytical chemistry, a thorough understanding of pharmaceutical quality standards, and a commitment to maintaining the highest levels of regulatory compliance. You will be a key contributor to our mission of delivering high-quality medicines to patients worldwide.
Key Responsibilities:
Key Responsibilities:
- Perform a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various laboratory instruments and techniques (e.g., HPLC, GC, UV-Vis, FTIR).
- Ensure all testing is conducted in accordance with approved Standard Operating Procedures (SOPs), pharmacopoeial standards (USP, EP), and regulatory guidelines (e.g., GMP, ICH).
- Accurately document all experimental procedures, results, and observations in laboratory notebooks and electronic systems.
- Calibrate, maintain, and troubleshoot laboratory equipment to ensure optimal performance and accuracy.
- Analyze test data, interpret results, and prepare Certificates of Analysis (CoA) and detailed analytical reports.
- Identify and report any deviations from established procedures or out-of-specification (OOS) results, and participate in investigations.
- Maintain a clean, organized, and safe laboratory environment, adhering to all safety protocols.
- Participate in method validation and transfer activities as required.
- Collaborate with R&D, production, and regulatory affairs teams to resolve quality-related issues.
- Review and update laboratory SOPs and test methods as necessary.
- Ensure compliance with all Good Manufacturing Practices (GMP) and relevant quality systems.
- Contribute to the continuous improvement of laboratory processes and analytical methods.
- Manage laboratory inventory and order necessary reagents and supplies.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biochemistry, or a related scientific discipline.
- Minimum of 3-5 years of experience in pharmaceutical quality control or a related analytical laboratory setting.
- Hands-on experience with common pharmaceutical analytical techniques and instrumentation (HPLC, GC, dissolution testing, spectroscopy).
- Strong understanding of pharmaceutical manufacturing processes and quality systems (GMP).
- Proficiency in pharmacopoeial standards (USP, EP, BP) and ICH guidelines.
- Excellent analytical, problem-solving, and critical thinking skills.
- Meticulous attention to detail and accuracy in data recording and reporting.
- Good organizational and time management skills.
- Ability to work independently and collaboratively in a team environment.
- Proficiency in Microsoft Office Suite and laboratory information management systems (LIMS) is a plus.
- Strong written and verbal communication skills.
- Commitment to upholding quality standards and ensuring product integrity.
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5
Pharmaceutical Quality Control Analyst
54321 Riffa, Southern
BHD60000 Annually
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Our client is seeking a detail-oriented and diligent Pharmaceutical Quality Control Analyst to join their QC laboratory in Riffa, Southern, BH . This role is essential for ensuring the quality and compliance of pharmaceutical products by performing rigorous testing and analysis. The successful candidate will be responsible for executing various analytical methods and contributing to the overall quality assurance of manufactured drugs.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform in-process and finished product testing using a variety of analytical techniques, including HPLC, GC, UV-Vis, and wet chemistry.
- Prepare samples for analysis and ensure proper handling and storage of laboratory materials.
- Document all testing procedures and results accurately and in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
- Calibrate and maintain laboratory equipment, ensuring proper functioning and accuracy.
- Troubleshoot analytical methods and equipment malfunctions.
- Interpret test results and compare them against established specifications.
- Investigate out-of-specification (OOS) results and deviations, participating in root cause analysis.
- Prepare Certificates of Analysis (CoA) for raw materials, intermediates, and finished products.
- Contribute to the validation of new analytical methods and the transfer of methods from R&D.
- Maintain a clean and organized laboratory workspace.
Qualifications:
- Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- Minimum of 3 years of experience working in a pharmaceutical Quality Control laboratory.
- Hands-on experience with analytical instrumentation such as HPLC, GC, FTIR, and dissolution testers.
- Thorough understanding of GMP, GLP, and pharmacopeial standards (e.g., USP, EP).
- Proficiency in data recording, laboratory notebook maintenance, and report writing.
- Strong attention to detail and accuracy in all tasks.
- Ability to work independently and as part of a team in a fast-paced environment.
- Excellent problem-solving and critical thinking skills.
- Familiarity with stability testing protocols.
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6
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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7
Pharmaceutical Quality Control Analyst
13456 Bilad Al Qadeem, Capital
BHD60000 Annually
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Our client, a leading pharmaceutical company, is seeking a diligent and detail-oriented Pharmaceutical Quality Control Analyst to join their team in **Sitra, Capital, BH**. This role offers a hybrid work arrangement, blending on-site laboratory work with some remote analysis and reporting. You will be instrumental in ensuring the quality and safety of our pharmaceutical products by performing rigorous testing and analysis throughout the manufacturing process. This position requires a strong scientific background and a meticulous approach to quality assurance.
Your responsibilities will encompass:
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science discipline. Previous experience in a pharmaceutical quality control laboratory setting is highly desirable. Proficiency with analytical instrumentation and strong understanding of analytical methodologies are essential. Knowledge of GMP, GLP, and regulatory requirements within the pharmaceutical industry is crucial. Excellent analytical and problem-solving skills, attention to detail, and the ability to work effectively in a team environment are required. Strong written and verbal communication skills are necessary for report writing and cross-functional collaboration. This role demands a commitment to scientific integrity and product quality.
Your responsibilities will encompass:
- Conducting chemical and physical analyses of raw materials, in-process samples, and finished pharmaceutical products using various laboratory techniques.
- Performing tests according to established Standard Operating Procedures (SOPs) and pharmacopoeial standards.
- Operating and maintaining laboratory equipment, including HPLC, GC, UV-Vis spectrophotometers, and dissolution testers.
- Documenting all experimental procedures, results, and observations accurately and comprehensively in laboratory notebooks and electronic systems.
- Evaluating test results, identifying any deviations from specifications, and investigating out-of-specification (OOS) results.
- Preparing and reviewing analytical reports and quality control documentation.
- Ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and relevant regulatory guidelines.
- Participating in method validation and verification activities.
- Collaborating with research and development, production, and regulatory affairs teams.
- Maintaining a clean, organized, and safe laboratory environment.
The ideal candidate will hold a Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science discipline. Previous experience in a pharmaceutical quality control laboratory setting is highly desirable. Proficiency with analytical instrumentation and strong understanding of analytical methodologies are essential. Knowledge of GMP, GLP, and regulatory requirements within the pharmaceutical industry is crucial. Excellent analytical and problem-solving skills, attention to detail, and the ability to work effectively in a team environment are required. Strong written and verbal communication skills are necessary for report writing and cross-functional collaboration. This role demands a commitment to scientific integrity and product quality.
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8
Pharmaceutical Quality Control Analyst
1075 Tubli, Central
BHD60000 Annually
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Our client is looking for a meticulous and experienced Pharmaceutical Quality Control Analyst to ensure the quality and integrity of their pharmaceutical products. This role is vital for maintaining compliance with regulatory standards and ensuring the safety and efficacy of medicines. The Quality Control Analyst will be responsible for performing a variety of laboratory tests and analyses on raw materials, in-process samples, and finished products. You will maintain accurate records, calibrate laboratory equipment, and contribute to the development and validation of analytical methods. This hybrid role involves both laboratory-based work and administrative tasks such as data review and report generation. The ideal candidate possesses strong analytical skills, a deep understanding of pharmaceutical quality systems, and meticulous attention to detail. Responsibilities include: performing a wide range of analytical tests on pharmaceutical raw materials, intermediates, and finished products using various laboratory techniques (e.g., HPLC, GC, UV-Vis, Karl Fischer); preparing samples and reagents for testing; operating and maintaining laboratory equipment, including calibration and qualification; documenting all test results accurately and thoroughly in accordance with GMP guidelines; reviewing and analyzing data to ensure compliance with specifications; investigating out-of-specification (OOS) results and implementing corrective actions; participating in the validation of analytical methods and equipment; ensuring adherence to all company policies, SOPs, and regulatory requirements (e.g., FDA, EMA); maintaining a clean and organized laboratory environment; contributing to continuous improvement initiatives within the quality control department. Qualifications include a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field. A Master's degree is a plus. A minimum of 4 years of experience in pharmaceutical quality control or a related laboratory setting is required. Hands-on experience with analytical instrumentation commonly used in the pharmaceutical industry is essential. Strong knowledge of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) is mandatory. Excellent data interpretation, documentation, and problem-solving skills are crucial. Proficiency in laboratory information management systems (LIMS) is desirable. This position requires a commitment to maintaining high-quality standards in a regulated environment.
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