65 Quality Control Analyst jobs in Bahrain
Pharmaceutical Quality Control Analyst
2042 Zallaq, Southern
BHD60000 Annually
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Our client, a reputable pharmaceutical manufacturing company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Control Analyst to join their laboratory team in Zallaq, Southern, BH . This role is integral to ensuring the quality, safety, and efficacy of pharmaceutical products through rigorous testing and analysis. You 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. The successful candidate will contribute significantly to maintaining the highest standards of pharmaceutical quality. Key responsibilities include:
Requirements include a Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related life science discipline. A minimum of 3 years of hands-on experience in pharmaceutical quality control laboratory settings is essential. Proficiency in operating and maintaining common analytical instruments (HPLC, GC) and a strong understanding of pharmaceutical quality systems and regulatory requirements (GMP/GLP) are mandatory. Excellent analytical, problem-solving, and documentation skills are crucial. The ability to work accurately under pressure and as part of a team is also important.
- Performing analytical testing on raw materials, intermediates, and finished pharmaceutical products using various laboratory techniques such as HPLC, GC, UV-Vis spectroscopy, Karl Fischer titration, and dissolution testing.
- Documenting all testing procedures, results, and observations accurately and thoroughly in laboratory notebooks and electronic systems, ensuring compliance with Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP).
- Calibrating, maintaining, and troubleshooting laboratory equipment to ensure its optimal performance and accuracy.
- Preparing reagents, solutions, and standards required for analytical testing.
- Reviewing and interpreting analytical data, comparing results against predefined specifications and identifying any out-of-specification (OOS) results.
- Investigating OOS results, participating in root cause analysis, and implementing corrective and preventive actions (CAPAs).
- Participating in method validation and transfer activities for new analytical methods or instruments.
- Ensuring compliance with all company quality policies, standard operating procedures (SOPs), and relevant regulatory guidelines (e.g., FDA, EMA, local health authorities).
- Maintaining a safe and organized laboratory environment, adhering to all safety protocols and waste disposal procedures.
- Contributing to internal audits and regulatory inspections by providing necessary documentation and information.
- Collaborating effectively with other departments, including R&D, Production, and Quality Assurance, to resolve quality-related issues.
Requirements include a Bachelor's degree in Chemistry, Pharmaceutical Sciences, or a related life science discipline. A minimum of 3 years of hands-on experience in pharmaceutical quality control laboratory settings is essential. Proficiency in operating and maintaining common analytical instruments (HPLC, GC) and a strong understanding of pharmaceutical quality systems and regulatory requirements (GMP/GLP) are mandatory. Excellent analytical, problem-solving, and documentation skills are crucial. The ability to work accurately under pressure and as part of a team is also important.
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Pharmaceutical Quality Control Analyst
BH 44444 Al Seef
BHD75000 Annually
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Our client, a leading pharmaceutical company, is seeking a meticulous and experienced Pharmaceutical Quality Control Analyst for a fully remote position. This role is critical in ensuring the quality and compliance of pharmaceutical products. You will be responsible for conducting a wide range of laboratory tests and analyses on raw materials, in-process samples, and finished products to verify they meet established specifications and regulatory standards. Your duties will include performing chemical and physical analyses using various analytical techniques and instrumentation (e.g., HPLC, GC, spectroscopy), maintaining accurate and detailed laboratory records, preparing test results and reports for review, and ensuring adherence to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP).
The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related life science field, along with demonstrable experience in pharmaceutical quality control. A strong understanding of analytical chemistry principles and experience with laboratory equipment are essential. Familiarity with regulatory guidelines from agencies such as the FDA and EMA is required. Excellent organizational skills, meticulous attention to detail, and strong problem-solving abilities are crucial for this role. As this is a remote position, you must be a self-disciplined, proactive individual with exceptional written and verbal communication skills, capable of managing your workload effectively and collaborating with on-site teams. Experience with data analysis software and a commitment to maintaining high standards of quality and compliance are highly valued. This is a unique opportunity to contribute to the safety and efficacy of pharmaceutical products from the comfort of your home. Join our client's dedicated quality assurance team and play a vital role in upholding the highest standards in the pharmaceutical industry.
The ideal candidate will possess a Bachelor's or Master's degree in Chemistry, Pharmacy, Biology, or a related life science field, along with demonstrable experience in pharmaceutical quality control. A strong understanding of analytical chemistry principles and experience with laboratory equipment are essential. Familiarity with regulatory guidelines from agencies such as the FDA and EMA is required. Excellent organizational skills, meticulous attention to detail, and strong problem-solving abilities are crucial for this role. As this is a remote position, you must be a self-disciplined, proactive individual with exceptional written and verbal communication skills, capable of managing your workload effectively and collaborating with on-site teams. Experience with data analysis software and a commitment to maintaining high standards of quality and compliance are highly valued. This is a unique opportunity to contribute to the safety and efficacy of pharmaceutical products from the comfort of your home. Join our client's dedicated quality assurance team and play a vital role in upholding the highest standards in the pharmaceutical industry.
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1
Pharmaceutical Quality Control Analyst
30055 Muharraq, Muharraq
BHD65000 Annually
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Our client, a leading pharmaceutical company committed to developing life-saving medications, is looking for a meticulous and experienced Pharmaceutical Quality Control Analyst. This critical role ensures the highest standards of product quality and regulatory compliance throughout the manufacturing process. The Analyst will perform a variety of laboratory tests on raw materials, in-process samples, and finished products to verify their identity, purity, potency, and overall quality. Responsibilities include operating and maintaining analytical instrumentation, preparing test solutions, documenting test results accurately and thoroughly in compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), and participating in method validation studies. The ideal candidate will possess a strong background in analytical chemistry, with hands-on experience in techniques such as HPLC, GC, UV-Vis spectrophotometry, and titrations. A Bachelor's or Master's degree in Chemistry, Pharmacy, or a related scientific field is required. Excellent attention to detail, strong problem-solving skills, and the ability to work independently as well as part of a team are essential. Our client is dedicated to scientific rigor and patient safety, and this role plays a pivotal part in upholding these values. This is an excellent opportunity to contribute to the pharmaceutical industry and advance your career in a challenging and rewarding environment. Join a team of dedicated professionals committed to improving global health outcomes. This role is located in Muharraq, Muharraq, BH .
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Senior Pharmaceutical Quality Control Analyst
70202 Zallaq, Southern
BHD85000 Annually
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Our client, a leading pharmaceutical company operating in **Zallaq, Southern, BH **, is seeking a highly meticulous and experienced Senior Pharmaceutical Quality Control Analyst. This critical role ensures the quality, safety, and efficacy of our pharmaceutical products through rigorous testing and analysis. You will be responsible for executing a wide range of analytical methods, maintaining laboratory equipment, and contributing to the overall quality assurance framework.
Responsibilities:
Responsibilities:
- Perform analytical testing of raw materials, in-process samples, and finished products using various techniques (e.g., HPLC, GC, spectroscopy, titration).
- Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH, FDA, GMP).
- Interpret test results, document findings accurately, and prepare detailed analytical reports.
- Maintain and calibrate laboratory instrumentation, ensuring compliance with standard operating procedures (SOPs) and calibration schedules.
- Troubleshoot analytical equipment and methods, identifying and resolving issues promptly.
- Ensure all laboratory activities comply with Good Manufacturing Practices (GMP) and other relevant regulatory requirements.
- Participate in internal and external audits, providing necessary documentation and support.
- Contribute to quality risk assessments and continuous improvement initiatives within the QC department.
- Stay updated with the latest advancements in pharmaceutical analysis and quality control.
- Train and mentor junior QC analysts on analytical techniques and laboratory procedures.
- Bachelor's degree in Pharmacy, Chemistry, Pharmaceutical Sciences, or a related discipline. Master's degree preferred.
- Minimum of 7 years of experience in pharmaceutical quality control or analytical development.
- Strong hands-on experience with analytical instrumentation such as HPLC, GC, UV-Vis, FTIR, and dissolution testers.
- In-depth knowledge of pharmaceutical GMP, regulatory guidelines, and quality systems.
- Proven ability in method development, validation, and troubleshooting.
- Excellent analytical, problem-solving, and documentation skills.
- Strong attention to detail and ability to work independently and as part of a team.
- Familiarity with laboratory information management systems (LIMS) is a plus.
- Experience working within the **Zallaq, Southern, BH ** region is advantageous.
- Excellent communication and interpersonal skills.
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3
Senior Pharmaceutical Quality Control Analyst
1099 Riffa, Southern
BHD70000 Annually
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Our client is seeking a highly skilled and meticulous Senior Pharmaceutical Quality Control Analyst to join their expanding team. This is an on-site role where you will be instrumental in ensuring the quality and integrity of pharmaceutical products through rigorous testing and analysis. You will perform a variety of laboratory tests using sophisticated analytical instruments and techniques, interpret results, and document findings in accordance with strict regulatory guidelines. The ideal candidate will have a strong background in pharmaceutical quality control, a thorough understanding of GMP (Good Manufacturing Practices), and excellent analytical and problem-solving abilities.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Perform in-process and finished product testing using various analytical techniques (e.g., HPLC, GC, UV-Vis, FTIR).
- Develop, validate, and transfer analytical methods as per ICH guidelines.
- Analyze raw materials, intermediates, and finished pharmaceutical products for identity, purity, strength, and quality.
- Interpret analytical data, troubleshoot method deviations, and document all testing activities accurately and meticulously.
- Investigate Out-of-Specification (OOS) and Out-of-Trend (OOT) results, identifying root causes and implementing corrective actions.
- Prepare Certificates of Analysis (CoA) and other quality control documentation.
- Maintain laboratory equipment, ensuring proper calibration, qualification, and maintenance.
- Adhere to all Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and safety regulations.
- Participate in internal and external audits as a subject matter expert.
- Train and mentor junior QC analysts on testing procedures and analytical techniques.
- Contribute to the continuous improvement of QC processes and laboratory operations.
Qualifications:
- Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field. Master's degree preferred.
- Minimum of 5 years of hands-on experience in pharmaceutical quality control or analytical development.
- Extensive experience with analytical instrumentation such as HPLC, GC, dissolution testers, and spectrophotometers.
- Strong knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceutical manufacturing.
- Proficiency in data analysis and interpretation, with excellent attention to detail.
- Experience in method validation and troubleshooting is essential.
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team in a fast-paced laboratory environment.
- Proficiency in LIMS (Laboratory Information Management System) is a plus.
- Commitment to quality, safety, and regulatory compliance.
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Senior Pharmaceutical Quality Control Analyst
176 Busaiteen, Muharraq
BHD70000 Annually
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Posted 2 days ago
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Our client, a leader in the pharmaceutical industry, is seeking a meticulous and highly skilled Senior Pharmaceutical Quality Control Analyst for their facility in Busaiteen, Muharraq, BH . This critical role involves performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet stringent quality and regulatory standards. The ideal candidate will possess a strong foundation in analytical chemistry, extensive experience with laboratory equipment, and a thorough understanding of Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). You will be responsible for method validation, data interpretation, and troubleshooting analytical procedures.
Key Responsibilities:
Key Responsibilities:
- Conducting analytical testing on pharmaceutical raw materials, intermediates, and finished products using various instrumental and wet chemistry techniques (e.g., HPLC, GC, UV-Vis, FTIR, Karl Fischer titration).
- Developing, validating, and transferring analytical methods according to regulatory guidelines.
- Interpreting test results, generating reports, and documenting all laboratory activities accurately.
- Ensuring compliance with GMP, GLP, and other relevant regulatory requirements.
- Troubleshooting analytical instrumentation and resolving method-related issues.
- Calibrating and maintaining laboratory equipment to ensure optimal performance.
- Participating in internal and external audits.
- Collaborating with R&D, production, and regulatory affairs departments to address quality-related issues.
- Reviewing and approving analytical data and documentation.
- Staying current with pharmacopeial methods and regulatory updates.
- Mentoring junior analysts and providing technical training.
- Contributing to continuous improvement initiatives within the QC department.
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5
Senior Pharmaceutical Quality Control Analyst
21205 Jbeil
BHD70000 Annually
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Our client, a rapidly expanding pharmaceutical company committed to producing high-quality medications, is actively seeking a Senior Pharmaceutical Quality Control Analyst for their state-of-the-art facility in Janabiyah, Northern, BH . This is an on-site role critical to ensuring the integrity and safety of their products.
The Senior Pharmaceutical Quality Control Analyst will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products. This includes utilizing advanced analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. You will meticulously analyze test results, interpret data, and compare them against established specifications and regulatory guidelines (e.g., GMP, ICH). Accurate and timely documentation of all testing activities, results, and deviations in compliance with Good Manufacturing Practices (GMP) is a core function.
Key responsibilities include developing and validating analytical methods, troubleshooting equipment issues, and participating in quality investigations. You will be instrumental in maintaining laboratory equipment, ensuring calibration, and managing laboratory supplies. The Senior QC Analyst will also be involved in preparing Certificates of Analysis (CoA) and contributing to regulatory submissions and inspections. Providing training and technical guidance to junior laboratory staff will be an important aspect of this role. Maintaining a safe laboratory environment and adhering to all safety protocols are essential.
Required Qualifications:
This is an excellent opportunity for a dedicated and skilled analyst to contribute to the development and manufacturing of essential pharmaceutical products in a dynamic and growth-oriented company. If you are passionate about quality and possess the required expertise, we encourage you to apply.
The Senior Pharmaceutical Quality Control Analyst will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products. This includes utilizing advanced analytical instrumentation such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. You will meticulously analyze test results, interpret data, and compare them against established specifications and regulatory guidelines (e.g., GMP, ICH). Accurate and timely documentation of all testing activities, results, and deviations in compliance with Good Manufacturing Practices (GMP) is a core function.
Key responsibilities include developing and validating analytical methods, troubleshooting equipment issues, and participating in quality investigations. You will be instrumental in maintaining laboratory equipment, ensuring calibration, and managing laboratory supplies. The Senior QC Analyst will also be involved in preparing Certificates of Analysis (CoA) and contributing to regulatory submissions and inspections. Providing training and technical guidance to junior laboratory staff will be an important aspect of this role. Maintaining a safe laboratory environment and adhering to all safety protocols are essential.
Required Qualifications:
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
- A minimum of 5 years of hands-on experience in pharmaceutical quality control or quality assurance.
- Extensive experience with analytical techniques commonly used in the pharmaceutical industry (HPLC, GC, Karl Fischer, FTIR, UV-Vis, Dissolution testing).
- Thorough understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
- Proven ability to perform method validation and troubleshooting.
- Excellent laboratory skills, with meticulous attention to detail and accuracy.
- Strong data analysis and interpretation capabilities.
- Proficiency in LIMS (Laboratory Information Management System) and other relevant software.
- Effective written and verbal communication skills.
- Ability to work independently and collaboratively within a team.
- Commitment to quality, compliance, and continuous improvement.
- Must be willing to work full-time at our Janabiyah, Northern, BH laboratory.
This is an excellent opportunity for a dedicated and skilled analyst to contribute to the development and manufacturing of essential pharmaceutical products in a dynamic and growth-oriented company. If you are passionate about quality and possess the required expertise, we encourage you to apply.
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6
Senior Pharmaceutical Quality Control Analyst (Remote)
00002 Saar, Northern
BHD95000 Annually
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Our client, a leading pharmaceutical organization, is seeking an experienced Senior Pharmaceutical Quality Control Analyst to join their fully remote team. This crucial role involves overseeing and executing quality control testing procedures for pharmaceutical products, ensuring compliance with stringent regulatory standards (e.g., GMP, FDA). The ideal candidate possesses a deep understanding of analytical chemistry, pharmaceutical manufacturing processes, and quality assurance principles. You will be responsible for method development, validation, stability testing, and the accurate documentation of results. This is a remote-first position, demanding meticulous attention to detail, exceptional organizational skills, and the ability to work autonomously with minimal supervision. You will collaborate closely with R&D, manufacturing, and regulatory affairs departments. Responsibilities include:
- Performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products using various analytical techniques (e.g., HPLC, GC, UV-Vis, dissolution testing).
- Developing, validating, and transferring analytical methods according to regulatory guidelines.
- Conducting stability studies and analyzing data to determine product shelf-life.
- Investigating out-of-specification (OOS) results and implementing corrective and preventive actions (CAPAs).
- Maintaining laboratory equipment and ensuring proper calibration and maintenance.
- Documenting all laboratory activities and results accurately in compliance with GMP standards.
- Reviewing and approving analytical data and reports.
- Ensuring adherence to all relevant regulatory requirements and quality standards.
- Collaborating with cross-functional teams to address quality issues and support product development.
- Providing training and mentorship to junior analysts.
- Master's degree or Ph.D. in Chemistry, Pharmaceutical Sciences, or a related field.
- Minimum of 7-10 years of progressive experience in pharmaceutical quality control or analytical development.
- Extensive hands-on experience with common analytical instrumentation (HPLC, GC, MS, etc.).
- Thorough understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
- Proven experience in method development, validation, and transfer.
- Strong knowledge of pharmaceutical manufacturing processes.
- Excellent analytical, problem-solving, and critical-thinking skills.
- Exceptional documentation and report-writing abilities.
- Ability to work independently and manage multiple projects effectively in a remote setting.
- Strong interpersonal and communication skills.
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7
Remote Aviation Regulatory Compliance Specialist
101 Al Daih, Northern
BHD85000 Annually
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We are actively recruiting for a dedicated Remote Aviation Regulatory Compliance Specialist to join our growing team. This is a fully remote position, allowing you to contribute your expertise from anywhere. You will play a critical role in ensuring that our operations and services adhere to all applicable aviation regulations, standards, and guidelines. Responsibilities include staying current with evolving regulatory landscapes, interpreting complex aviation laws, developing and implementing compliance policies and procedures, and conducting internal audits to assess adherence. You will liaise with aviation authorities, prepare compliance reports, and provide guidance to internal teams on regulatory requirements. The ideal candidate will possess a strong understanding of global aviation regulations (e.g., ICAO, FAA, EASA), a keen analytical mind, and exceptional attention to detail. A bachelor's degree in Aviation Management, Law, Public Administration, or a related field is required, with a Master's degree being an advantage. Proven experience in aviation regulatory compliance, ideally within an airline, MRO, or regulatory body, is essential. Excellent written and verbal communication skills are necessary for effective reporting and stakeholder engagement. The ability to work independently, manage your time effectively, and maintain meticulous records is crucial for success in this remote role. This position is vital for maintaining our operational integrity and safety record, ensuring seamless operations that impact aviation activities near Budaiya, Northern, BH and beyond. We are seeking a proactive individual who can anticipate regulatory changes and proactively adapt our strategies.
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8
Aviation Safety Inspector - Regulatory Compliance
900 Al Muharraq
BHD70000 Annually
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Our client, a prominent organization within the aviation sector, is seeking a meticulous and experienced Aviation Safety Inspector to join their team. This critical role is responsible for ensuring compliance with all national and international aviation safety regulations. You will conduct regular inspections of aircraft, airport facilities, and operational procedures to identify potential hazards and ensure adherence to safety standards. The ideal candidate will possess a deep understanding of aviation law, aircraft maintenance, air traffic control procedures, and airport operations. Your responsibilities will include performing detailed audits, investigating safety incidents and accidents, developing corrective action plans, and preparing comprehensive inspection reports. You will work closely with flight crews, maintenance personnel, air traffic controllers, and management to promote a strong safety culture throughout the organization. Strong analytical and problem-solving skills are essential, as is the ability to communicate effectively with diverse stakeholders. A commitment to continuous improvement and a proactive approach to risk management are highly valued. This position requires extensive knowledge of safety management systems (SMS) and a keen eye for detail. You will be instrumental in maintaining the highest levels of safety and operational integrity within the aviation environment. Travel may be required to various sites for inspections and investigations. The role requires adherence to strict protocols and a dedication to upholding aviation safety standards. You will be a key player in ensuring the safety of all flight operations and ground activities, contributing to the overall reputation and reliability of our client's operations. The position is based in Sitra, Capital, BH .
Key Responsibilities:
Key Responsibilities:
- Conduct inspections of aircraft, facilities, and operational procedures to ensure compliance with aviation safety regulations.
- Perform audits of maintenance records, operational manuals, and safety management systems.
- Investigate aviation safety incidents, accidents, and near misses to determine root causes.
- Develop and implement corrective action plans to address identified safety deficiencies.
- Prepare detailed inspection reports and recommendations for safety improvements.
- Collaborate with various aviation stakeholders to promote safety awareness and a proactive safety culture.
- Stay current with national and international aviation safety standards and regulations.
- Deliver training on aviation safety procedures and policies as required.
- Significant experience in aviation safety, regulation, or a related operational role.
- In-depth knowledge of aviation legislation, standards, and best practices.
- Experience with Safety Management Systems (SMS).
- Strong analytical, investigative, and reporting skills.
- Excellent communication and interpersonal abilities.
- Ability to work independently and as part of a team.
- Relevant aviation certifications or licenses are highly desirable.
- Bachelor's degree in Aviation Management, Engineering, or a related field preferred.
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