466 Quality Assurance Analyst jobs in Bahrain
Pharmaceutical Quality Assurance Analyst
703 Hamala, Northern
BHD2800 month
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Our client, a leading pharmaceutical company, is seeking a highly meticulous and experienced Pharmaceutical Quality Assurance Analyst. This critical role involves ensuring that all pharmaceutical products and processes meet stringent quality standards and regulatory compliance requirements. You will be responsible for conducting quality checks, reviewing batch records, and participating in audits. The ideal candidate possesses a strong understanding of GMP (Good Manufacturing Practices) and relevant pharmaceutical regulations, along with excellent analytical and problem-solving skills. Your attention to detail and commitment to quality will be paramount in upholding the integrity of our client's products.
Key Responsibilities:
Key Responsibilities:
- Perform quality control tests and analysis on raw materials, in-process samples, and finished products.
- Review and approve batch production records and quality control data.
- Conduct internal audits to ensure compliance with GMP and other regulatory standards.
- Investigate deviations, non-conformances, and out-of-specification results.
- Develop and implement corrective and preventive actions (CAPA).
- Participate in external audits by regulatory agencies and customers.
- Prepare quality assurance reports and documentation.
- Contribute to the continuous improvement of quality systems and processes.
- Stay updated on current pharmaceutical regulations and industry best practices.
- Collaborate with production, R&D, and regulatory affairs teams.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- 3+ years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- Thorough knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
- Experience with analytical testing methods and instrumentation.
- Proficiency in documentation, deviation investigation, and CAPA implementation.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and accuracy.
- Good written and verbal communication skills.
- Ability to work effectively in a team environment.
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0
Senior Pharmaceutical Quality Assurance Analyst
90210 Diplomatic Area
BHD110000 Annually
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Our client is seeking a highly skilled and detail-oriented Senior Pharmaceutical Quality Assurance Analyst to join their distributed team. This is a critical, fully remote role focused on ensuring the highest standards of quality in pharmaceutical product development and manufacturing. You will be responsible for developing, implementing, and maintaining robust quality assurance systems and procedures. Key duties include conducting internal audits, reviewing batch records, investigating deviations and out-of-specification results, and ensuring compliance with GMP (Good Manufacturing Practices) and relevant regulatory guidelines (e.g., FDA, EMA). The ideal candidate will have a strong understanding of pharmaceutical manufacturing processes, quality control testing, and regulatory requirements. You will need excellent analytical and problem-solving skills, with the ability to interpret complex data and identify areas for improvement. This position requires a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field, along with a minimum of 5-7 years of experience in pharmaceutical quality assurance or quality control. Experience with CAPA (Corrective and Preventive Actions) systems and change control processes is essential. You must be proficient in documentation review, risk assessment, and validation protocols. As a remote employee, you will collaborate closely with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to ensure product quality and safety. Strong written and verbal communication skills are crucial for reporting findings and communicating with stakeholders. We are looking for a proactive individual dedicated to upholding the integrity and quality of pharmaceutical products. If you are passionate about patient safety and driving quality excellence in a remote work environment, we invite you to apply.
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1
Senior Quality Assurance Analyst - Pharmaceutical
401 Bilad Al Qadeem, Capital
BHD70000 Annually
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Our client, a reputable pharmaceutical company, is seeking a highly detail-oriented Senior Quality Assurance Analyst to join their team in Salmabad, Northern, BH . This vital role ensures that all pharmaceutical products meet stringent quality standards and regulatory requirements. You will be responsible for developing and implementing QA protocols, conducting inspections and audits, analyzing quality data, and contributing to continuous improvement initiatives within the manufacturing and production environment.
Key Responsibilities:
Key Responsibilities:
- Developing, implementing, and maintaining comprehensive quality assurance programs and procedures.
- Conducting internal audits and inspections of manufacturing processes and facilities.
- Reviewing batch records, analytical data, and validation reports for compliance.
- Identifying quality deviations, investigating root causes, and implementing corrective and preventive actions (CAPA).
- Ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines.
- Collaborating with production, R&D, and regulatory affairs teams to ensure product quality.
- Preparing and presenting quality metrics and reports to management.
- Participating in regulatory inspections and responding to regulatory inquiries.
- Training personnel on quality standards and procedures.
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2
Senior Pharmaceutical Quality Assurance Analyst
700 Zallaq, Southern
BHD75000 Annually
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Our client, a leading pharmaceutical company, is seeking a highly experienced Senior Pharmaceutical Quality Assurance Analyst to join their dynamic team in Zallaq, Southern, BH . This critical role involves ensuring that all manufactured pharmaceutical products meet stringent quality standards and regulatory requirements. The successful candidate will play a key part in maintaining compliance with Good Manufacturing Practices (GMP) and other relevant industry guidelines. This position requires meticulous attention to detail, a strong understanding of pharmaceutical manufacturing processes, and a commitment to quality excellence.
Responsibilities:
Responsibilities:
- Develop, implement, and maintain Quality Assurance systems and procedures in accordance with regulatory requirements (e.g., FDA, EMA, SFDA).
- Conduct thorough reviews of batch records, validation protocols, and deviation reports to ensure compliance.
- Perform internal audits of manufacturing processes, quality control laboratories, and documentation to identify areas for improvement.
- Participate in external audits by regulatory agencies and customers, ensuring readiness and successful outcomes.
- Investigate product quality complaints and deviations, identifying root causes and implementing corrective and preventive actions (CAPA).
- Approve or reject raw materials, in-process materials, and finished products based on established specifications.
- Collaborate with production, R&D, and regulatory affairs teams to ensure quality is built into the product lifecycle.
- Train and mentor junior QA staff on quality systems, GMP principles, and regulatory expectations.
- Manage change control processes, ensuring proper documentation and impact assessment for all changes.
- Monitor key quality metrics and performance indicators, providing regular reports to management.
- Stay current with evolving regulatory landscapes and industry best practices in pharmaceutical quality assurance.
- Contribute to the continuous improvement of quality processes and systems.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biotechnology, or a related life science field.
- A minimum of 5 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and other relevant pharmaceutical regulations.
- Experience with quality management systems (QMS), including document control, CAPA, change control, and audits.
- Proficiency in reviewing batch records, validation documents, and analytical data.
- Strong analytical, problem-solving, and decision-making skills.
- Excellent written and verbal communication skills, with the ability to present complex information clearly.
- Meticulous attention to detail and a commitment to accuracy.
- Ability to work independently and as part of a team, managing multiple priorities effectively.
- Experience with pharmaceutical manufacturing processes and quality control testing is highly desirable.
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3
Lead Pharmaceutical Quality Assurance Analyst
10650 Riffa, Southern
BHD85000 Annually
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Our client, a prominent pharmaceutical company, is looking for a Lead Pharmaceutical Quality Assurance Analyst to join their team in Riffa, Southern, BH . This critical role involves ensuring that all pharmaceutical products meet stringent quality standards and regulatory requirements throughout the entire product lifecycle. You will be responsible for developing, implementing, and maintaining comprehensive quality assurance programs and protocols. Your duties will include conducting detailed inspections and audits of manufacturing processes, reviewing batch records, analyzing test results, and identifying areas for improvement. You will collaborate closely with research and development, manufacturing, and regulatory affairs departments to ensure compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant guidelines. This position requires a meticulous approach to detail, strong analytical skills, and a deep understanding of pharmaceutical quality systems. The ideal candidate will have a Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field, coupled with at least 7 years of experience in pharmaceutical quality assurance. Experience with validation processes, CAPA systems, and regulatory submissions is essential. You will also be responsible for mentoring junior QA staff and contributing to the continuous improvement of our quality culture. This is an on-site position, offering an opportunity to work within a state-of-the-art facility and contribute to the development of life-saving medicines.
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4
Junior Pharmaceutical Quality Assurance Analyst
789 Saar, Northern
BHD5500 _annum
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Posted 8 days ago
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Our client, a growing pharmaceutical company, is seeking a motivated and detail-oriented Junior Pharmaceutical Quality Assurance Analyst to join their expanding Quality Assurance department. This entry-level position provides an excellent opportunity to kickstart a career in the highly regulated pharmaceutical industry. The Junior QA Analyst will support the QA team in ensuring that all manufactured products meet stringent quality standards and comply with regulatory guidelines, such as Good Manufacturing Practices (GMP). Your responsibilities will include reviewing and approving batch records, performing line clearance checks, and participating in deviation investigations. You will assist in the maintenance of quality management systems, including document control and change control processes. The role also involves conducting internal audits, monitoring production processes, and identifying areas for improvement. You will work closely with production, quality control, and regulatory affairs departments to ensure a cohesive approach to quality. The ideal candidate will possess a strong understanding of scientific principles, excellent analytical skills, and meticulous attention to detail. A Bachelor's degree in a science-related field (e.g., Pharmacy, Chemistry, Biology) is required. Familiarity with GMP regulations and quality assurance principles is a plus. This position offers significant learning opportunities and career development prospects within a supportive and dynamic work environment. The role is based in **Saar, Northern, BH**. If you are eager to contribute to the development of safe and effective pharmaceutical products, we encourage you to apply.
Responsibilities:
Responsibilities:
- Review and approve batch production records for accuracy and completeness.
- Perform in-process checks and line clearance activities on the manufacturing floor.
- Assist in the investigation of deviations, out-of-specification (OOS) results, and non-conformances.
- Support the maintenance of the Quality Management System (QMS).
- Participate in internal and external audits as required.
- Monitor and verify adherence to GMP regulations and company SOPs.
- Assist in the qualification and validation of equipment and processes.
- Manage document control processes, including document issuance, revision, and archival.
- Prepare quality reports and metrics for management review.
- Collaborate with cross-functional teams to ensure product quality.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
- Strong understanding of GMP, GDP, and other relevant pharmaceutical regulations.
- Excellent analytical and problem-solving skills.
- Meticulous attention to detail and accuracy.
- Proficiency in Microsoft Office Suite, particularly Excel.
- Good written and verbal communication skills.
- Ability to work independently and as part of a team.
- Prior experience in a pharmaceutical QA/QC role is advantageous but not required.
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5
Senior Quality Assurance Analyst - Pharmaceutical
56789 Southern, Southern
BHD75000 Annually
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Posted 11 days ago
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Our client, a rapidly growing pharmaceutical company, is seeking a highly skilled and detail-oriented Senior Quality Assurance Analyst to join their esteemed team in Nuwaidrat, Southern, BH . This critical role involves ensuring that all pharmaceutical products meet stringent quality standards and comply with regulatory requirements. The ideal candidate will possess a strong background in pharmaceutical quality control, excellent analytical abilities, and a thorough understanding of GMP (Good Manufacturing Practices). Responsibilities include developing and implementing QA strategies, performing quality audits, reviewing batch records, and investigating deviations and non-conformances. You will play a vital role in the entire product lifecycle, from raw material testing to finished product release, ensuring the safety and efficacy of all medications. This position requires meticulous attention to detail, proficiency in scientific principles, and the ability to work effectively within a collaborative research and development environment. You will also be responsible for maintaining comprehensive documentation, identifying potential quality risks, and implementing corrective and preventive actions (CAPAs). This is an exceptional opportunity to contribute to the development and production of life-saving medicines and to advance your career in a leading pharmaceutical organization. The candidate will be expected to stay abreast of evolving regulatory landscapes and contribute to the continuous improvement of the company's quality systems, ensuring compliance with international standards.
Responsibilities:
Responsibilities:
- Develop and implement quality assurance plans and procedures.
- Conduct quality audits of manufacturing processes and facilities.
- Review and approve batch records, specifications, and validation documents.
- Investigate deviations, out-of-specification (OOS) results, and non-conformances.
- Implement corrective and preventive actions (CAPAs).
- Ensure compliance with GMP, FDA, and other relevant regulatory guidelines.
- Participate in regulatory inspections and provide necessary documentation.
- Analyze data to identify trends and potential quality issues.
- Contribute to the validation of manufacturing processes and equipment.
- Train personnel on quality assurance procedures and best practices.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. Master's degree preferred.
- Minimum of 5-7 years of experience in pharmaceutical quality assurance.
- In-depth knowledge of GMP, ICH guidelines, and regulatory requirements.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Proficiency in quality management software and systems.
- Experience with regulatory submissions and audits.
- Detail-oriented with strong documentation skills.
- Ability to work independently and as part of a team.
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6
Remote Senior Pharmaceutical Quality Assurance Analyst
BH1-6730 Hamala, Northern
BHD98000 Annually
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Our client is seeking a highly experienced and meticulous Senior Pharmaceutical Quality Assurance Analyst to join their remote operations team. This fully remote position is critical for ensuring the highest standards of quality and compliance within our pharmaceutical product lifecycle. You will be responsible for developing, implementing, and overseeing quality assurance protocols and procedures in accordance with regulatory requirements, including Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Your expertise will be vital in conducting internal audits, reviewing batch records, and investigating deviations or non-conformances to identify root causes and implement corrective and preventive actions (CAPAs). Key responsibilities include developing and validating quality control methods, analyzing manufacturing data, and preparing regulatory submission documentation. You will collaborate closely with R&D, manufacturing, and regulatory affairs departments to ensure product quality and safety from development through to market release. The ideal candidate will possess a strong scientific background in pharmacy, chemistry, or a related life science field, coupled with extensive experience in pharmaceutical quality assurance. Exceptional analytical, problem-solving, and documentation skills are essential. You should be proficient in quality management systems and regulatory guidelines pertinent to the pharmaceutical industry. Excellent communication and interpersonal skills are required to effectively liaise with cross-functional teams and external regulatory bodies. We are looking for a detail-oriented professional who is committed to upholding rigorous quality standards and driving continuous improvement within a remote work environment. This role offers a significant opportunity to impact patient safety and product efficacy, supporting our global initiatives which have a strong connection to the Sanad, Capital, BH region.
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Senior Corporate Counsel, Regulatory Compliance
11701 Seef, Capital
BHD150000 Annually
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Posted 3 days ago
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Our client is seeking a highly motivated and experienced Senior Corporate Counsel specializing in Regulatory Compliance to join their esteemed legal team. This is a fully remote, international position, offering flexibility and the opportunity to work with a dynamic global organization. As a Senior Corporate Counsel, you will play a pivotal role in ensuring our client's operations adhere to all relevant national and international laws and regulations. Your primary responsibilities will include conducting thorough legal research on emerging regulatory landscapes, drafting and implementing comprehensive compliance policies and procedures, and providing expert legal advice on a wide range of compliance matters. You will be instrumental in developing and delivering training programs to employees across various departments on regulatory best practices. This role requires a proactive approach to risk management, identifying potential legal issues before they arise and developing strategies to mitigate them.
The ideal candidate will possess a Juris Doctor (JD) degree from an accredited law school and be admitted to practice law in at least one relevant jurisdiction. A minimum of 7 years of progressive experience in corporate law, with a significant focus on regulatory compliance, financial services regulations, data privacy laws (e.g., GDPR, CCPA), and anti-money laundering (AML) regulations is essential. Proven experience in drafting and negotiating complex commercial contracts and advising on corporate governance matters will be highly regarded. You must demonstrate exceptional analytical skills, a keen attention to detail, and the ability to articulate complex legal concepts clearly and concisely, both in writing and verbally. Proficiency in legal research databases and standard office software is required. This role demands a strong ethical compass, integrity, and the ability to work independently and collaboratively in a fast-paced, remote environment. You will report directly to the General Counsel and work closely with cross-functional teams, including finance, operations, and human resources, to ensure seamless integration of compliance measures throughout the organization.
Responsibilities:
Qualifications:
The ideal candidate will possess a Juris Doctor (JD) degree from an accredited law school and be admitted to practice law in at least one relevant jurisdiction. A minimum of 7 years of progressive experience in corporate law, with a significant focus on regulatory compliance, financial services regulations, data privacy laws (e.g., GDPR, CCPA), and anti-money laundering (AML) regulations is essential. Proven experience in drafting and negotiating complex commercial contracts and advising on corporate governance matters will be highly regarded. You must demonstrate exceptional analytical skills, a keen attention to detail, and the ability to articulate complex legal concepts clearly and concisely, both in writing and verbally. Proficiency in legal research databases and standard office software is required. This role demands a strong ethical compass, integrity, and the ability to work independently and collaboratively in a fast-paced, remote environment. You will report directly to the General Counsel and work closely with cross-functional teams, including finance, operations, and human resources, to ensure seamless integration of compliance measures throughout the organization.
Responsibilities:
- Develop, implement, and maintain robust compliance programs.
- Provide legal guidance on regulatory changes and their impact on the business.
- Conduct internal investigations and respond to regulatory inquiries.
- Draft and review legal documents, policies, and contracts.
- Manage and mentor junior legal staff and external counsel.
- Advise on corporate governance and risk management strategies.
- Stay abreast of all relevant legal and regulatory developments.
Qualifications:
- Juris Doctor (JD) degree from a reputable law school.
- Admission to the bar in a recognized jurisdiction.
- Minimum of 7 years of relevant legal experience.
- Deep understanding of corporate law and regulatory frameworks.
- Excellent research, writing, and communication skills.
- Ability to manage multiple projects simultaneously.
- Proven ability to work effectively in a remote setting.
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8
Senior Aviation Regulatory Compliance Officer
00045 Manama, Capital
BHD105000 Annually
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Posted 3 days ago
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Our client, a fast-growing aviation services company, is seeking a diligent and experienced Senior Aviation Regulatory Compliance Officer to join their team in **Manama, Capital, BH**. This position is responsible for ensuring that all company operations adhere to the stringent regulations set forth by national and international aviation authorities. The Senior Compliance Officer will monitor changes in aviation legislation, assess their impact on the company's procedures, and implement necessary updates. Key responsibilities include developing and maintaining compliance programs, conducting internal audits and assessments, and managing relationships with regulatory bodies. You will be tasked with reviewing operational procedures, training materials, and documentation to ensure ongoing compliance with aviation safety standards, airworthiness requirements, and operational certifications. The ideal candidate will possess a thorough understanding of aviation laws, regulations, and best practices relevant to aircraft operations, maintenance, and air traffic control. This role requires exceptional attention to detail, strong analytical skills, and the ability to interpret complex legal and regulatory texts. The Senior Aviation Regulatory Compliance Officer will also be involved in preparing for external audits and inspections. Excellent communication and interpersonal skills are necessary for collaborating with various departments and external stakeholders. A minimum of 7 years of experience in aviation regulatory compliance, safety management, or a related field is required. A Bachelor's degree in Aviation Management, Law, Public Administration, or a related discipline is essential. Knowledge of relevant aviation regulatory frameworks (e.g., ICAO, EASA, FAA, or GCAA) is mandatory. Experience with compliance management software and conducting internal audits is highly desirable. If you are a proactive compliance professional with a deep commitment to aviation safety and regulatory integrity, we invite you to apply.
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