618 Quality Assurance Analyst jobs in Bahrain
Senior Quality Assurance Analyst
Posted 4 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, document, and execute comprehensive test plans and test cases for software applications.
- Perform various types of testing, including functional, regression, integration, system, and performance testing.
- Identify, document, and track software defects using bug tracking systems (e.g., Jira).
- Collaborate effectively with software developers, product managers, and other stakeholders to ensure timely resolution of issues.
- Analyze test results and provide detailed reports on software quality and defect trends.
- Contribute to the improvement of QA processes, tools, and methodologies.
- Mentor and guide junior QA analysts, fostering their technical development.
- Participate in requirements review and contribute to testability discussions.
- Stay up-to-date with industry trends and best practices in software quality assurance.
- Ensure that all tested products meet specified quality standards and user requirements.
Qualifications:
- Bachelor's degree in Computer Science, Engineering, or a related field, or equivalent practical experience.
- Minimum of 5 years of experience in software quality assurance and testing.
- Proven expertise in designing and executing manual and automated test cases.
- Experience with bug tracking and test management tools (e.g., Jira, TestRail, Zephyr).
- Strong understanding of software development lifecycle (SDLC) and Agile methodologies.
- Excellent analytical, problem-solving, and critical-thinking skills.
- Outstanding attention to detail and commitment to quality.
- Strong written and verbal communication skills, with the ability to articulate technical issues clearly.
- Ability to work independently and manage time effectively in a remote setting.
- Experience with API testing and basic SQL knowledge is a plus.
Senior Pharmaceutical Quality Assurance Analyst
Posted 2 days ago
Job Viewed
Job Description
The Senior Pharmaceutical Quality Assurance Analyst will be responsible for developing, implementing, and maintaining quality systems and procedures. This includes conducting internal audits, investigating deviations and non-conformances, and implementing corrective and preventive actions (CAPA). You will review and approve batch records, validation protocols, and other critical quality documentation. Collaboration with various departments, including R&D, Manufacturing, and Regulatory Affairs, is essential to ensure a robust quality culture throughout the organization.
Key responsibilities involve monitoring manufacturing processes, analyzing quality control data, and preparing regulatory submissions. You will stay abreast of evolving pharmaceutical regulations and guidelines (e.g., GMP, ICH) and ensure the company's compliance. The ideal candidate will possess strong analytical skills, a meticulous attention to detail, and the ability to lead quality improvement initiatives. Experience in pharmaceutical product development, manufacturing, or a related QA/QC role is required. This position offers a significant opportunity to impact patient safety and contribute to the success of innovative pharmaceutical products.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5-7 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Experience with validation, auditing, and CAPA systems.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to interpret complex technical data and regulatory requirements.
- Proficiency in pharmaceutical quality management software.
Remote Pharmaceutical Quality Assurance Analyst
Posted 4 days ago
Job Viewed
Job Description
Responsibilities:
- Review and approve batch records, validation protocols, and other quality-related documentation.
- Participate in internal and external audits, ensuring compliance with Good Manufacturing Practices (GMP) and other regulatory requirements.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Monitor and analyze quality metrics, identifying areas for improvement.
- Develop and update Standard Operating Procedures (SOPs) and other quality system documents.
- Support regulatory submissions and inspections by preparing necessary documentation.
- Collaborate with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, to resolve quality issues.
- Perform risk assessments to identify potential quality issues and implement mitigation strategies.
- Maintain a strong understanding of current pharmaceutical industry regulations and guidelines.
- Contribute to the development and implementation of a robust quality culture.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 4 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of GMP, FDA regulations, and other relevant pharmaceutical quality standards.
- Proven experience in reviewing batch records and implementing CAPA.
- Strong analytical, problem-solving, and critical thinking skills.
- Excellent written and verbal communication skills, essential for remote collaboration.
- Ability to manage multiple tasks, prioritize effectively, and meet deadlines in a remote environment.
- Proficiency in quality management systems software and standard office applications.
- Experience with validation processes (IQ, OQ, PQ) is a significant advantage.
- Detail-oriented with a commitment to accuracy and compliance.
This remote position offers a fantastic opportunity to contribute your expertise to a leading pharmaceutical organization from the comfort of your home office. If you are passionate about ensuring drug safety and quality, apply today to join our client's dedicated team.
Senior Quality Assurance Analyst - Pharmaceutical
Posted 4 days ago
Job Viewed
Job Description
Senior Pharmaceutical Quality Assurance Analyst
Posted 4 days ago
Job Viewed
Job Description
Key responsibilities will involve:
- Reviewing and approving batch records, validation protocols, and other critical quality documentation.
- Conducting internal audits of manufacturing processes, laboratories, and quality control procedures.
- Investigating deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Participating in regulatory inspections and providing support to audit teams.
- Developing and implementing quality management system improvements.
- Ensuring compliance with all applicable regulatory guidelines, including FDA, EMA, and other international standards.
- Training personnel on quality assurance procedures and regulatory requirements.
- Monitoring quality metrics and preparing reports for management review.
- Collaborating with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, to ensure product quality.
- Assisting in the qualification and validation of new equipment and processes.
- Staying up-to-date with changes in pharmaceutical regulations and industry best practices.
- Evaluating and approving changes to raw materials, components, and finished products.
Remote Senior Quality Assurance Analyst
Posted 4 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop and implement comprehensive test plans, test cases, and test scripts for complex software applications.
- Design and execute manual and automated test scenarios across various platforms and devices.
- Identify, document, and track software defects with clear and detailed bug reports.
- Collaborate with developers and product managers to understand requirements and ensure thorough test coverage.
- Lead and mentor junior QA engineers, providing guidance on testing techniques and best practices.
- Define and implement automation frameworks and tools to improve testing efficiency and effectiveness.
- Conduct regression testing, integration testing, system testing, and user acceptance testing (UAT).
- Analyze test results, generate comprehensive reports, and communicate findings to stakeholders.
- Contribute to the continuous improvement of QA processes and methodologies.
- Participate in Agile/Scrum ceremonies, providing QA perspective and insights.
- Ensure the quality and stability of software releases through rigorous testing.
- Stay up-to-date with the latest QA trends, tools, and technologies.
- Advocate for quality throughout the entire software development lifecycle.
- Perform performance, load, and security testing as needed.
- Review requirements and design documents for testability.
- Bachelor's degree in Computer Science, Engineering, or a related field, or equivalent practical experience.
- Minimum of 5-8 years of experience in software quality assurance and testing.
- Proven experience in developing and executing automated test scripts using tools like Selenium, Cypress, or Playwright.
- Strong knowledge of various testing methodologies (e.g., Agile, Waterfall) and types (e.g., functional, performance, security).
- Experience with bug tracking systems such as Jira.
- Proficiency in one or more programming/scripting languages (e.g., Python, Java, JavaScript).
- Excellent analytical, problem-solving, and critical thinking skills.
- Strong written and verbal communication skills, with the ability to clearly articulate complex issues.
- Ability to work independently and manage multiple priorities effectively in a remote environment.
- Experience in mentoring or leading junior QA team members is highly desirable.
- Familiarity with CI/CD pipelines and concepts is a plus.
- Must have a reliable internet connection and a dedicated, quiet home office environment.
Senior Quality Assurance Analyst, Pharmaceutical Manufacturing
Posted 4 days ago
Job Viewed
Job Description
Key Responsibilities:
- Develop, implement, and maintain Quality Management Systems (QMS) in accordance with cGMP, ICH, and other relevant regulatory guidelines.
- Oversee and conduct routine quality audits of manufacturing processes, raw materials, and finished products.
- Review and approve batch records, validation protocols, and reports for accuracy and compliance.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Collaborate with production, R&D, and regulatory affairs teams to ensure product quality and compliance throughout the product lifecycle.
- Participate in regulatory inspections and provide necessary documentation and support.
- Develop and deliver training programs on quality assurance principles and GMP requirements to relevant personnel.
- Monitor and analyze quality control data to identify trends and areas for improvement.
- Manage change control processes, ensuring proper evaluation and documentation of changes to processes, equipment, or materials.
- Qualify and monitor external suppliers and contract manufacturers for quality compliance.
- Contribute to the continuous improvement of quality processes and systems.
- Ensure all quality-related documentation is meticulously maintained and readily available for review.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. Master's degree is a plus.
- Minimum of 6 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry.
- In-depth knowledge of Good Manufacturing Practices (GMP), regulatory requirements (FDA, EMA, etc.), and quality systems.
- Experience with validation processes (process, cleaning, analytical method validation).
- Strong understanding of pharmaceutical manufacturing processes and quality control testing.
- Excellent analytical, problem-solving, and investigative skills.
- Proficiency in root cause analysis and CAPA development.
- Strong written and verbal communication skills, with the ability to document and present complex information clearly.
- Detail-oriented with a strong commitment to accuracy and compliance.
- Ability to work effectively in a team environment and manage multiple priorities.
- Experience with audits and regulatory inspections is essential.
Be The First To Know
About the latest Quality assurance analyst Jobs in Bahrain !
Remote Senior Pharmaceutical Quality Assurance Analyst
Posted 4 days ago
Job Viewed
Job Description
The ideal candidate will have a proven ability to analyze complex data, interpret regulatory guidelines, and make sound quality decisions. You will collaborate closely with cross-functional teams, including R&D, manufacturing, regulatory affairs, and clinical operations, to ensure quality is embedded at every stage of product development and commercialization. The ability to work independently, manage multiple projects simultaneously, and communicate effectively through virtual channels is paramount. Responsibilities include performing internal audits, participating in external regulatory inspections, investigating deviations and out-of-specification results, and contributing to continuous improvement initiatives. We are looking for a proactive professional who can champion quality culture and drive excellence within a remote-first setting. This role offers a significant opportunity to impact patient safety and product efficacy by upholding the highest quality standards in the pharmaceutical industry.
Responsibilities:
- Review and approve manufacturing batch records, analytical data, and other quality-critical documentation.
- Develop, implement, and maintain quality assurance procedures and systems.
- Ensure compliance with cGMP, ICH guidelines, and other relevant regulatory requirements.
- Participate in internal and external audits and regulatory inspections.
- Investigate deviations, CAPAs, and out-of-specification results.
- Manage change control processes and assess their impact on product quality.
- Develop and execute validation protocols for equipment, processes, and analytical methods.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to resolve quality issues.
- Contribute to continuous improvement efforts and quality risk management.
- Prepare and present quality metrics and reports to senior management.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5 years of experience in pharmaceutical quality assurance or quality control.
- In-depth knowledge of GMP, GLP, and relevant global regulatory requirements (FDA, EMA).
- Experience with quality risk management principles.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills, with the ability to convey complex information clearly.
- Proficiency in electronic quality management systems (eQMS) and data analysis software.
- Ability to work independently and manage time effectively in a remote setting.
- Experience in auditing and inspection readiness is a plus.
Remote Senior Pharmaceutical Quality Assurance Analyst
Posted 4 days ago
Job Viewed
Job Description
This is a remote-first position, allowing you to contribute from anywhere within an approved region. You will conduct thorough reviews of batch records, validation protocols, and other quality-related documentation. Your responsibilities will extend to investigating deviations, implementing corrective and preventive actions (CAPA), and participating in internal and external audits. You will collaborate closely with cross-functional teams, including R&D, manufacturing, and regulatory affairs, to address quality issues and drive continuous improvement. The ability to work autonomously, manage multiple projects simultaneously, and communicate effectively with stakeholders at all levels is crucial for success in this role.
Key Responsibilities:
- Review and approve batch records, stability studies, and other critical quality documents.
- Develop, implement, and maintain quality management systems (QMS) in compliance with global regulatory standards (e.g., FDA, EMA).
- Investigate product quality issues, deviations, and customer complaints, determining root causes and implementing effective CAPA plans.
- Participate in and support regulatory inspections and client audits.
- Develop and execute validation protocols for manufacturing processes, equipment, and analytical methods.
- Conduct risk assessments and implement mitigation strategies to ensure product quality and patient safety.
- Collaborate with R&D, manufacturing, and other departments to resolve quality-related issues and ensure product lifecycle compliance.
- Contribute to the development and improvement of Standard Operating Procedures (SOPs) and other quality documentation.
- Train junior QA personnel and provide mentorship.
- Stay abreast of evolving regulatory requirements and industry best practices.
Qualifications:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5-7 years of experience in pharmaceutical quality assurance or quality control.
- Extensive knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
- Proven experience with QMS implementation, deviation investigations, and CAPA management.
- Strong understanding of validation principles for processes, equipment, and analytical methods.
- Excellent analytical, problem-solving, and critical thinking skills.
- Exceptional written and verbal communication skills, with the ability to clearly articulate complex quality issues.
- Proficiency in using quality management software and electronic data systems.
- Ability to work independently with minimal supervision and manage time effectively in a remote setting.
- Experience with audit preparation and participation is highly desirable.
If you are a dedicated QA professional seeking a challenging remote opportunity within the pharmaceutical sector, apply today to become a vital part of our client's commitment to excellence in drug manufacturing.
Remote Senior Quality Assurance Analyst - FMCG
Posted 4 days ago
Job Viewed
Job Description
Key responsibilities include: developing, implementing, and refining quality assurance policies, procedures, and standards for FMCG products. You will design and execute rigorous testing plans for raw materials, in-process samples, and finished goods, ensuring compliance with internal specifications and external regulatory requirements. Conducting detailed analysis of test results, identifying deviations, and investigating root causes of quality issues are essential. Developing and implementing corrective and preventive actions (CAPAs) to address quality non-conformities is a primary function. You will be responsible for managing and maintaining the quality management system (QMS), ensuring its effectiveness and compliance. Training and mentoring junior QA staff on quality protocols, testing methodologies, and best practices will be part of your role. Collaborating closely with R&D, Production, and Supply Chain teams to integrate quality considerations into product development and manufacturing processes is crucial. Preparing comprehensive quality reports for management, highlighting key metrics, trends, and improvement opportunities, is expected. You will also conduct internal audits and supplier audits to assess compliance and identify areas for enhancement. Staying up-to-date with industry best practices, regulatory changes, and technological advancements in quality assurance within the FMCG sector is vital. Championing a culture of quality throughout the organization will be a key aspect of your leadership.
The ideal candidate will possess a Bachelor's degree in Food Science, Chemistry, Microbiology, Engineering, or a related scientific field. A Master's degree is a plus. A minimum of 5-7 years of progressive experience in quality assurance or quality control within the FMCG industry is required. Demonstrated experience with various quality management systems (e.g., ISO 9001, HACCP, GMP) is essential. Proven ability to develop and implement comprehensive testing protocols and analyze complex data sets is a must. Strong understanding of statistical process control (SPC) and other QA methodologies is required. Excellent analytical, problem-solving, and critical thinking skills are necessary. Outstanding written and verbal communication skills, with the ability to effectively present findings and recommendations to diverse audiences, are crucial. Proficiency in QA software and data analysis tools is expected. Experience with regulatory bodies relevant to the FMCG sector is highly desirable. This remote role is perfect for a seasoned QA professional looking for an impactful opportunity.