562 Pharmaceutical Qa jobs in Bahrain
Pharmaceutical Quality Assurance Specialist
27010 Al Hidd
BHD78000 Annually
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Our client, a leading pharmaceutical manufacturer, is seeking a meticulous and dedicated Pharmaceutical Quality Assurance Specialist to join our team. This role is vital in ensuring that our pharmaceutical products meet the highest standards of quality, safety, and efficacy throughout the manufacturing process. You will be responsible for implementing and maintaining quality management systems, conducting internal audits, reviewing documentation, and ensuring compliance with regulatory requirements such as GMP (Good Manufacturing Practices). Key responsibilities include developing and revising Standard Operating Procedures (SOPs), participating in validation activities, managing deviation investigations and CAPA (Corrective and Preventive Actions), and collaborating with production and quality control teams to resolve quality issues. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, regulatory guidelines, and quality assurance principles. A Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field is required, along with relevant experience in a pharmaceutical QA/QC environment. Experience with quality management software and a keen eye for detail are essential. This hybrid position offers flexibility, with a combination of remote work and on-site responsibilities at our state-of-the-art facilities near Budaiya, Northern, BH . We are looking for a proactive individual committed to upholding the highest quality standards and contributing to the continuous improvement of our manufacturing operations.
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Pharmaceutical Quality Assurance Specialist
10021 Bilad Al Qadeem, Capital
BHD78000 Annually
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We are looking for a diligent and detail-oriented Pharmaceutical Quality Assurance Specialist to join our fully remote team. This critical role involves ensuring compliance with stringent regulatory standards and maintaining the highest quality across our pharmaceutical operations. You will play a key part in upholding the integrity of our products through rigorous quality management processes, all managed from a remote-first perspective.
Key Responsibilities:
Qualifications:
This is an exceptional opportunity for a seasoned QA professional to make a significant contribution to patient safety and product quality, enjoying the flexibility and benefits of a fully remote role. Our client is committed to excellence and innovation in the pharmaceutical sector.
Key Responsibilities:
- Develop, implement, and maintain quality management systems (QMS) in compliance with GMP, GCP, and other relevant regulations.
- Conduct internal audits and inspections to assess compliance and identify areas for improvement.
- Review and approve batch records, validation protocols, and other quality-related documentation.
- Investigate deviations, non-conformances, and customer complaints, implementing corrective and preventive actions (CAPAs).
- Monitor and analyze quality control data to ensure product consistency and safety.
- Participate in external regulatory inspections and audits.
- Develop and deliver quality assurance training programs to relevant personnel.
- Collaborate with R&D, manufacturing, and regulatory affairs teams to ensure seamless quality oversight.
- Stay informed about evolving regulatory requirements and industry best practices.
- Contribute to the continuous improvement of quality processes and systems.
Qualifications:
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 5 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and other relevant pharmaceutical regulations.
- Experience with conducting internal audits and managing CAPA systems.
- Strong understanding of pharmaceutical manufacturing processes and product lifecycle.
- Excellent analytical, problem-solving, and documentation skills.
- Proficiency in quality management software and tools.
- Strong communication and interpersonal skills, essential for effective remote collaboration.
- Ability to work independently, manage time effectively, and prioritize tasks in a remote setting.
- Meticulous attention to detail and commitment to quality and compliance.
This is an exceptional opportunity for a seasoned QA professional to make a significant contribution to patient safety and product quality, enjoying the flexibility and benefits of a fully remote role. Our client is committed to excellence and innovation in the pharmaceutical sector.
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1
Pharmaceutical Quality Assurance Specialist
301 Riffa, Southern
BHD4000 Annually
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Our client, a prominent pharmaceutical company, is seeking a meticulous and detail-oriented Pharmaceutical Quality Assurance Specialist to ensure the highest standards of quality and compliance in all aspects of pharmaceutical manufacturing and development. This role is essential for maintaining product integrity and meeting stringent regulatory requirements. The ideal candidate will have a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field, coupled with proven experience in quality assurance within the pharmaceutical industry. Responsibilities include developing, implementing, and maintaining Quality Management Systems (QMS), ensuring compliance with Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other relevant regulatory guidelines. You will be involved in conducting internal audits, preparing for regulatory inspections, and managing deviations, CAPAs (Corrective and Preventive Actions), and change controls. Reviewing and approving batch records, validation protocols, and other quality-related documentation is a key function. The successful candidate must possess a thorough understanding of pharmaceutical manufacturing processes, quality control testing, and regulatory affairs. Excellent analytical, problem-solving, and documentation skills are required, along with strong communication and interpersonal abilities to work effectively with cross-functional teams, including R&D, manufacturing, and regulatory affairs. Familiarity with quality risk management principles and validation processes (e.g., process validation, equipment qualification) is essential. This role requires a commitment to ensuring product safety and efficacy by upholding rigorous quality standards in our **Riffa, Southern, BH** facility. Join our team and contribute to delivering life-changing medicines.
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2
Pharmaceutical Quality Assurance Specialist
777 Bilad Al Qadeem, Capital
BHD85000 Annually
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Our client is a rapidly growing pharmaceutical company committed to producing high-quality medications. We are looking for a dedicated Pharmaceutical Quality Assurance Specialist to join our team, working remotely to uphold the rigorous standards of our manufacturing processes. This role is crucial for ensuring compliance with all relevant regulatory requirements, including GMP (Good Manufacturing Practices), and maintaining the integrity of our pharmaceutical products. You will be responsible for developing and implementing quality assurance procedures, conducting internal audits, reviewing batch records, and managing deviations and change controls. The ideal candidate will have a strong background in pharmaceutical sciences, quality control, or a related field, with in-depth knowledge of regulatory guidelines. Excellent attention to detail, analytical skills, and strong written and verbal communication abilities are essential. You will collaborate with various departments, including R&D, manufacturing, and regulatory affairs, to ensure a cohesive approach to quality. This position requires an individual who can work independently, manage documentation effectively, and contribute to a culture of continuous improvement within a remote work environment. Join us in ensuring the safety and efficacy of life-saving medications.
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3
Pharmaceutical Quality Assurance Manager
2372 Busaiteen, Muharraq
BHD110000 Annually
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Our client, a prominent pharmaceutical company, is seeking a highly experienced Pharmaceutical Quality Assurance Manager to join their team in **Busaiteen, Muharraq, BH**. This hybrid role combines essential on-site responsibilities with the flexibility of remote work. You will be instrumental in establishing and maintaining robust quality management systems, ensuring compliance with regulatory standards, and overseeing all QA activities within the manufacturing and development processes. The ideal candidate will possess a deep understanding of Good Manufacturing Practices (GMP), regulatory affairs, and quality control within the pharmaceutical industry. Your role will be critical in upholding the integrity and safety of our client's pharmaceutical products.
Key Responsibilities:
Required Qualifications:
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with international regulations (e.g., FDA, EMA, GMP).
- Oversee all Quality Assurance activities, including batch record review, release, deviation management, CAPA, and change control.
- Conduct internal audits and support external audits by regulatory agencies and customers.
- Ensure that all manufacturing processes and product development activities adhere to strict quality standards.
- Manage and train the Quality Assurance team, fostering a culture of quality and compliance.
- Review and approve validation protocols and reports for equipment, processes, and analytical methods.
- Monitor and analyze quality metrics, identify trends, and implement corrective and preventive actions (CAPA).
- Stay updated on evolving regulatory requirements and guidelines in the pharmaceutical industry.
- Collaborate with other departments, including R&D, Manufacturing, and Regulatory Affairs, to ensure seamless quality integration.
- Manage supplier quality agreements and perform supplier audits.
- Investigate customer complaints and product quality issues, implementing appropriate resolutions.
- Promote a proactive quality culture throughout the organization.
Required Qualifications:
- Master's degree or Ph.D. in Pharmacy, Chemistry, Biology, or a related life science field.
- Minimum of 8 years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and other relevant regulatory requirements.
- Proven experience in managing QMS, audits, validation, and regulatory submissions.
- Strong leadership, management, and team-building skills.
- Excellent analytical, problem-solving, and decision-making abilities.
- Exceptional attention to detail and commitment to accuracy.
- Strong written and verbal communication skills, with the ability to communicate effectively with regulatory bodies and senior management.
- Proficiency in quality management software and tools.
- Ability to work effectively in a hybrid environment.
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4
Pharmaceutical Quality Assurance Manager
10401 Al Hidd
BHD110000 Annually
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Our client, a leading pharmaceutical company, is looking for an experienced Pharmaceutical Quality Assurance Manager to lead their QA team. This role offers a hybrid work model, requiring a balance of in-office and remote work, allowing for focused strategic planning and team collaboration. The QA Manager will be responsible for ensuring that all pharmaceutical products meet the highest standards of quality, safety, and efficacy. This includes developing and implementing robust quality management systems, overseeing compliance with regulatory requirements (e.g., GMP, FDA), and managing all quality-related activities, from raw material inspection to finished product release. The ideal candidate will possess a strong background in pharmaceutical quality assurance, excellent leadership skills, and a meticulous attention to detail.
Key Responsibilities:
Key Responsibilities:
- Develop, implement, and maintain the company's Quality Management System (QMS).
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Oversee quality control processes, including testing and release of raw materials, intermediates, and finished products.
- Manage and conduct internal and external audits.
- Review and approve batch records, validation protocols, and reports.
- Investigate deviations, CAPAs (Corrective and Preventive Actions), and customer complaints.
- Lead and mentor the Quality Assurance team.
- Collaborate with R&D, manufacturing, and regulatory affairs departments.
- Contribute to the continuous improvement of quality processes and systems.
- Stay updated on regulatory changes and industry best practices.
- Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
- 7+ years of experience in Quality Assurance within the pharmaceutical industry.
- In-depth knowledge of GMP, ICH guidelines, and regulatory affairs.
- Proven experience in managing QMS and conducting audits.
- Strong leadership, team management, and interpersonal skills.
- Excellent analytical, problem-solving, and decision-making abilities.
- Proficiency in quality management software and documentation practices.
- Strong communication and report-writing skills.
- Ability to balance onsite and remote work effectively.
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5
Pharmaceutical Quality Assurance Specialist
90301 Hamala, Northern
BHD65000 Annually
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Our client is seeking a diligent and detail-oriented Pharmaceutical Quality Assurance Specialist to join their vital team in **Sanad, Capital, BH**. This role is crucial for ensuring that all pharmaceutical products manufactured and distributed meet stringent quality standards and regulatory requirements. You will be responsible for reviewing and approving batch records, implementing quality control procedures, conducting internal audits, and ensuring compliance with Good Manufacturing Practices (GMP) and other relevant regulations. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing processes, quality management systems, and regulatory guidelines set forth by authorities like the FDA and EMA. Key responsibilities include investigating deviations and out-of-specification (OOS) results, implementing corrective and preventive actions (CAPA), managing documentation control, and participating in validation activities for equipment and processes. You will work closely with production, R&D, and regulatory affairs departments to maintain the highest levels of product quality and safety. This is an on-site position requiring meticulous attention to detail and a commitment to upholding compliance. Your expertise will be instrumental in safeguarding patient health and maintaining the company's reputation for excellence in the pharmaceutical industry.
Responsibilities:
Responsibilities:
- Review and approve batch manufacturing records, analytical data, and other quality-related documentation.
- Ensure compliance with cGMP, ICH guidelines, and other applicable regulatory standards.
- Investigate deviations, out-of-specification results, and customer complaints, implementing CAPA as needed.
- Participate in internal and external audits, and assist in regulatory inspections.
- Develop, review, and approve Standard Operating Procedures (SOPs) and other quality documents.
- Manage the change control process for materials, equipment, and processes.
- Conduct validation activities for equipment, processes, and analytical methods.
- Perform incoming material inspections and supplier quality assessments.
- Monitor and analyze quality metrics to identify trends and areas for improvement.
- Train personnel on quality systems and GMP requirements.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related scientific field.
- Minimum of 3 years of experience in Quality Assurance or Quality Control within the pharmaceutical industry.
- Thorough knowledge of cGMP, GDP, and other pharmaceutical regulatory requirements.
- Experience with quality management systems, deviation investigations, and CAPA.
- Proficiency in reviewing batch records and analytical data.
- Strong analytical and problem-solving skills.
- Excellent written and verbal communication skills.
- Ability to work independently and collaboratively in a team environment.
- Detail-oriented with strong organizational skills.
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Pharmaceutical Quality Assurance Specialist
708 Southern, Southern
BHD80000 Annually
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Job Description
Our client is seeking a highly qualified Pharmaceutical Quality Assurance Specialist for a fully remote position. This role is critical in ensuring that our pharmaceutical products meet the highest standards of quality, safety, and efficacy. You will be responsible for developing, implementing, and maintaining quality management systems that comply with regulatory requirements, such as GMP (Good Manufacturing Practices). Your duties will include reviewing and approving batch records, investigating deviations and out-of-specification results, and managing change controls. You will conduct internal audits and support external regulatory inspections, ensuring all documentation is accurate and up-to-date. The Pharmaceutical Quality Assurance Specialist will also collaborate with various departments, including R&D, manufacturing, and regulatory affairs, to ensure quality is embedded throughout the product lifecycle. Responsibilities include identifying areas for process improvement, implementing corrective and preventive actions (CAPA), and contributing to risk management activities. A strong understanding of pharmaceutical manufacturing processes, analytical testing, and regulatory guidelines is essential. Candidates must possess excellent analytical and problem-solving skills, meticulous attention to detail, and strong written and verbal communication abilities. A Bachelor's degree in a relevant scientific field (e.g., Pharmacy, Chemistry, Biology) and a minimum of 3-5 years of experience in pharmaceutical quality assurance are required. This remote role offers the flexibility to contribute to a vital sector from anywhere, playing a key part in bringing life-saving medications to patients.
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7
Pharmaceutical Quality Assurance Specialist
20070 Saar, Northern
BHD78000 Annually
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Our client is seeking a highly knowledgeable Pharmaceutical Quality Assurance Specialist to ensure compliance with regulatory standards and uphold the highest quality benchmarks within their operations in Saar, Northern, BH . This role is vital for maintaining the integrity of pharmaceutical products and processes. The ideal candidate will possess a strong understanding of GMP (Good Manufacturing Practices), regulatory affairs, and quality management systems within the pharmaceutical industry. Responsibilities include developing, implementing, and maintaining quality assurance policies and procedures. You will conduct internal audits, inspect manufacturing processes, and review batch records to ensure adherence to protocols and identify potential deviations. The Specialist will be responsible for investigating quality complaints, non-conformances, and deviations, determining root causes, and implementing corrective and preventive actions (CAPA). You will also contribute to the validation of manufacturing processes, equipment, and analytical methods. This hybrid role allows for both on-site quality oversight and remote document review and analysis. Strong documentation skills are essential for maintaining accurate and comprehensive quality records. The ability to collaborate effectively with production, R&D, and regulatory affairs departments is crucial. You will participate in regulatory inspections and audits from external agencies. Excellent analytical and problem-solving skills are required to address quality issues proactively. A keen eye for detail and a commitment to maintaining the highest standards of pharmaceutical quality are paramount. The successful candidate will play a critical role in ensuring product safety, efficacy, and compliance, contributing to the company's reputation for excellence in the pharmaceutical sector.
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8
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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