Quality Assurance Lead
Posted 1 day ago
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Quality Assurance Lead
Posted 19 days ago
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Quality Assurance Technician
Posted 21 days ago
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Quality Assurance Manager
Posted 24 days ago
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- Develop, implement, and maintain the company's Quality Management System (QMS).
- Oversee all quality assurance and quality control activities throughout the manufacturing process.
- Establish and monitor quality metrics and KPIs, analyzing data to identify trends and areas for improvement.
- Conduct regular internal audits and inspections to ensure compliance with quality standards and procedures.
- Lead and manage the QA team, providing training, guidance, and performance feedback.
- Investigate product quality issues, root cause analysis, and implement corrective and preventive actions (CAPA).
- Collaborate with production, engineering, and R&D teams to ensure product quality from design to launch.
- Ensure compliance with relevant industry regulations and certifications (e.g., ISO 9001).
- Manage supplier quality by assessing and auditing suppliers' quality systems.
- Prepare quality reports for senior management, highlighting performance, issues, and improvement initiatives.
- Drive a culture of quality throughout the organization.
- Bachelor's degree in Engineering, Science, or a related field.
- Minimum of 6 years of experience in Quality Assurance or Quality Control, with at least 3 years in a management role within manufacturing.
- In-depth knowledge of Quality Management Systems (QMS), ISO 9001, and relevant manufacturing quality standards.
- Strong understanding of statistical process control (SPC) and root cause analysis methodologies.
- Experience with quality auditing and regulatory compliance.
- Excellent leadership, team management, and problem-solving skills.
- Proficiency in quality management software and tools.
- Strong analytical and reporting skills.
- Excellent communication and interpersonal skills.
Pharmaceutical Quality Assurance Manager
Posted 5 days ago
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Senior Quality Assurance Manager
Posted 5 days ago
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Senior Quality Assurance Engineer
Posted 5 days ago
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Responsibilities:
- Develop and implement robust quality assurance plans and procedures for manufacturing processes.
- Conduct rigorous inspections and testing of raw materials, in-process components, and finished goods.
- Analyze quality data to identify trends, root causes of defects, and areas for improvement.
- Lead and participate in internal and external audits to ensure compliance with quality standards (e.g., ISO 9001).
- Develop and deliver training programs on quality control principles and practices to production staff.
- Collaborate with engineering, production, and R&D teams to address quality issues and implement corrective/preventive actions (CAPA).
- Maintain accurate quality records and documentation.
- Stay updated on the latest quality assurance technologies and methodologies.
- Manage and supervise junior QA personnel.
- Champion a culture of quality throughout the organization.
- Bachelor's degree in Engineering (Mechanical, Industrial, or related field) or equivalent experience.
- 5-7 years of experience in quality assurance within a manufacturing environment.
- Proven experience with quality management systems (e.g., ISO 9001, Six Sigma, Lean Manufacturing).
- Strong knowledge of statistical process control (SPC) and analytical tools.
- Excellent problem-solving and root cause analysis skills.
- Proficiency in using metrology equipment and quality inspection tools.
- Strong communication, leadership, and interpersonal skills.
- Detail-oriented with a commitment to accuracy and precision.
- Experience in data analysis and reporting.
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Pharmaceutical Quality Assurance Specialist
Posted 6 days ago
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Key Responsibilities:
- Develop, implement, and maintain Quality Management Systems (QMS) in compliance with regulatory standards.
- Conduct internal audits and inspections of manufacturing processes, documentation, and facilities.
- Review and approve batch records, validation protocols, and other critical quality documents.
- Investigate deviations, out-of-specification (OOS) results, and customer complaints, and implement corrective and preventive actions (CAPAs).
- Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory guidelines.
- Participate in external audits and inspections by regulatory authorities.
- Provide quality assurance training to personnel involved in pharmaceutical manufacturing.
- Monitor key quality metrics and generate reports for management review.
- Contribute to continuous improvement initiatives within the quality assurance department.
- Stay current with evolving regulatory requirements and industry best practices.
- Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. A Master's degree is a plus.
- Minimum of 3-5 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 systems, including document control, CAPA, change control, and deviation management.
- Strong analytical and problem-solving skills.
- Excellent attention to detail and accuracy.
- Effective written and verbal communication skills.
- Ability to work independently and collaboratively in a team environment.
- Proficiency in Microsoft Office Suite and quality management software.
- Experience in auditing and regulatory inspections is highly desirable.
Pharmaceutical Quality Assurance Specialist
Posted 7 days ago
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Key responsibilities will include:
- Developing, implementing, and maintaining quality management systems (QMS) in compliance with regulatory requirements (e.g., GMP, ISO).
- Conducting internal audits and inspections to assess compliance and identify areas for improvement.
- Reviewing and approving batch records, validation protocols, and other quality-related documentation.
- Investigating deviations, out-of-specification (OOS) results, and customer complaints, implementing corrective and preventive actions (CAPA).
- Participating in regulatory inspections and audits by health authorities.
- Collaborating with production, quality control, and R&D departments to ensure quality is integrated throughout the product lifecycle.
- Developing and delivering quality training programs to site personnel.
- Monitoring key quality indicators and preparing quality reports for management.
- Ensuring that all materials and processes used in manufacturing are properly qualified and validated.
- Staying up-to-date with evolving regulatory landscapes and industry best practices.
- Maintaining accurate and organized quality records.
- Contributing to continuous improvement initiatives within the quality department.
The ideal candidate will possess a Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field. A Master's degree or relevant certifications are a plus. We require a minimum of 3 years of experience in quality assurance or quality control within the pharmaceutical or related industry. Strong knowledge of Good Manufacturing Practices (GMP) and other relevant regulatory guidelines is essential. Excellent analytical, problem-solving, and documentation skills are a must. The ability to work effectively in a team environment, communicate clearly with various departments, and manage multiple tasks simultaneously is crucial. We are looking for an individual with high integrity, attention to detail, and a commitment to upholding the highest quality standards.
Quality Assurance Manager - Manufacturing
Posted 8 days ago
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