411 Pharmaceutical Qa jobs in the United Kingdom

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• Oversee and manage quality assurance activities related to pharmaceutical manufacturing and product release.
• Ensure compliance with Good Manufacturing Practices (GMP) and other relevant regulatory requirements across all operations.
• Develop, implement, and maintain the company's Quality Management System (QMS).
• Conduct internal audits of manufacturing processes, quality systems, and documentation to identify and address non-compliance.
• Participate in external audits and inspections by regulatory authorities (e.g., MHRA, FDA) and customers.
• Review and approve batch records, validation protocols, and other critical quality documents.
• Investigate deviations, out-of-specification (OOS) results, and customer complaints, implementing effective corrective and preventive actions (CAPAs).
• Manage change control processes and assess the impact of changes on product quality.
• Train personnel on quality assurance principles, GMP, and regulatory compliance.
• Collaborate with cross-functional teams, including manufacturing, R&D, and regulatory affairs, to ensure quality standards are met.
• Stay up-to-date with evolving regulatory guidelines and industry best practices.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Minimum of 5-7 years of experience in Quality Assurance within the pharmaceutical or biotechnology industry.
• In-depth knowledge and practical experience with GMP, GDP, and regulatory guidelines (e.g., ICH, FDA, EMA).
• Proven experience in conducting internal audits and participating in regulatory inspections.
• Strong understanding of pharmaceutical manufacturing processes, quality control, and validation principles.
• Excellent analytical, problem-solving, and decision-making skills.
• Exceptional attention to detail and accuracy.
• Strong written and verbal communication skills, with the ability to present complex information clearly.
• Experience with CAPA and change control systems.
• Ability to work independently and collaboratively within a team environment.

• Develop, implement, and maintain robust Quality Assurance programs and systems.
• Ensure all pharmaceutical products and processes comply with regulatory requirements (GMP, ICH, FDA, etc.).
• Oversee the review and approval of batch records, validation protocols, and other critical quality documents.
• Manage internal and external audits, including inspections by regulatory authorities.
• Lead and mentor the Quality Assurance team, fostering a culture of quality and compliance.
• Investigate deviations, out-of-specifications (OOS), and customer complaints, implementing corrective and preventive actions (CAPAs).
• Conduct risk assessments and implement strategies to mitigate quality-related risks.
• Contribute to the development and lifecycle management of pharmaceutical products.
• Liaise with various departments (Manufacturing, R&D, Regulatory Affairs) to ensure quality standards are met.
• Stay updated on evolving regulatory requirements and industry best practices.

• Bachelor's or Master's degree in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 8 years of experience in pharmaceutical Quality Assurance, with at least 3 years in a management role.
• In-depth knowledge of Good Manufacturing Practices (GMP) and relevant regulatory guidelines.
• Proven experience in managing audits, investigations, and CAPA systems.
• Strong understanding of pharmaceutical product development, manufacturing processes, and quality control.
• Excellent leadership, communication, and interpersonal skills.
• Strong analytical and problem-solving abilities.
• Experience with quality management software systems.
• Ability to work effectively under pressure and manage multiple priorities in a dynamic environment.

• Develop, implement, and maintain the company's Quality Management System (QMS) in compliance with cGMP and other relevant regulatory standards.
• Oversee and participate in the review and approval of batch records, deviation reports, change controls, and CAPA (Corrective and Preventive Actions).
• Conduct internal audits and participate in external regulatory inspections (e.g., FDA, EMA) and customer audits.
• Develop and deliver quality assurance training programs to manufacturing, R&D, and other relevant personnel.
• Monitor manufacturing processes and systems to ensure adherence to established quality standards and procedures.
• Review and approve validation protocols and reports for equipment, processes, and analytical methods.
• Manage supplier quality, including the qualification and auditing of raw material and component suppliers.
• Investigate product quality complaints and deviations, determining root causes and implementing effective corrective actions.
• Stay current with evolving pharmaceutical regulations, industry best practices, and emerging quality trends.
• Provide quality assurance support and guidance to cross-functional teams throughout the product lifecycle.
• Lead and participate in quality risk management activities.
• Contribute to the continuous improvement of quality processes and systems.

• Develop, implement, and maintain robust quality assurance systems and procedures in accordance with GMP, GDP, and other relevant regulatory requirements (e.g., MHRA, FDA).
• Review and approve batch records, deviation reports, change controls, CAPAs, and validation protocols/reports.
• Conduct internal audits and inspections to assess compliance with quality standards and identify areas for improvement.
• Participate in external audits by regulatory agencies and customers, serving as a key point of contact for QA-related inquiries.
• Provide QA oversight for manufacturing, packaging, labelling, and testing operations, ensuring adherence to approved procedures.
• Investigate product quality complaints and deviations, determining root causes and implementing effective corrective and preventive actions.
• Manage and maintain quality documentation, including SOPs, work instructions, and training records.
• Train and mentor junior QA personnel, fostering a strong quality culture throughout the organisation.
• Collaborate with cross-functional departments, including manufacturing, R&D, QC, and regulatory affairs, to resolve quality issues and support product lifecycle management.
• Evaluate and approve suppliers and vendors to ensure the quality of raw materials and services.
• Monitor key quality indicators and trends, reporting findings and recommendations to senior management.
• Stay up-to-date with evolving regulatory requirements and industry best practices in pharmaceutical quality assurance.
• Ensure compliance with environmental, health, and safety regulations in all QA-related activities.

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science discipline. A Master's degree is a plus.
• Minimum of 5-7 years of progressive experience in Quality Assurance within the pharmaceutical or biopharmaceutical industry.
• In-depth knowledge of GMP, GDP, ICH guidelines, and relevant regulatory frameworks.
• Proven experience in auditing, deviation management, change control, and CAPA systems.
• Excellent understanding of pharmaceutical manufacturing processes and quality control principles.
• Strong analytical, problem-solving, and decision-making skills.
• Exceptional attention to detail and commitment to accuracy.
• Outstanding written and verbal communication skills, with the ability to present complex information clearly.
• Ability to work independently and collaboratively within a team environment.
• Proficiency in relevant software applications (e.g., LIMS, ERP systems, MS Office Suite).
• Strong leadership potential and mentoring capabilities.

• Lead the development, implementation, and maintenance of the pharmaceutical Quality Management System (QMS).
• Oversee quality assurance activities for all stages of pharmaceutical product development and manufacturing.
• Conduct internal audits and support external regulatory inspections (e.g., FDA, MHRA).
• Lead and participate in investigations, root cause analysis, and CAPA development for deviations and non-conformances.
• Review and approve critical quality documents, including batch records, validation protocols, and SOPs.
• Assess and manage the quality aspects of third-party suppliers and contract manufacturers.
• Provide expert guidance on GMP, ICH guidelines, and other relevant regulatory requirements.
• Mentor and develop junior QA professionals, fostering a culture of quality excellence.
• Manage change control processes and evaluate their impact on product quality.
• Contribute to product lifecycle management by ensuring ongoing compliance and quality robustness.

• MSc or PhD in Pharmacy, Chemistry, Biology, or a related scientific discipline.
• Minimum of 10 years of experience in pharmaceutical Quality Assurance or Quality Control.
• Extensive knowledge of cGMP, ICH guidelines, and global pharmaceutical regulations.
• Proven experience in leading quality investigations and CAPA management.
• Demonstrated success in managing regulatory inspections and audits.
• Strong understanding of pharmaceutical manufacturing processes and analytical techniques.
• Excellent leadership, communication, and interpersonal skills.
• Proficiency in quality risk management principles.
• Ability to work effectively in a fast-paced, complex regulatory environment.
• Strong analytical and problem-solving capabilities.