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Quality Assurance Manager

Barrington James

Greater London

On-site

GBP 80,000 - 100,000

7 days ago
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Job summary

An established industry player is looking for a Quality Assurance Manager to lead their QA team. This role involves ensuring compliance with regulatory standards, overseeing the Quality Management System, and fostering continuous quality improvement. The ideal candidate will have a strong background in cGMP compliance and managerial experience in a QA environment, particularly within the pharmaceutical sector. This is a fantastic opportunity to make a significant impact on quality assurance processes and help drive the company towards excellence in product quality.

Qualifications

  • 5+ years of managerial experience in a QA environment, preferably in pharmaceuticals.
  • Extensive knowledge of cGMP requirements and Quality Assurance functions.

Responsibilities

  • Supervise and mentor the QA team, ensuring compliance with regulatory standards.
  • Oversee the Quality Management System and maintain adherence to cGMP.
  • Conduct internal audits and develop a company-wide cGMP Training Program.

Skills

Written Communication

Verbal Communication

Problem-Solving

Attention to Confidentiality

Education

B.S. in a Science-related field

Job description

Job Title: Quality Assurance Manager

Location: Massachusetts (Onsite)

Job Type: Full-time


Job Description

We are seeking an experienced Quality Assurance Manager to lead and manage our Quality Assurance (QA) team. The ideal candidate will ensure that all quality processes comply with regulatory standards and align with business objectives. This role involves overseeing the Quality Management System (QMS), maintaining compliance with current Good Manufacturing Practices (cGMP), and fostering continuous quality improvement.


Duties and Responsibilities

  1. Supervise and mentor the Quality Assurance (QA) team, including responsibilities for recruitment, training, and performance coaching.
  2. Oversee and manage the Quality Management System (QMS), ensuring adherence to regulatory standards for drug quality, strength, identity, and purity throughout production and storage.
  3. Develop, implement, and maintain Standard Operating Procedures (SOPs) related to quality assurance activities.
  4. Design and implement programs to enhance quality standards and ensure compliance with business and regulatory requirements.
  5. Define and enforce inspection standards within the QA department.
  6. Conduct and manage internal audits to verify compliance with cGMP requirements.
  7. Develop and oversee a company-wide cGMP Training Program.
  8. Lead the Change Control Committee, ensuring proper documentation and approval for facility, equipment, product, and process modifications.
  9. Review and approve operational procedures related to manufacturing, production, testing, and maintenance, including associated documentation.
  10. Ensure proper quality controls are in place and successfully executed during manufacturing operations.
  11. Analyze and address any discrepancies found in production records.
  12. Serve as the QA department's representative in various organizational meetings.
  13. Develop, manage, and monitor the department's annual budget.
  14. Oversee the hiring process and manage personnel changes within the QA department.
  15. Direct and oversee the daily operations of the QA Department.

Qualifications and Experience

  1. Education: B.S. in a Science-related field (Chemistry, Biology, Pharmacy) or equivalent.
  2. Experience: Minimum of 5+ years of managerial experience in a QA environment, preferably in the generics pharmaceutical industry.
  3. Expertise: Extensive knowledge of cGMP requirements and Quality Assurance functions.
  4. Skills: Strong written and verbal communication skills, problem-solving abilities, and attention to confidentiality.

If you are a highly motivated QA professional with leadership experience and a strong background in cGMP compliance, we encourage you to apply.

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