Duties & Responsibilities:
Supervising internal audits to verify quality procedures and ensure compliance to current Good Manufacturing Practices (cGMPs), managing investigations conducted to detect nonconformity.
- Supervising internal audits to verify quality procedures and ensure compliance to cGMP
- Managing investigations conducted to detect nonconformity in processes relative to defined quality standards
- Recommending appropriate corrective and preventive actions to deal with detected violations and nonconformities, as well as any potential risk
- Supervising the preparation of inspection documents and reports needed to record and proceed with compliance activities
- Reviewing Complaint Trending Reports and Food & Drug Association (FDA) six system audits
- Participating in the development of Hikma Egypt Compliance function’s work plan; distributing and following up on work activities, projects and programs, monitoring workflow and reviewing work methods and procedures
- Suggesting plans and programs to boost the effectiveness of Hikma Egypt Compliance function
Job Requirements:
- B.Sc. degree in Pharmacy, Science or Equivalent.
- 4-5 years’ proven experience in Quality Compliance role.
- Functional Competencies: Audit, Data Analysis, Documenting & Recording Information, Technical Writing, Quality Assurance & Management.
Job Location:
HIKMA Specialized Pharmaceuticals, Badr City.
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