#Utopia
UTOPIA is seeking qualified
Quality Assurance Documentation Specialist
to join our team
🔶Qualifications:
• Bachelor’s degree in Pharmacy, Chemistry, or a related field.
• 2-5 years of experience in QA within the pharmaceutical or similar industry.
• Strong knowledge of GMP regulations and quality standards.
• Excellent documentation and organizational skills.
• Proficiency in quality management systems and document control processes.
• Ability to work independently and collaboratively in a team environment.
🔶Key Responsibilities:
• Review and approve batch records, SOPs, and related documents.
• Perform internal audits and inspections to ensure compliance with GMP standards.
• Monitor and analyze quality metrics to identify areas for improvement.
• Participate in investigations of non-conformances and deviations.
• Coordinate with cross-functional teams to implement corrective and preventive actions (CAPAs).
• Ensure timely preparation and submission of regulatory documentation.
• Manage the issuance, distribution, and control of all factory documentation, including:
• Batch manufacturing records (BMRs).
• Standard operating procedures (SOPs).
• Logbooks and cleaning records.
• Validation protocols and reports.
• Training records and forms.
• Maintain and update the document control system to ensure accurate tracking and archiving of all factory records.
• Support the preparation for external audits and regulatory inspections.
• Ensure effective communication with production, warehouse, and quality control teams regarding document changes or updates.
🔶 We Offer:
• Competitive salary and benefits.
• Opportunities for professional growth and development.
• A dynamic and supportive work environment.
🔶Location: -
10th of Ramadan City, Egypt.
🔶If you are interested, please send your updated CV and a cover letter
write title
Quality Assurance Documentation Specialist
in subject to
[email protected]Application Deadline: [20/12/2024]
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