Job Title: Quality Assurance Specialist
Location: [Sahab]
Job Summary: We are seeking a dedicated Quality Assurance Specialist to ensure that our products meet the highest standards of safety, efficacy, and quality. The QA Specialist will monitor production processes, implement quality management systems, and ensure compliance with regulatory standards specific to the drug and cosmetics industry.
Key Responsibilities:
1. Quality Control and Compliance:
Conduct inspections and audits of production processes to ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements (FDA, ISO, etc.).
Monitor critical control points, product specifications, and manufacturing protocols to prevent quality deviations.
2. Documentation and Record-Keeping:
Maintain accurate records of QA activities, including batch records, test results, and non-conformance reports.
Review and approve production batch records to ensure they meet regulatory standards.
3. Testing and Validation:
Conduct product testing and stability studies for both drugs and cosmetics to ensure adherence to quality standards.
Collaborate with R&D and production teams to validate new processes and equipment.
4. Process Improvement:
Identify areas for improvement in production processes to enhance product quality and minimize defects.
Lead quality improvement projects, root cause analyses, and corrective/preventive actions (CAPAs).
5. Training and Communication:
Train production staff on quality standards, SOPs, and regulatory requirements.
Act as a liaison between quality, production, and regulatory teams to ensure smooth workflow and alignment on quality objectives.
6. Regulatory Compliance:
Stay updated with relevant regulations and standards in the pharmaceutical and cosmetics industry.
Assist with audits and regulatory inspections, providing documentation and support as required.
Qualifications:
Bachelor’s degree in Quality Assurance, Chemistry, Biology, or a related field.
Minimum 3-5 years of QA experience in a pharmaceutical or cosmetics manufacturing environment.
Strong knowledge of GMP, FDA regulations, and ISO standards applicable to drugs and cosmetics.
Excellent attention to detail and organizational skills.
Strong problem-solving and analytical skills.
Ability to work independently and as part of a team.
Please send your CV on this Email:
[email protected] 
