Start Date
Immediate
Expiry Date
21 Dec, 26
Salary
250000.0
Posted On
22 Sep, 26
Experience
25 year(s) or above
Remote Job
Yes
Telecommute
Yes
Sponsor Visa
Yes
Skills
Industry
Pharmaceutical Manufacturing
Quality Assurance Lead
Job Location : Dubai, United Arab Emirates
Key Responsibilities :
• Direct daily Quality Assurance operations to ensure alignment with GMP, Good Distribution Practice (GDP), and local regulatory standards.
• Manage quality management workflows, including Corrective and Preventive Actions (CAPA), deviations, change controls, and complaint root-cause analyses.
• Author, review, and approve Standard Operating Procedures (SOPs), batch manufacturing records, validation protocols, and technical quality documentation.
• Lead internal, client, and health authority regulatory audits while ensuring prompt resolution of audit findings.
• Collaborate cross-functionally with Production, Quality Control, Engineering, and Warehouse teams to maintain product quality compliance.
• Drive continuous process improvement, quality risk management frameworks, and operational excellence across the plant.
Requirements & Qualifications :
• Education & Experience: Bachelor’s Degree in Pharmacy, Chemistry, Life Sciences, or a related scientific field, paired with at least 5 years of progressive Quality Assurance experience in pharmaceutical manufacturing.
• Technical Mastery: Expertise in QMS frameworks, GMP/GDP regulations, risk management methodologies, validation documentation, and health authority audit management.
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Quality Assurance Lead
Job Location : Dubai, United Arab Emirates
Key Responsibilities :
• Direct daily Quality Assurance operations to ensure alignment with GMP, Good Distribution Practice (GDP), and local regulatory standards.
• Manage quality management workflows, including Corrective and Preventive Actions (CAPA), deviations, change controls, and complaint root-cause analyses.
• Author, review, and approve Standard Operating Procedures (SOPs), batch manufacturing records, validation protocols, and technical quality documentation.
• Lead internal, client, and health authority regulatory audits while ensuring prompt resolution of audit findings.
• Collaborate cross-functionally with Production, Quality Control, Engineering, and Warehouse teams to maintain product quality compliance.
• Drive continuous process improvement, quality risk management frameworks, and operational excellence across the plant.
Requirements & Qualifications :
• Education & Experience: Bachelor’s Degree in Pharmacy, Chemistry, Life Sciences, or a related scientific field, paired with at least 5 years of progressive Quality Assurance experience in pharmaceutical manufacturing.
• Technical Mastery: Expertise in QMS frameworks, GMP/GDP regulations, risk management methodologies, validation documentation, and health authority audit management.
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