• Bachelor's Degree in Pharmacy, Chemistry, Biotechnology, or a related field.
• Minimum 5 years experience (with at least 2 years experience in Quality Assurance) within the pharmaceutical industry.
• Strong knowledge and hands‑on experience in Good Manufacturing Practice (GMP) requirements.
• Experience in both Quality Assurance (QA) and Quality Control (QC) functions.
• Proven experience in conducting and managing internal, customer, and regulatory audits.
• Familiarity with quality management systems, documentation control, CAPA, deviation management, and change control.
• Good analytical, problem‑solving, and communication skills.
• Ability to lead a team and work effectively with cross‑functional departments.

Key Responsibilities:

• Oversee all QA and QC activities to ensure compliance with GMP and regulatory requirements.
• Manage quality systems, audits, inspection...