Join EVA Pharma, a leading pharmaceutical company dedicated to empowering the fight for Health and well-being as a fundamental human right. Recognized and certified as a best place to work, we are committed to fostering a supportive and innovative environment for our team members.
We are seeking a passionate and talented Senior Quality Control Professional to join our dynamic team.
The ideal candidate will play a key role in ensuring the accuracy, compliance, and efficiency of quality control laboratory operations while maintaining the highest quality standards across our products and processes.
Key Responsibilities:
• Manage and oversee daily laboratory operations to ensure timely testing of raw materials, in-process, finished, and stability samples in compliance with regulatory requirements and internal standards.
• Review and approve analytical data, calculations, laboratory documentation, and ensure adherence to approved pharmacopeial and validated methods.
• Supervise method validation, verification, transfer activities, and ensure proper qualification and maintenance of analytical instruments.
• Lead investigations of OOS, OOT, and laboratory deviations, ensuring scientifically sound root cause analysis and implementation of effective CAPAs.
• Ensure compliance with GMP, GLP, data integrity (ALCOA+), and maintain continuous inspection readiness.
• Oversee stability program activities, including execution, trending, and support of shelf-life determination.
• Supervise, coach, and develop QC laboratory staff, ensuring high performance, training compliance, and continuous capability development.
• Collaborate with QA, Production, Regulatory Affairs, and other stakeholders to support investigations, audits, and continuous improvement initiatives.
Requirements
• Bachelor’s degree in Science, Chemistry, or a related scientific field.
• 6–8 years of experience in pharmaceutical Quality Control laboratories.
• 2–3 years of experience in a supervisory or team leadership role.
• Strong hands-on experience with HPLC, GC, Dissolution, UV, and other analytical techniques.
• Strong knowledge of GMP, GLP, ICH guidelines, and regulatory requirements.
• Excellent leadership, communication, and problem-solving skills.
EVA Pharma is dedicated to improving access to affordable, high-quality medicines around the world, focusing on three core pillars: innovation, development and sustainable access. The company leverages cutting-edge technology at two research centers bringing first-of-its-kind capabilities to the Middle East and Africa including mRNA research and development from AI prediction to biological products.
With a 5,000-strong team of professionals, EVA Pharma produces more than one million healthcare products a day at four state-of-the-art manufacturing facilities, which are internationally recognized for innovation, and have been approved by multiple regulatory agencies.
Guided by a relentless drive to ensure sustainable access to pressing yet unmet disease areas, the company’s product portfolio focuses on twelve therapeutic areas: Anti-infectives, metabolic health, bone, neuroscience, oncology, respiratory, gynecology, urology and andrology, pediatrics, ophthalmology, gastrointestinal tract, family medicine to meet both local and international demand.
EVA Pharma is one of the fastest-growing healthcare companies in the Middle East and Africa, with an extensive pan-African presence, while operating in more than 60 countries worldwide.
