Job Opportunities API

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. Job Summary 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.