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.