Senior Quality Control Professional at Eva Pharma

Giza, Giza, Egypt -

Full Time

Start Date

Immediate

Expiry Date

19 Sep, 26

Salary

0.0

Posted On

21 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

HPLC, GC, Dissolution, UV, GMP, GLP, ICH Guidelines, Method Validation, Root Cause Analysis, CAPA, Data Integrity, Stability Program Management, Laboratory Operations, Team Leadership, Analytical Chemistry, Regulatory Compliance

Industry

Pharmaceutical Manufacturing

Description

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. • 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.

Responsibilities

Manage daily laboratory operations to ensure timely testing of raw materials and finished products in compliance with regulatory standards. Lead investigations into OOS and OOT results while supervising the development and coaching of QC staff.