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Senior Quality Control Specialist at Eva Pharma
6th of October, Giza, Egypt -
Full Time

Start Date

Immediate

Expiry Date

13 May, 26

Salary

0.0

Posted On

12 Feb, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Deviation Investigation, Non-conformities Resolution, Root Cause Analysis, Corrective Actions Implementation, Collaboration, Stability Studies, Shelf-life Evaluation, GMP Compliance Monitoring, Internal Audits, External Audits, Documentation, Teamwork, Adaptability

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 Specialist to join our dynamic team. The ideal candidate will play a crucial role in maintaining the highest quality standards in our products and processes. Key Responsibilities: Investigate deviations, non-conformities, and out-of-specification results to identify root causes and implement corrective actions. Collaborate with production and quality assurance teams to ensure timely resolution of quality issues and enhance product quality. Assist in stability studies and evaluate shelf-life data for finished products. Monitor compliance with Good Manufacturing Practices (GMP) and quality standards throughout the production process. Participate in internal and external audits, providing necessary documentation and support. Bachelor’s degree in Science, Biochemistry, or a related field. 2-4 years of experience in quality control or quality assurance within the pharmaceutical or related industry. Ability to work effectively in a team environment and adapt to changing priorities.
Responsibilities
The specialist will investigate deviations and non-conformities to determine root causes and implement corrective actions, while collaborating with production and quality assurance teams to resolve quality issues. They will also assist in stability studies and evaluate shelf-life data for finished products.