Quality Assurance Specialist

Reposted 5 Hours Ago
Be an Early Applicant
El Omrania El Gharbia, Qesm El Omrania, Giza, EGY
In-Office
Entry level
Pharmaceutical
The Role
Monitor environmental conditions, ensure compliance with GMP requirements, oversee manufacturing operations, review documents, and participate in investigations.
Summary Generated by Built In

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 Quality Assurance Specialist to join our dynamic team.

The ideal candidate will contribute to our mission of enhancing human health and well-being, ensuring that we meet the highest standards of excellence in our industry.

Responsibilities:

  • Monitor environmental conditions (temperature, humidity, pressure differentials) and ensure they comply with GMP requirements across production and warehouse areas
  • Participate in raw material dispensing and verify specifications and calculations as per SOPs
  • Oversee manufacturing and packaging operations to ensure adherence to GMP, SOPs, and data integrity requirements
  • Review batch records and logbooks for completeness, accuracy, and compliance with GDP (Good Documentation Practice)
  • Record and report deviations, non-conformities, and incidents. Participate in root cause investigations and track corrective and preventive actions (CAPA)

Requirements
  • Bachelor's degree in Pharmacy.
  • 0-2 years of relevant experience in a pharmaceutical QA environment
  • Knowledge of cGMP and GDP principles
  • Understanding of CAPA, change control, and quality documentation systems
  • Familiarity with ISO 9001 and safety programs
  • Awareness of validation principles and basic statistical concepts

Skills Required

  • Bachelor's degree in Pharmacy
  • 0-2 years of relevant experience in a pharmaceutical QA environment
  • Knowledge of cGMP and GDP principles
  • Understanding of CAPA, change control, and quality documentation systems
  • Familiarity with ISO 9001 and safety programs
  • Awareness of validation principles and basic statistical concepts
Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

The Company
5,629 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account