Quality Assurance Specialist
- Salary
- Not stated
- Level
- Junior
- Work type
- Not stated
- Visa
- Not stated
Open. First seen 5 October 2026.
The team: Operations Business Division HIRES STEADILY
This role is one of 15 open in Operations Business Division. 1 was posted in the last 30 days and the oldest in July: a team that hires all year rather than one being built.
WHAT THE TEAM WORKS WITH, ACROSS ITS POSTINGS
AutoCAD (1 of 15), Excel (1 of 15), PLC (1 of 15)
OTHER ROLES ON THIS TEAM
- Senior Maintenance Engineering Professional posted Oct 14
- Vaccine Quality Assurance Section Head posted Sep 6
- Engineering Manager posted Jul 19
- Quality Assurance Section Head posted Jun 29
- Quality Assurance Specialist posted Jun 21
- Car Maintenance Engineering Specialist posted Jun 14
- Senior Maintenance Engineer posted Jun 3
- Quality Assurance Supervisor posted May 12
- Electrical Engineering Professional posted Apr 26
- Senior Quality Assurance Specialist posted Feb 23
- Quality Assurance Specialist posted Nov 30
- Quality Assurance Section Head posted Oct 28
- Senior Civil Engineer posted Sep 29
- Senior Electrical Engineer posted Jul 13
From the team and dates on Eva Pharma's own job board.
About the role
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 Pharmaceutical Sciences or 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.
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