Quality Assurance Section Head
- Salary
- Not stated
- Level
- Senior
- 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
- Senior Civil Engineer posted Sep 29
- Senior Electrical Engineer posted Jul 13
- Quality Assurance Specialist posted Jul 8
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 Section Head 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.
Key Responsibilities:
- Lead the Quality Assurance activities related to validation for both sterile and non-sterile operations, ensuring all validation processes comply with regulatory and cGMP requirements.
- Ensure the planning, execution, and monitoring of validation activities across manufacturing processes and systems.
- Collaborate with manufacturing, engineering, and technical teams to ensure validated processes are maintained and continuously improved.
- Conduct internal audits and assessments of validation activities, documentation, and systems to ensure compliance and identify areas for improvement.
- Manage and coordinate CAPA (Corrective and Preventive Action) related to validation findings and quality issues, ensuring timely resolution.
- Support technology transfer and new product introduction, ensuring validation requirements are properly implemented.
- Lead training initiatives to enhance staff understanding of validation practices, sterile and non-sterile operations, and cGMP requirements.
Requirements
- Bachelor’s degree in Pharmacy, Chemistry, or a related field.
- 7–8 years of experience in Quality Assurance within the pharmaceutical industry, with strong expertise in validation activities for both sterile and non-sterile operations, including process validation, cleaning validation, and equipment qualification. Good understanding of cGMP and quality systems is required.
- Experience in managing teams and leading audits, strong experience in managing diverse customer requirements, technology transfer projects, and setting timely communication with customers.
- Excellent English, analytical, problem-solving, and communication skills.
- Proven ability to lead diverse teams across multiple geographical regions.
- Solid background in new product project management, technology transfer, and product launches in compliance with EU standards.
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