| Location | Leiden, - None Specified - |
|---|---|
| Business Sector | Pharmaceutical |
| Contact email | |
| Job ref | 26454 |
| Published | about 6 hours ago |
QA Specialist
Leiden Area, Netherlands – Permanent
This role sits within a Quality Assurance team supporting GMP manufacturing activities in a fast-growing, innovative life sciences environment focused on advanced therapies. The position plays a key role in maintaining and strengthening the Quality Management System while supporting operational teams across the organization.
The QA Specialist is responsible for ensuring compliance with GMP and related regulations, supporting quality documentation, audits, supplier qualification, and continuous improvement initiatives. The role has broad exposure across manufacturing, QC, validation, and project activities, contributing directly to high-quality product delivery and patient safety.
MSc in Biotechnology, Chemistry, Biopharmaceutics, or equivalent
Minimum 3 years of experience in a (bio)pharmaceutical environment
At least 1 year of recent experience in Quality Assurance
Strong working knowledge of cGMP, GDP, and EMA (or equivalent) regulations
Hands-on experience with deviations, CAPAs, change control, and quality documentation
Experience reviewing and approving SOPs, batch records, validation/qualification documentation, and risk assessments
Experience in sterile manufacturing environments
Exposure to ATMPs, biologicals, vaccines, injectables, or parenteral products
Experience supporting audits and inspections (internal, supplier, or regulatory)
Supplier qualification and oversight experience
Strong communication and coaching skills
Willingness to travel occasionally for audit-related activities
Start Date: As soon as possible
Contract Duration: Permanent
Location: Leiden Area, Netherlands
Additional: Scale-up environment with strong focus on innovation, quality, and continuous improvement
Interviews and offers can move quickly. Send your CV to Ana Jiménez at a.jimenez@panda-int.com today to secure your spot in the process.