QA Officer: GMP & Vendor Compliance (Biotech)

Byondis BV; Nijmegen; On-site; EUR 60,000 - 75,000; Full time

Benefits offered by this job

Pension scheme

30 days annual leave (full-time)

Company events

Job summary

Byondis BV in Nijmegen, the Netherlands, seeks a QA Officer to support vendor qualification and uphold GMP-compliant processes for first-in-human clinical production. You will manage external partners and ensure training records are accurate, collaborating with cross-functional teams to strengthen the quality system.

The role offers growth in QA, quality systems, and regulatory readiness within a collaborative biopharmaceutical environment.

Qualifications

• Quality mindset and collaborative spirit in a dynamic clinical GMP setting.
• Ability to deliver tasks accurately and on time in a First in Human production environment.
• Good English communication; Dutch language is preferred.

Responsibilities

• Vendor qualification and ongoing vendor management to ensure GMP compliance.
• Maintain training documentation and ensure accuracy of training records.
• Support the robust quality system across development and manufacturing activities.

Skills

Quality mindset

Team player

Attention to detail

Can-do attitude

Excellent communication

Cross-functional collaboration

Independent work

Education

Bachelor in biotechnology related studies, life sciences or equivalent

Tools

Computerized systems

Job description

Byondis BV in Nijmegen, the Netherlands, seeks a QA Officer to support vendor qualification and uphold GMP-compliant processes for first-in-human clinical production. You will manage external partners and ensure training records are accurate, collaborating with cross-functional teams to strengthen the quality system.

The role offers growth in QA, quality systems, and regulatory readiness within a collaborative biopharmaceutical environment.