Quality Officer, Biotech GMP | Remote Options

Agomab; Antwerpen; Hybrid; EUR 60,000 - 80,000; Full time

Benefits offered by this job

High impact role

Pioneering therapies in biotech

Collaborative environment

Antwerp-based with remote options

Competitive compensation

Job summary

Agomab is seeking a Quality Officer to join the growing Quality team in Antwerp. You will help maintain and improve the QMS, own document control, and provide practical quality support across the organisation.

In this hands-on role, you will work under the Head of Quality to ensure GMP/GCP compliance, lead internal audits, and support regulatory inspections in a dynamic early-stage biotech environment.

Qualifications

• Bachelor's degree in life sciences or related field is required.
• Minimum of three years' experience in quality within biotech/pharma settings.
• Demonstrated GMP/GCP quality system knowledge with recent training or certification.
• Hands-on experience with electronic quality management systems and maintenance.
• Strong continuous improvement mindset and right-first-time principles.
• Ability to translate quality requirements into practical solutions for a growing biotech.

Responsibilities

• Act as a key Quality contact across Agomab and guide colleagues.
• Support development and maintenance of the QMS including procedures and training.
• Coordinate document control and approve operational documents.
• Facilitate risk management, CAPAs, and change control.
• Plan and conduct internal audits and support external audits.
• Prepare and follow up on management review meetings.
• Support validation and lifecycle management of electronic systems.
• Champion continuous improvement and compliance culture.

Skills

GMP/GCP knowledge

Quality management

Documentation control

Problem solving

Cross-functional collaboration

Education

Bachelor's degree in life sciences

Tools

Electronic QMS

Job description

Agomab is seeking a Quality Officer to join the growing Quality team in Antwerp. You will help maintain and improve the QMS, own document control, and provide practical quality support across the organisation.

In this hands-on role, you will work under the Head of Quality to ensure GMP/GCP compliance, lead internal audits, and support regulatory inspections in a dynamic early-stage biotech environment.