QA Officer

 

Job Title: QA Officer

Location: Netherlands, Oss

Hours: Full-time

 

About Citryll: 

We are an innovative biotech company entering a exciting growth phase. Our mission is to advance cutting-edge science while building a robust, future-ready organization. As we grow, we seek an experienced Sr. Director Finance to architect and lead our finance function—driving operational excellence, compliance, and strategic readiness for future funding and exit opportunities.

 

Why Citryll? 

We believe culture is built through shared experiences and intentional practices. Here’s what makes us unique:

• Science-driven impact: We focus on meaningful patient outcomes and scientific rigor
• Transparency & empowerment: We encourage open dialogue and empower teams to make informed decisions
• Continuous learning: We invest in professional growth and celebrate milestones as a team
• Agility & ambition: We embrace change and strive for excellence in everything we do

 

Role overview:

The QA Officer will support the implementation, maintenance, and execution of the Quality Management System (QMS) to ensure the quality and regulatory compliance of the company’s products, processes, and activities. The QA Officer works closely with the QA Manager and cross-functional teams to ensure that quality standards and regulatory requirements are consistently applied throughout product development, manufacturing, and testing activities.

 

Your responsibilities will include:

• Ensure GxP compliance across internal R&D and external partners (CDMOs, CROs, testing labs) supporting development, manufacturing, and clinical activities
• Maintain and develop the Quality Management System (QMS) including document control, SOPs, records, and training compliance
• Manage deviations, CAPAs, and change control across both internal activities and outsourced operations, including investigations and effectiveness checks
• Provide quality oversight of external suppliers including qualification, quality agreements, audit support, and issue follow-up
• Partner with R&D, clinical, CMC, and external vendors to ensure quality and regulatory expectations are built into development programs

 

What Makes You a Great Fit?

Experience:

• Bachelor’s degree (or higher) in a relevant scientific or quality-related discipline (e.g., Pharmaceutical Sciences, Chemistry, Biology, or related field)
• Experience in quality assurance within the pharmaceutical or biotechnology industry (typically 2–5 years)

Skills:

• Strong attention to detail and a structured approach to work
• Good verbal and written communication skills in English
• Ability to work effectively in cross-functional teams and in a dynamic environment
• Proactive mindset with a willingness to learn and develop within the QA function

Knowledge:

• Working knowledge of GMP, GLP, GCP, and/or relevant regulatory guidelines
• Basic understanding of pharmaceutical development, manufacturing, and testing processes

  

Why join us?

• Build the quality department during a pivotal growth stage in an ambitious science driven biotech scale-up
• Collaborate with passionate scientists, innovators, and business leaders