QA/RA Officer
Join a fast-growing European biotech Company!
Want to join a growing company in the biotech industry ?
Do you enjoy structured work while participating in a variety of projects ?
Willing to be part of a company advancing health and improving lives ?
At LaCAR, we are advancing health and improving lives.
LaCAR is looking for a QA/RA Officer to contribute to :
- the development, maintenance, and improvement of the Quality Management System (QMS), effectively supporting the business.
- the compliance to normative and regulatory requirements (ISO13485, IVDR, MDSAP, FDA, or any other country regulations).
The job will cover a whole variety of tasks, including day to day tasks (such as regulatory affairs, documents and records management, batch release,…) as well as projects linked to the company growth and regulatory environment. The QA/RA Officer reports to the QA/RA Manager.
Your Key Responsibilities:
· Manage, monitor and update QMS processes, such as documentation & records management / Non-Conformities / CAPA / Data Analysis / Risk Analysis / Change Controls / Regulatory Watches / Product Registration / Post-Market Surveillance
· Review manufacturing documentation / batch records, and release batch
· Prepare and participate in external, internal and supplier audits
· Participate to Design Review and Validation meetings
· Compile Technical Documentation
· Assure the conformity of the QMS processes with the applicable norms/regulatory requirements
· Assure the products registration in EU and outside EU
· Lead and/or participate in QA/RA projects
· Solicit internal and external stakeholders to complete the QA/RA projects
Who Are We?
LaCAR is a fast-growing biotech company developing, producing, and commercializing CE-IVD diagnostic kits for (pharmaco) genetics and newborn screening. Our headquarters are located in the Liège Science Park (Belgium), and we serve customers worldwide.
Who Are We Looking For?
· Master degree in chemistry, biochemistry, biology, biomedical sciences, or a related field
· Familiar with ISO 13485 and IVDR
· Knowledge of MDSAP and FDA regulations is a plus
· Reliable, motivated and committed to delivering high‑quality work
· organized, rigorous and autonomous
· Proactive approach for problem-solving
· good team spirit and like to work with a team
· Advanced level of English (at least B2) for daily professional communication (oral and written)
Why Join Us?
🧬 A dynamic and stimulating environment in the biotech sector.
🎨 A structured role with varied tasks, ideal for developing your expertise.
📈 The opportunity to join an innovative and fast-growing company.
👨👩👧👦 An enthusiastic team – Collaborative and open-minded in an international environment.
💃 Fun team events & great atmosphere.
✅ Flexible working hours & salary package.
⏲️ Permanent contract (38h/week).
🏞️ Inspiring work environment (HQ Belgium)– Overlooking the woods of Sart-Tilman, with a south-facing terrace for afterwork events.
🍇 Free fruits & 🥣 Free-Soup-Tuesdays.
🚀 If this sounds like you, don’t wait—apply now!
📩 Send your CV to jobs@lacar-mdx.com, with the job title in the subject line. (Do not use Easy Apply!)
JOIN LaCAR AND BE PART OF A GROWING BIOTECH JOURNEY!