Your new company

Our client, in Belgium, is a global biotechnology company dedicated to treating and curing life-threatening diseases. They develop cell therapies across a diverse range of technology platforms, including autologous and allogenic chimeric antigen receptor T – cell and NK cell – based immunotherapy. They are committed to improving the lives of patients worldwide at multiple sites and their goal is to reimagine healthcare and to deliver transformative treatments in the fields of oncology and cell therapy.

Your new role

• Conducting thorough investigations within our manufacturing process to ensure timely and safe product releases, adhering to GMP standards and regulatory requirements.
• Collaborating with multidisciplinary teams to identify and resolve root causes of incidents, implementing robust corrective and preventive actions (CAPAs).
• Serving as the primary contact for regulatory agencies during inspections, defending investigation strategies and reports).
• Championing research processes and methodologies, implementing process improvements based on lessons learnt and leading to challenging trend investigations to reduce recurring deviations.
• Liaising with various stakeholders to ensure efficient execution of process validation and production schedules.
• Facilitating seamless knowledge transfer between functions and locations for effective problem-solving.

What you'll need to succeed

• Minimum of 3 years of operational experience in a cGMP environment within the biotech or pharmaceutical industry, preferably in cell and gene therapy.
• Thorough knowledge of cGMP regulations and FDA/EU guidelines related to ATMPs. Excellent scientific writing skills.
• You are fluent in Dutch or English, with strong oral and written communication skills.
• Strong analytical, problem-solving, and relationship-building skills
• Positive, ability to meet critical deadlines in a fast-paced environment, and results-oriented attitude

What you'll get in return

Our client in Belgium is offering contracts directly, so you will sign your contract with them. You will get a job that contributes directly to the well-being of patients with an excellent work-life balance within a supportive and innovative working environment that encourages learning and personal development. Alongside that, you will get the chance to work in a multinational company with an open – ended contract and an attractive salary package, starting from €3,900 gross monthly. Other secondary benefits include additional statutory vacations, meal vouchers, group and hospitalisation insurance, an end-of-year bonus and performance bonus. Candidates must be able to commute to work in Ghent or be willing to relocate to Ghent to be considered for this position.

What you need to do now

Are you interested in this vacancy as an MSAT Investigator Associate? Click 'Apply' and send an up-to-date CV or call Sarah Maher on +31202994881 / sarah.maher@hays.com. If this vacancy is not exactly what you are looking for, but you are looking for a different position, please contact us for a confidential discussion about your career options.