Job description
Role Overview:
As a key contributor to the regional manufacturing and supply chain excellence, you will be responsible for driving the implementation, optimization, and ongoing maintenance of manufacturing processes across multiple sites. You will work closely with cross-functional teams and global counterparts to ensure seamless product delivery, regulatory compliance, and operational efficiency across all Telix regions.
Key Responsibilities:
* Lead the design, validation, and continuous improvement of manufacturing processes in full compliance with GMP and GDP standards.
* Manage the end-to-end lifecycle of product transfers and new product introductions (NPI) across Seneffe and Herstal sites.
* Collaborate with QA, R&D, Production, Supply Chain, and Regulatory teams to ensure alignment on timelines, quality, and compliance.
* Act as a central point of contact for internal stakeholders and external partners, including CDMOs and other Telix entities.
* Drive project execution in a matrix environment, managing competing priorities under tight deadlines.
* Support change control, deviation management, and CAPA processes using eQMS and ERP systems.
* Ensure accurate documentation, traceability, and audit readiness across all operational activities.
Required Qualifications:
* Bachelor’s or Master’s degree in Chemical Engineering, Pharmaceutical Sciences, Biotechnology, or a related field.
* Minimum of 5 years of progressive experience in pharmaceutical or medical device manufacturing with strong GMP/GDP compliance background.
* Proven experience in radio-pharmaceuticals is highly advantageous.
* Demonstrated ability to thrive in a matrix organization, manage multiple projects simultaneously, and operate effectively under pressure.
* Experience in ERP systems (e.g., SAP) and eQMS platforms (e.g., MasterControl) is preferred.
* Fluency in English and French (written and spoken) is mandatory.
* Strong proficiency in Microsoft Office Suite (Excel, Word, PowerPoint, Outlook).
* Excellent interpersonal, communication, and stakeholder management skills.
* High level of integrity, attention to detail, and commitment to quality and continuous improvement.
Why joining us?
Rapid growth: Amaris has doubled its workforce in Belgium in two years, providing numerous growth opportunities for employees.
Prestigious projects: Candidates will work with renowned clients in the pharmaceutical, biotechnology, and European institutions sectors on impactful missions.
International environment: An agile and dynamic structure promotes intrapreneurship and meritocracy, with international exposure at the heart of Europe.