API Manufacturing Lead: GMP Process Innovator

Trasis; Ans; Sur place; EUR 65 000 - 90 000; Plein temps

Résumé du poste

Trasis seeks a scientifically strong professional to drive API synthesis process implementation and on-site GMP-compliant production support. You will supervise initial production activities, ensure proper execution and documentation, and coordinate with Belgian teams to align practices across sites.

You hold a Master’s or PhD in Pharmacy or Chemistry, have GMP experience, and are fluent in French and English. A hands-on, autonomous, solution-focused mindset is essential.

Qualifications

• Master’s or PhD in Pharmacy or Chemistry required, with organic/chemical process focus.
• GMP experience essential and regulatory awareness mandatory.
• Strong knowledge of analytical techniques such as GC and HPLC.
• Proven ownership, resourcefulness, and ability to drive initiatives.
• Solution-oriented mindset with troubleshooting and operability skills.
• Committed to quality, compliance, and regulatory adherence.
• Hands-on mindset, autonomy, pragmatism, and proactive coordination.
• Fluent in French and English; API synthesis experience is a plus.

Responsabilités

• Contribute to API synthesis process implementation at the US site.
• Supervise initial production activities in GMP-compliant settings.
• Ensure proper execution of production steps and documentation.
• Coordinate on-site operations related to API production and resources.
• Monitor production performance and support technical issue troubleshooting.
• Support material flow management and supply availability.
• Ensure quality, safety, and regulatory compliance on site.
• Coordinate with Belgian teams and support the US Sales process if needed.

Connaissances

GMP experience

Analytical techniques

Coordination & communication

French & English fluency

Formation

Master’s degree in Pharmacy or Chemistry

PhD in Pharmacy or Chemistry

Outils

GC

HPLC

Description du poste

Trasis seeks a scientifically strong professional to drive API synthesis process implementation and on-site GMP-compliant production support. You will supervise initial production activities, ensure proper execution and documentation, and coordinate with Belgian teams to align practices across sites.

You hold a Master’s or PhD in Pharmacy or Chemistry, have GMP experience, and are fluent in French and English. A hands-on, autonomous, solution-focused mindset is essential.