Drug Product Expert (M/F/D)
Tasks:
Scientific project management: Overseeing work packages, defining, and analyzing experimental plans
Collaboration with technical and analytical teams: Interacting with external departments and a pilot plant for – trials
Field presence: It is essential that the candidate has hands-on lab experience, though they may also work with the technical team on certain specific tasks
Reporting: Each experience requires a detailed report
Senior: Minimum of 5 to 6 years of hands-on experience, ideally in the development of solid dosage forms (tablets, capsules)
Expertise in GMP (Good Manufacturing Practices) environment
Experience in clinical development phases and commercial support
Seniority is not tied to the number of years of experience but to real field expertise
The candidate must be able to work collaboratively with various teams, including technical and analytical teams.
Qualification:
NCE/Synthetic molecules/small molecules
Oral dosage forms
Requirements:
Start: asap
Duration: 6 months
Capacity: fulltime
Location: Belgium and remote (40%)