+30 km
Uren
Opleiding
Dienstverband
Ervaring
Salaris
Datum
Bedrijfstype
Zoek vacatures
Soortgelijke vacatures omgeving Mechelen.
Laad meer vacatures

CMC Lead (Drug Product) Mechelen Panda International

Solliciteer nu
Solliciteer als één van de eersten
Opslaan
Solliciteer nu
Opslaan
Delen

Gevraagd

  • 37 - 40 uur
  • Senior
  • Engels (taal)

Aanbod

  • Tijdelijk contract
 

Vacature in het kort

Mechelen
We are looking for a CMC Leader with expertise in solid oral drug products to guide late-phase development. This role involves leading formulation development, manufacturing, and documentation. You'll be the CMC representative in a cross-functional team. The ideal candidate has strong skills in oral solid formulations, vendor management, and late-stage CMC strategy. This is a full-time contractor role with exciting challenges and opportunities for growth. Join us to make a difference in drug development! Continue reading to see how you can make a difference in our team.
 

Over het bedrijf

Panda International
Bedrijfsprofiel
 

Volledige vacaturetekst

We are seeking a CMC Leader with Drug Product (DP) Solids Expertise to lead late-phase development activities for a solid oral drug product within a small molecule clinical program. This full-time contractor role is based in Mechelen and will run from early September 2025 to March 2026. The selected candidate will oversee formulation development, manufacturing, and documentation activities, while acting as the CMC representative within the cross-functional project team.

This position requires a senior profile with strong technical expertise in oral solid formulations, vendor oversight, and experience driving late-stage CMC strategy and execution.

Practicalities: 

  • Start Date: ASAP 
  • Duration: until March 2026
  • Interview Process: 2 Stages
  • Location: Mechelen,

Key Responsibilities:

  • Represent CMC in the project team
  • Oversee capsule-to-tablet development activities at Patheon
    • Review & finalize outstanding documentation
    • Evaluate and plan further development activities (e.g. scale-up/optimization post rBA GMP campaign)
  • Monitor capsule and tablet stability studies and extend shelf life if required
  • Archive finalized documents in CAESR
  • Respond to Health Authority questions related to the rBA submission
  • Support due diligence activities, if requested

Profile Requirements:

  • Solid experience in CMC and DP combined (solids formulation expertise is essential)
  • Late-stage development exposure
  • Strong hands-on attitude and external vendor management
  • Experience with cross-functional collaboration
  • Workload: Ideally full-time (min. 80%)
Apply to disucss further! 
Vacature opslaan
 Vacature delen
Sluit
Je notitie is succesvol opgeslagen
Voeg een notitie toe aan deze vacature
Opslaan
Sluit
Bedankt, je melding is verstuurd
Rapporteer deze vacature
Leg kort uit waarom je deze vacature rapporteert:
Versturen
Terug naar vacatures
Sluit
Kies 1 of meer
Sluit
Vacature opgeslagen
Klik op het hartje bovenaan de pagina om je opgeslagen vacatures te zien.
Terug naar vacatures
Sluit
Vul een in