Chemical Industry

Formulation Engineer

Overijssel NetherlandsOn-siteFreelanceStart date 11/2025
Contact person
Gabriel Torres Feijo
Project ID
2925291
InnovationAsepsisAutomationBusiness Process ImprovementRegulatory ComplianceProcess EngineeringManufacturingMicrotomeMultidisciplinary ApproachParticle Size AnalysisProgrammable Logic ControllersPolymer ChemistryProduction LineQuality ManagementReproducibilitySearch Engine MarketingTechnology TransferImagingMorphology

Description

We are seeking a mid? to senior?level Formulation Engineer to join a specialist team developing advanced sustained?release injectable therapies. The ideal candidate will have direct expertise in polymer?based microsphere technology for controlled drug release - particularly biodegradable systems such as PLGA - but strong backgrounds in long?acting injectable formulations more broadly (depot injections, in?situ forming gels, or implantable delivery systems) will also be highly valued.

Key Responsibilities
  • Lead formulation design, optimisation, and scale?up for sustained?release injectables.
  • Translate lab?scale processes into robust, GMP?compliant manufacturing methods.
  • Collaborate with Process Engineering, QA/QC, and Analytical Development to ensure product quality and regulatory compliance.
  • Troubleshoot formulation and process challenges, driving continuous improvement.
  • Support technology transfer to production lines and external manufacturing partners.


Technical Skills & Techniques
  • Aseptic processes for sterile injectable manufacturing.
  • Process Analytical Technology (PAT) for in?process monitoring and control.
  • Automation with PLCs to ensure reproducibility and efficiency in manufacturing.
  • Coulter Counter Multisizer for precise particle size distribution analysis.
  • SEM microtome for high?resolution imaging and particle morphology assessment.


Requirements
  • Background in microsphere technology or long?acting injectable drug delivery systems.
  • Strong understanding of biodegradable polymers, encapsulation techniques, and release?rate optimisation.
  • Familiarity with GMP manufacturing and regulatory guidelines for sterile injectables.
  • Proven ability to lead projects and influence cross?functional teams.
  • Collaborative mindset and hands?on approach in a technical environment.


We Offer
  • The chance to work on innovative drug delivery systems with global impact.
  • A dynamic, multidisciplinary team environment.
  • Competitive salary and benefits.
  • Immediate start for the right candidate.


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