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Scientist – injectable drug product process development

Audenarde
HAYS
Publiée le 10 septembre
Description de l'offre

We are seeking a motivated and scientifically driven professional to join the Injectable Drug Product Process Development team of a well-known Biopharmaceutical company. You will assist to the development of injectable formats such as syringes, cartridges, and vials, supporting projects transitioning into Phase 3 and potentially contributing to early-phase initiatives.

This position offers a dynamic mix of laboratory work, process monitoring, and cross-functional collaboration, with flexibility in remote work and a strong emphasis on scientific rigor and communication.


Key Responsibilities

Laboratory Activities

* Conduct compatibility studies (e.g., film volume, filters, single-use systems)
* Support clinical activities including product preparation and compatibility assessments

Process Development

* Monitor manufacturing processes to ensure product integrity
* Perform sampling, write protocols, and draft scientific reports
* Analyze and interpret data (non-analytical lab work)
* Conduct risk assessments related to scale-up and process changes

Communication & Collaboration

* Work closely with Project Leads and participate in project team meetings
* Maintain regular 1:1s and follow-ups
* Collaborate across departments including Clinical Manufacturing and CMC


Required Qualifications

* 2–3 years of experience in manufacturing or production support
* Familiarity with fill & finish processes (direct or indirect)
* Ability to work independently after onboarding
* Strong scientific critical thinking and problem-solving skills
* Clear, transparent communication style
* High motivation and energy
* Fluent in English (written and spoken)


Preferred Qualifications

* Experience with injectable formats (e.g., syringes)
* Prior collaboration with CMOs
* Understanding of fill & finish steps and their impact on product quality
* Ability to translate project needs into lab protocols
* Experience in writing scientific documentation


Work Environment

* Hybrid work model with a minimum of 40% on-site presence
* Flexibility based on project phase (lab vs. data analysis)


Interested? Please apply on line or call Karin for more information +32 (0)498 17 67 47

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