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To be considered for an interview, please make sure your application is full in line with the job specs as found below.
Key Responsibilities & Qualifications
Polymer chemistry with emphasis on characterization techniques (e.g., DSC, GPC, FT‑IR, rheology, dissolution, etc.).
Design and development of particulate and liquid embolic products.
Experience formulating sustained‑release systems, including hydrogel‑based implants or depots.
Development of drug‑device combination products, especially:
Prefilled / pre‑filled syringe systems
Embolization devices
Proven history of parenteral product development, particularly sterile injectables.
Complete CMC (Chemistry, Manufacturing & Controls) development for drug products, including scale‑up and tech transfer.
Design and execution of formulation‑related feasibility studies, DoE/QbD approaches, and process optimization.
Working knowledge of analytical methods for API and finished‑product characterization (e.g., HPLC/UPLC, GC, KF, particle size, viscosity) and data interpretation.
The start date is ASAP/4th May but we can wait for the right person. The initial contract length is 12 months, with multiple extension options after. The role is based in Limerick and will require 3‑4 days onsite per week, with occasional remote work when project allows. The rate is €40‑50 per hour, depending on experience; expenses will be considered. xcfaprz
If you are interested in the role, please send your latest CV and we will call you to discuss further details.
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Sprachkenntnisse
- English
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