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Upstream Technical Services Specialist, Dublin
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Client:
Quanta part of QCS Staffing
Location:
Dublin, Ireland
Job Category:
Other
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EU work permit required:
Yes
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Job Reference:
b45e6fce32b1
Job Views:
4
Posted:
16.06.2025
Expiry Date:
31.07.2025
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Job Description:
Upstream Technical Services Specialist – Pharmaceuticals - Dublin
Are you looking for the chance to join a life-changing pharmaceutical organization in their mission to continuously drive innovation? We are recruiting for an Upstream Technical Services Specialist.
Located 15 minutes from Dublin Airport and just a short distance from the lively, vibrant, and cultural Irish capital, this leading biopharmaceutical organization features state-of-the-art technology on their unique manufacturing facility.
Responsibilities:
* Upstream (Cell culture focus) including media preparation, large-scale cell culture bulk drug substance manufacturing processes (vial thaw, scale-up, seed reactors, and production bioreactors, harvest centrifugation/clarification).
* Authoring and reviewing process transfer documentation, gap assessments, technical protocols and reports, and process validation documentation, strategy documents.
* Identifying requirements for laboratory studies to support process fit, decisions, or process transfer, and liaising closely with Global Process Development to oversee the design and execution of studies.
* Supporting the introduction of new raw materials and consumables through the generation of materials lists, Bills of Materials, material specifications, and testing requirements.
* Working closely with colleagues in Quality, Supply Chain, and Manufacturing Operations to ensure the availability and release of materials to meet technology transfer and routine manufacturing timelines.
* Identifying and implementing process improvements, e.g., yield enhancement, cycle time reduction.
Required skills and experience:
* Minimum 5+ years’ experience in Technical Services, Process Development, or Manufacturing Support within a biological bulk drug substance manufacturing organization.
* Technical and operational knowledge of multiple unit operations in cell culture processing.
* Comprehensive understanding of cGMP requirements for biopharmaceutical manufacturing.
* Experience with Technology Transfer activities is advantageous.
If this role interests you, please apply now.
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