QC Specialist
Shannononsitemid
via Personio
About this role
Your mission As QC Specialist, you will be responsible for ensuring continued Good Manufacturing Practice (GMP) – compliant activities within QC to support the manufacture and release of plasmids and gene therapy products. This role will be a part of aiding a GMP facility for the production of gene therapy products. As such, it will involve participating in and providing subject matter expertise in equipment qualification, method transfer and routine in-process and release testing within the QC labs, in addition to other QC-supporting activities. Job Description Major Activities Support Technical transfer of the drug substance dilution to QC Shannon. Bridging study for QC dilutions to compare dilution regime in QC to previous TFF to DS dilution.…
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
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2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Shannon. We weight your proximity and willingness to relocate.
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Free · no card · written explanation included
Skills in this role
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