Quality Systems Specialist
Foster Cityonsitemid
Posted 105mo ago · via Smartrecruiters
About this role
The resource should have 2-3 years of prior experience in a regulated cGMP environment . Prior experience in the pharmaceutical /biotech sector is preferred. The resource should have a combination of experience in the Quality Assurance area along with knowledge of Facilities/Utilities design, maintenance, and validation. Additional proficiency in the use of Excel, PowerPoint, Maximo, and TrackWise software is needed. Key job responsibilities are: 1. Development and generation of weekly/monthly QA group metrics. The metrics tracked will be validation document turnaround, Quality System records turnaround, and other group throughput data. 2. Performing first line review of unscheduled Maximo work orders and equipment job plans.…
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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
We compare your skills against the role requirements.
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 Foster City. We weight your proximity and willingness to relocate.
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Free · no card · written explanation included