Specialist QA - Validation, cGMP
Woburnonsitemid
Posted 105mo ago · via Smartrecruiters
About this role
About Engineering Job Title- Specialist QA Location- Woburn, MA Duration - 12 months with possible extension Key Skills - QA Pharma, Bio, biopharma, cGMP, validation, conformance, CAPAs, Change Bio-pharma space / Biologics . M-F onsite • Knowledge in cGMP / GMP manufacturing and technical knowledge in validation of pharmaceutical processes/systems/equipment • Project Management and organizational skills, including ability to follow assignments through to completion Direct: 732-339-3518 - Ext 2065 Qualifications • Bachelor degree in a science or engineering discipline • No less than 5 years of experience in the pharmaceutical environment and validation Additional All your information will be kept confidential according to EEO guidelines.
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
For this role: less
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 Woburn. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
Pulled from the job description. These are the keywords we'll weight when scoring your fit.
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