Quality Assurance Validation Contractor
Bostononsite
Posted 1mo ago · via Workable
About this role
We are looking for Quality Assurance Validation contractors to join our growing QA Validation group in Boston MA. Positions range from 6 to 12 months. The roles are expected to be onsite in Boston, MA. Responsibilities: Provide QA oversight of CQV activities for the cGMP manufacturing facility and quality control laboratories. Provide QA oversight for periodic review and requalification program. Perform review of CMMS records related to asset management including asset release, database requests, and work orders. Author and perform review of SOPs in Veeva. Review and approve validation protocols and reports (IQ, OQ, PQ, CSV, process validation, cleaning validation). Ensure compliance of validation activities with applicable GMP regulations, industry guidance, and internal SOPs.…
Read the full description on Bio Pharma Consulting JAD Group's site →
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: teams
2
Level fit
We check your title trajectory against the seniority signal of the role.
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 Boston. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
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teams
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