Catalent

pharmaceutical

QualityAssuranceAssociate,Auditing

$0–0k Greenville, North Carolina, United States FULL TIME
The Brief

“Quality Assurance Associate, Auditing at Catalent. Skills: Auditing, Vendor Audits, Risk Assessments. Perform desktop audits and risk assessments for vendors. Support client audits and internal audits”

Industry & Context.

pharmaceutical
Eligibility Requirements

Sit, stand, walk regularly, Occasionally lift up to 15 pounds

What They're Looking For.

Must Have

Bachelor's degree with at least one year of professional experience in a regulated industry, Associate degree with at least two years of professional experience in a regulated industry, Experience writing / revising GMP documents such as audit reports, procedures, protocols, investigations, Three years of experience in a role that requires evaluation, decision making against established procedures and technical writing

Nice to Have

Experience supporting internal and / or external audits

What You'll Do.

Perform desktop audits and risk assessments for vendors

Support client audits and internal audits

schedule and perform Vendor Desktop Audits

Generate Audit Report and Risk

Track CAPAs to completion

Maintain the Approved Supplier List

Support the monitoring of performance and effectiveness of audit program

Ensure all work is performed and documented according to SOPs

Support site client audits

Collaborate with Internal Lead Auditors

Participate in process improvement projects

How You'll Work.

Team & Collaboration

Collaborate with Internal Lead Auditors in the scheduling and execution of internal systems audits

Free ATS check

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