QRC Group, Inc

Pharmaceutical

QAinvestigationLead

$85–125k ~AI est. Gurabo, Gurabo, Puerto Rico CONTRACT
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for executive candidates.

The Brief

“QA investigation Lead at QRC Group, Inc. Skills: QA investigations, cGMP, Quality systems. Manage investigation workflows. Track key metrics”

What You'll Achieve.

Enhance investigation efficiency; Enhance compliance; Enhance continuous improvement

Industry & Context.

Pharmaceutical
Problems you'll solve

Root cause analysis; Data-driven decision making

What They're Looking For.

Must Have

Bachelor’s Degree in Sciences, 10+ years of QA experience, knowledge of cGMP, knowledge of quality systems, Proficiency in TrackWise, Proficiency in SAP, Proficiency in MS Office, English and Spanish communication skills

What You'll Do.

Manage investigation workflows

Lead cross-functional meetings

Ensure thorough root cause analysis

Ensure sustainable corrective actions

How You'll Work.

Team & Collaboration

Managing cross-functional teams

Communication Scope

English; Spanish

Full Job Description

QRC Group, LLC is a firm dedicated to offer services to the Pharmaceutical, Medical Devices and Chemical Industries in the validation and regulatory fields. Log on now to our website http://www.qrcgroup.com / to learn more about our services and solutions! QA Investigations Lead with strong expertise in process investigations, capable of managing cross-functional teams, driving data-driven decision making, and establishing performance metrics (KPIs) to enhance investigation efficiency, compliance, and continuous improvement within GMP-regulated environments. The selected candidate will be responsible for managing investigation workflows, tracking key metrics, leading cross-functional meetings, and challenging teams to ensure thorough root cause analysis and sustainable corrective actions. ## Qualifications * Bachelor’s Degree in Sciences * 10+ years of QA experience in the pharmaceutical industry. * Strong knowledge of cGMP and quality systems. * Proficiency in TrackWise, SAP, MS Office. * Excellent communication skills in English and Spanish (speak, understand and write). ## Additional Information All your information will be kept confidential according to EEO guidelines.

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