Company 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!
Job Description
QA Specialist / Deviation Investigator to lead investigations of deviations, non conformances, and quality events within a regulated manufacturing environment.
Key Responsibilities:
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Lead end‑to‑end investigations for deviations and quality events.
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Collect and analyze data, conduct interviews, and review technical documentation.
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Apply structured Root Cause Analysis tools (5 Whys, Fishbone, Fault Tree, etc.).
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Develop and manage effective CAPAs addressing true root causes.
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Prepare clear, compliant investigation reports aligned with GMP/GDP requirements.
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Collaborate with Operations, QA, Engineering, and other cross‑functional teams.
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Facilitate and lead problem‑solving and investigation meetings.
Qualifications
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Minimum 3–5 years of experience in deviation investigations, QA operations, or quality systems in regulated environments.
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Experience with GMP/GDP environments and documentation.
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Proficiency with CAPA methodologies and root‑cause‑analysis tools.
Additional Information
All your information will be kept confidential according to EEO guidelines.
