Manufacturing QA Auditor — Data Integrity & Compliance

Regulatory Jobs

Greenville (NC)

In loco

USD 70.000 - 90.000

Tempo pieno

14 giorni+

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Vantaggi offerti da questo lavoro

Paid holidays

Tuition reimbursement

Health benefits

Onsite wellness programs

Descrizione del lavoro

Catalent’s Greenville, North Carolina site is a major oral solid dose development and manufacturing campus. This Quality Assurance Auditor – Manufacturing role supports internal and external clients with routine and non-routine QA tasks on site.

Shift: Monday–Friday 8:00am–5:00pm, 100% Onsite in Greenville, NC. Responsibilities include data integrity, driving quality improvements, and ensuring compliance with SOPs and cGMPs across production and packaging operations.

Competenze

Bachelor’s degree with three years of pharmaceutical industry experience, including at least one year in QA.
Associate degree with four years of pharmaceutical experience, including at least two years in QA.
At least one year of batch record review and on-the-floor QA support.

Mansioni

Ensure data integrity through accurate transactions and documentation.
Promote quality standards and a culture of quality and safety across the organization.
Foster open communication within Quality Assurance and across the facility.
Monitor and enforce compliance with SOPs, Quality Agreements, and applicable compendia.
Perform in-process QA checks and review batch records.
Release materials before manufacturing/packaging and provide real-time QA support.
Ensure all work adheres to cGMP requirements.