Onsite Quality Assurance Auditor — Manufacturing

Catalent; Greenville (NC); On-site; USD 65,000 - 90,000; Full time

Benefits offered by this job

Medical/dental/vision plans

Tuition reimbursement

Paid time off

Wellness programs

Job summary

Catalent’s Greenville, North Carolina site is seeking a Quality Assurance Auditor – Manufacturing to perform routine and non-routine QA tasks in support of internal and external clients and commercial processes. The role emphasizes data integrity, cGMP compliance, and collaboration across Quality Assurance and manufacturing teams.

The position is on-site in Greenville, NC with standard Monday–Friday hours and duties including batch record review, material release, and real-time support for

Qualifications

• Proven ability to ensure data integrity and compliant documentation.
• Experience with cGMP, quality systems, and QA processes.
• Strong attention to detail and cross-functional collaboration.
• Experience reviewing batch records and supporting manufacturing QA activities.

Responsibilities

• Ensure data integrity and accurate documentation of all cGMP activities.
• Advocate for quality standards and maintain a quality culture across the organization.
• Foster open communication within QA and manufacturing teams.
• Support in-process QA checks and release of materials prior to production.
• Review batch records and ensure adherence to SOPs and client requirements.

Skills

Data integrity

Documentation accuracy

Quality mindset

cGMP knowledge

Collaboration

Education

Bachelor's degree in pharmaceutical sciences

Associate degree in a related field

Job description

Catalent’s Greenville, North Carolina site is seeking a Quality Assurance Auditor – Manufacturing to perform routine and non-routine QA tasks in support of internal and external clients and commercial processes. The role emphasizes data integrity, cGMP compliance, and collaboration across Quality Assurance and manufacturing teams.

The position is on-site in Greenville, NC with standard Monday–Friday hours and duties including batch record review, material release, and real-time support for