Quality Assurance Auditor I - Night Shift (Onsite)

Catalent; Manassas (VA); On-site; USD 52,000 - 68,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Benefits on day one

Tuition reimbursement

Paid time off + holidays

Job summary

Catalent in Manassas, VA is seeking a Quality Assurance Specialist I to audit production lines, verify equipment, and ensure adherence to SQF, HACCP and FQP standards. This role also serves as alternate cover for QA Specialist II and involves 100% onsite night shift.

You will document deviations, report to QA Supervisor, collaborate with Production and Packaging teams, and maintain FDA/cGMP compliance while supporting dietary supplement quality.

Qualifications

• Must be able to communicate effectively in English, both verbally and in writing.
• High School Diploma (minimum) and ability to read SOPs and Test Methods.
• GMP and Quality systems knowledge.
• Ability to lift up to 50 pounds.
• Detail-oriented with strong analytical skills.

Responsibilities

• Conduct detailed quality audits of production lines to ensure products meet standards.
• Verify equipment such as metal detectors, x-ray machines, and scales.
• Audit operator paperwork for compliance with quality requirements.
• Report deviations to QA Supervisor with complete details.
• Identify and report housekeeping issues requiring attention.
• Document non-compliance areas and ensure corrective actions are implemented.
• Collaborate with Production and Packaging Managers and associates on daily issues.
• Enter and track result data using computer systems.

Skills

English communication

Attention to detail

Independent work

Cross-functional teamwork

Analytical skills

SOP literacy

Education

Bachelor of Science in Food Science or related major

Job description

Catalent in Manassas, VA is seeking a Quality Assurance Specialist I to audit production lines, verify equipment, and ensure adherence to SQF, HACCP and FQP standards. This role also serves as alternate cover for QA Specialist II and involves 100% onsite night shift.

You will document deviations, report to QA Supervisor, collaborate with Production and Packaging teams, and maintain FDA/cGMP compliance while supporting dietary supplement quality.