Senior QA Specialist – CGMP & Compliance (Night Shift)

Cardinal Health; Jackson (MS); On-site; USD 60,000 - 77,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Paid time off

401k savings plan

Health savings account (HSA)

Access to wages before pay day with my

Job summary

Cardinal Health is seeking a Quality Assurance professional to develop and implement a compliant quality system ensuring products and services are reliable, safe, and effective. The role emphasizes investigations, CAPA, and documentation review of batch records, validation, and change controls.

The position is a 40-hour night shift (12:30 am – 8:30 am) with flexibility for production-driven changes; travel within the region is possible, and ISO knowledge is a plus.

Qualifications

• Bachelor’s degree in a related science field or equivalent work experience.
• 2+ years in a related science field; 1–2 years in QA in a regulated environment preferred.
• Experience with cGMP pharmaceutical or medical device environments is a plus.
• Effective written and verbal English communication skills.
• ISO experience is a plus.

Responsibilities

• Review CGMP documentation related to product release, facilities and equipment.
• Establish and report metrics for products and processes as needed by the RQM.
• Ensure site compliance with 21 CFR 212 CGMP requirements.
• Collaborate with operations to drive quality system implementation.
• Perform product release activities and monitor CAPA investigations.
• Conduct aseptic site reviews with operations and document results.

Skills

Quality systems

Root cause analysis

CAPA & problem solving

Investigations

Documentation review

Cross-functional collaboration

Trend analysis

CGMP understanding

Analytical thinking

Education

Bachelor’s degree in related science field

Tools

SAP

Microsoft Excel

Microsoft Word

Microsoft Outlook

Microsoft PowerPoint

Job description

Cardinal Health is seeking a Quality Assurance professional to develop and implement a compliant quality system ensuring products and services are reliable, safe, and effective. The role emphasizes investigations, CAPA, and documentation review of batch records, validation, and change controls.

The position is a 40-hour night shift (12:30 am – 8:30 am) with flexibility for production-driven changes; travel within the region is possible, and ISO knowledge is a plus.