Quality Assurance Specialist 2, Floor Support

ProKidney • Winston-Salem, NC

9d • Onsite

About The Position

The Quality Assurance (QA) Specialist II supports routine quality assurance operations within classified manufacturing environments, including cleanrooms. Working with moderate supervision, the Specialist applies Good Manufacturing Practices (cGMP) to perform defined QA activities, support real-time manufacturing operations, and ensure documentation accuracy and compliance. The role involves full gowning, continuous on-floor presence, and collaboration with Manufacturing, Quality Control, and Facilities to support manufacturing operations.

This is a full-time onsite position in classified manufacturing environments. Flexibility and overtime may be needed based on business needs. Due to the hands-on, real-time nature of quality activities, the role is not eligible for remote or hybrid work.

Requirements

• Bachelor’s degree in Biotechnology, Biology, Chemistry, or a related field, or an equivalent combination of education and experience.
• Two years of QA experience in a GMP-regulated manufacturing, laboratory, or quality environment.
• Working knowledge of cGMP principles and quality systems.
• Ability to apply defined procedures and exercise judgment within established parameters.
• Strong attention to detail and documentation accuracy.
• Effective organizational, communication, and collaboration skills.
• Ability to perform physical tasks and work in gowning-required environments.
• Must be eligible to work in the United States without the need for work visa or residency sponsorship.

Nice To Haves

• Exposure to aseptic manufacturing.

Responsibilities

• Provide real-time QA support for low-complexity manufacturing and facility activities in classified environments.
• Maintain continuous on-floor presence to support compliance and production activities.
• Perform basic in-process batch record reviews to ensure accuracy and compliance.
• Review routine documentation such as logbooks, equipment use records, and cleaning logs, and follow up on discrepancies.
• Conduct and verify routine line clearance activities using established procedures and checklists.
• Identify and document quality observations; escalate non-routine or higher-risk issues as appropriate.
• Support deviation documentation, investigations, and remediation with guidance.
• Participate in audits, inspections, and cross-functional quality initiatives as assigned.
• Follow all gowning, safety, and cleanroom behavior requirements.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level