Deviation & CAPA Quality Investigator

Us Tech Solutions; Greenville (NC); On-site; USD 55,000 - 69,000; Full time

Job summary

US Tech Solutions is seeking a Quality Assurance Deviation Specialist in Greenville, NC. You will identify deviations from SOPs and regulatory guidelines, perform root-cause investigations, and help implement CAPAs in a cGMP environment.

Precise documentation and GDP compliance are essential as you collaborate with cross-functional teams. The contract role runs for 12+ months, with an hourly rate of $40-$50, depending on experience and qualifications.

Qualifications

• Deviations documented per SOPs and GDP guidelines.
• Strong analytical and problem-solving abilities.
• Knowledge of regulatory requirements and GMP/GLP basics.

Responsibilities

• Identify and document deviations from SOPs, quality standards, or regulatory guidelines.
• Conduct root-cause investigations to determine deviations’ sources.
• Collaborate with cross-functional teams to implement CAPAs.
• Maintain records of deviations, investigations, and CAPAs.

Skills

Deviation management

cGMP environment

Regulatory knowledge

Analytical skills

Technical writing

Microsoft Office

Communication skills

Education

Associate or bachelor’s degree in Life Sciences

Tools

Microsoft Office

Job description

US Tech Solutions is seeking a Quality Assurance Deviation Specialist in Greenville, NC. You will identify deviations from SOPs and regulatory guidelines, perform root-cause investigations, and help implement CAPAs in a cGMP environment.

Precise documentation and GDP compliance are essential as you collaborate with cross-functional teams. The contract role runs for 12+ months, with an hourly rate of $40-$50, depending on experience and qualifications.