Deviation Investigator

Job overview

The Deviation Investigator role is onsite in Greenville, NC, with a Monday–Friday schedule from 8 a.m. to 5 p.m. Compensation is not specified. The position is a 12-month W-2 contract with a high possibility of extension depending on performance and business needs. The investigator identifies and examines deviations from procedures, quality standards, and regulatory guidelines. The role supports quality assurance and compliance by determining root causes, documenting findings, and coordinating corrective and preventive actions.

What you'll do

• Identify and document deviations from SOPs, quality standards, and regulatory guidelines
• investigate root causes
• collaborate on corrective and preventive actions
• maintain investigation and CAPA records
• prepare reports for management and regulatory authorities as required
• follow Good Documentation Practices
• support audits and inspections
• analyze trends and contribute to continuous improvement.

What we're looking for

Skills & competencies

deviation investigator

quality assurance

deviation management

capa

cgmp

gdp

regulatory compliance

greenville nc

onsite

monday–friday 8 a.m.–5 p.m.

12-month w-2 contract

possible extension

Work arrangement

• Weekend coverage required

Why this role

The posting seeks regulated-industry or cGMP experience and lists technical writing, analytical, and problem-solving skills. Preferred experience includes biologics, aseptic processes, filling isolators, Six Sigma, electronic documentation systems, GMP, and GLP.

About the employer

Integrated Resources, Inc is hiring for this role. Industry: Semiconductor and Related Device Manufacturing. Sector: 33.