Deviation Investigator – Quality Assurance Onsite

Adecco US, Inc.; Greenville (NC); Vor Ort; USD 55.000 - 69.000; Vollzeit

Benefits dieser Stelle

Medical benefits

Dental insurance

Vision insurance

Life insurance

Short-term disability

401K plan

Commuter benefits

Employee assistance program

Zusammenfassung

Adecco Healthcare & Life Sciences is seeking a Deviation Investigator to join the Greenville, NC Quality team on a 1-year contract. The role involves investigating deviations, identifying root causes, and implementing CAPAs in a regulated manufacturing setting.

The candidate will maintain GDP-compliant documentation, work cross-functionally with Quality, Manufacturing, Engineering, and Laboratory, and support audits in a fully onsite environment.

Qualifikationen

• Experience in a regulated industry or cGMP environment.
• Experience with deviation management, investigations, root-cause analysis, or CAPA.
• Strong attention to detail and ability to manage multiple investigations and priorities.
• Strong technical writing and documentation skills.

Aufgaben

• Identify, document, and manage deviations from SOPs, quality standards, and regulatory requirements.
• Conduct thorough investigations to determine root cause and contributing factors.
• Gather and evaluate information, documentation, and data to support investigations.
• Collaborate with Quality, Manufacturing, Engineering, Laboratory, and cross-functional teams.
• Support development and implementation of CAPAs.
• Monitor investigation activities for timely completion.

Kenntnisse

Deviation management

Root-cause analysis

CAPA

Technical writing

Collaboration

Regulatory knowledge

Microsoft Word

Microsoft Excel

PowerPoint

Ausbildung

Life Sciences, Engineering, Medical/Healthcare, Quality Management (2+ years)

Tools

Microsoft Word

Microsoft Excel

PowerPoint

Jobbeschreibung

Adecco Healthcare & Life Sciences is seeking a Deviation Investigator to join the Greenville, NC Quality team on a 1-year contract. The role involves investigating deviations, identifying root causes, and implementing CAPAs in a regulated manufacturing setting.

The candidate will maintain GDP-compliant documentation, work cross-functionally with Quality, Manufacturing, Engineering, and Laboratory, and support audits in a fully onsite environment.