Remote Deviation Investigation Specialist

ProPharma Group; United States; Hybrid; USD 65,000 - 90,000; Full time

Job summary

ProPharma Group seeks an experienced Deviation Writer to support deviation events within Quality Control on a 15-month contract starting in Q4 2026. You will join meetings with site representatives, perform investigations, and develop CAPAs with effectiveness checks.

The role emphasizes ownership of deviation records through approval, clear communication, and strong technical writing. QC lab background and QMS familiarity are beneficial.

Qualifications

• Background in Quality Control Laboratories.
• Experience in root-cause investigation and CAPA creation.
• Excellent communication and technical writing skills.
• Time management skills to ensure timely deviation writing and approvals.

Responsibilities

• Completion of training on time.
• Presence at meetings and engagement with site representatives.
• Clear communication of progress on deviation records.
• Ownership of deviation records through approval process.
• Thorough root cause investigation with event background, CAPA creation and effectiveness checks.
• Set up deviation review board when applicable.
• Route deviation records for review and approval.

Skills

Deviation writing

Communication

Technical writing

Time management

Quality Control

Tools

Veeva QMS

MODA

SmartLab

LabVantage

Job description

ProPharma Group seeks an experienced Deviation Writer to support deviation events within Quality Control on a 15-month contract starting in Q4 2026. You will join meetings with site representatives, perform investigations, and develop CAPAs with effectiveness checks.

The role emphasizes ownership of deviation records through approval, clear communication, and strong technical writing. QC lab background and QMS familiarity are beneficial.