Deviation Investigation Specialist (15-Month Contract)

PPG US ProPharma Group, LLC; Raleigh (NC); Hybrid; USD 90,000 - 120,000; Part time

Job summary

ProPharma is seeking deviation writers to support quality control activities for pharmaceutical and biotech clients. You will complete required training, participate in meetings, and clearly communicate progress on deviation records.

You will own records through approval, conduct root cause investigations, and develop CAPAs with effectiveness checks. The role requires experience in Quality Control Laboratories, familiarity with Veeva QMS or similar systems, LabVantage, and strong written

Qualifications

• Background in Quality Control Laboratories.
• Experience with root cause investigation and CAPA creation.
• Excellent communication, technical writing skills, and time management skills.
• Experience with Veeva QMS, MODA, or SmartLab.
• Experience in LabVantage.

Responsibilities

• Complete training on time.
• Be present and engaged at meetings.
• Communicate progress on deviation records clearly.
• Own deviation records through approval.
• Conduct thorough root cause investigation, including process background, event overview, creation of CAPA(s) and effectiveness checks.
• Set up deviation review board when applicable.
• Route deviation records for review and approval.

Skills

Communication skills

Technical writing

Time management

Tools

Veeva QMS

MODA

SmartLab

LabVantage

Job description

ProPharma is seeking deviation writers to support quality control activities for pharmaceutical and biotech clients. You will complete required training, participate in meetings, and clearly communicate progress on deviation records.

You will own records through approval, conduct root cause investigations, and develop CAPAs with effectiveness checks. The role requires experience in Quality Control Laboratories, familiarity with Veeva QMS or similar systems, LabVantage, and strong written