Deviation Writer

Overview

We’re hiring a deviation writer to join a pharmaceutical manufacturing team in Durham, North Carolina. This full‑time, on‑site role is ideal for an early‑career scientist or engineer with 1–2 years of experience in GMP manufacturing or quality support.

• Write detailed deviation reports, documenting investigations in compliance with GMP standards
• Collaborate with cross‑functional teams (QA, manufacturing, QC, engineering) to gather data and support root cause analysis
• Ensure timely closure of deviations and support CAPA documentation as needed
• Participate in deviation trending and reporting to drive continuous improvement

• Bachelor’s degree in a scientific or engineering or related field
• 1–2 years of experience in the pharmaceutical industry
• Experience writing or supporting GMP deviation investigations preferred
• Packaging experience is a plus
• Quality Control Lab experience is a plus but not required
• Strong analytical and writing skills
• Familiarity with quality systems is a plus

At Process Alliance, we strive to be a better model for how problems are solved, and solutions are delivered. We believe in providing a supportive and inclusive work environment where employees can thrive both personally and professionally. Join our team and be part of a company that is shaping the future of engineering solutions.

Visit our website at  to explore our projects, expertise, and the impact we make in the engineering and consultancy space.

• Medical insurance
• Vision insurance
• 401(k)
• Paid maternity leave
• Paid paternity leave

Process Alliance is an equal opportunity employer. We encourage applications from candidates of all backgrounds and experiences.

Salary: $–$ annually.

Location:

Durham, NC. Current: posted 3 days ago.

Seniority level: Associate

Employment type: Full‑time

Job function: Consulting and Engineering

Industries: Pharmaceutical Manufacturing