Process Alliance is hiring : Deviation Writer in Indianapolis

Overview

We’re hiring a deviation writer to join a pharmaceutical manufacturing team in Indianapolis, Indiana. 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.

Key Responsibilities

• 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

Qualifications

About Our Culture

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.

Learn more about us

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

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

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