Process Alliance
Company Overview: Process Alliance is a leading engineering consultancy firm dedicated to delivering innovative solutions in engineering, automation, manufacturing services, and medical devices. With a commitment to being a better model of problem solving, we have been at the forefront of providing cutting-edge engineering services to clients across the life science industry. 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.
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
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
~ 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
Visit our website at to explore our projects, expertise, and the impact we make in the engineering and consultancy space.
We encourage applications from candidates of all backgrounds and experiences.