Process Alliance is hiring: Deviation Writer in Indianapolis
Process Alliance, Indianapolis, IN, United States, 46262
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
- 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
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.