Job Information
Insight Global Validation Engineer in Raynham, Massachusetts
Job Description
This role is responsible for supporting base business operations and smaller-scale projects while driving process changes and continuous improvement initiatives. The position focuses on reducing scrap, optimizing manufacturing efficiency, and managing non-conformance investigations by implementing effective corrective actions. It also involves supporting quality systems such as CAPA and deviation management, assisting with equipment onboarding—including clean lines, packaging and sealing equipment, lasers, CNC machines, and robotics—and collaborating cross-functionally in a dynamic, fast-paced environment to ensure operational excellence.
We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to HR@insightglobal.com.To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: https://insightglobal.com/workforce-privacy-policy/.
Skills and Requirements
1–2 years of process engineering experience within a GMP-regulated manufacturing environment
Proven ownership of CAPAs and deviation investigations, from drafting through approval
Hands-on experience with process changes, continuous improvement, and scrap reduction activities
Strong background in manufacturing-facing engineering
Familiarity with equipment such as:
Clean lines
Packaging/sealing systems
Lasers
CNC machinery
Robotic programming
Demonstrated autonomous decision-making and ability to lead procedures
Excellent soft skills to navigate cross-functional and high-pressure settings
Strong communication and interpersonal skills. Experience owning and executing IQ, OQ, and PQ validation protocols
Exposure to large utility systems (e.g., water systems) from a validation perspective
Experience with injection molding and/or CNC equipment
Background in pharma or med device industries with emphasis on quality and validation
Scrap validation
Quality NRs
General Process Engineer
Knowledge of Microsoft Office (Word, Excel, PowerPoint, Outlook)
Knowledge of statistical data analysis tools (e.g. Minitab)
Knowledge of Process Excellence/Six Sigma tools and methodologies
Windchill, ETQ, MES