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Manufacturing Process Engineer

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Onsite

Manufacturing Process Engineer

Katalyst CRO

Manufacturing Process Engineer

Skills

Data AnalysisCompliance

6 months ago

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Important information


Contract type:

Freelance / Contract

Location:

Plano, TX, USA

Work mode:

Onsite

Published on:

8 August 2026

What they need


Job Summary

  • Manufacturing Process Engineer with experience in medical device manufacturing, responsible for developing manufacturing processes, performing validations, and ensuring compliance with regulatory requirements in a fast-paced environment.

Roles & Responsibilities:

  • Evaluate process and design alternatives based on Design for Manufacturability principles
  • Ability to work within a team and as an individual contributor in a fast-paced, changing environment
  • Strong verbal and written communication skills with the ability to effectively communicate at multiple levels in the organization
  • Multitasks, prioritizes, and meets deadlines in a timely manner
  • Strong organizational and follow-up skills, with attention to detail
  • Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, company policies, operating procedures, processes, and task assignments

Education & Experience:

  • Bachelor's in Mechanical Engineering or Manufacturing Engineering or equivalent
  • Minimum experience of 4 years in Medical Devices - Manufacturing Engineering
  • Good experience working on Process Validations (IQ, OQ, PQ)
  • Experience developing manufacturing processes and technologies, including process characterization
  • Experience working on PFMEAs
  • Experience performing data analysis using Minitab

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