K
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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