Posted 1w ago

Process Development Engineer

@ Validation & Engineering Group
Carolina, North Carolina, United States
OnsiteFull Time
Responsibilities:Supporting IQOQ, Designing inspections, Generating documentation
Requirements Summary:5-7+ years in manufacturing/quality engineering in FDA-regulated environments; knowledge of 21 CFR Part 820, GMP, ISO 13485; background in electrical/ mechanical engineering applied to automated manufacturing; experience with automation/controls, tooling, fixtures, test methods, equipment qualification; proficiency in DOE, FMEA, CAPA, root-cause analysis; experience with new product introductions and process scale-up.
Technical Tools Mentioned:DOE, FMEA, CAPA, Automation, Vision systems, PLC, Servo, Pneumatics, Injection molding, Laser welding, Heat bonding
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Process Development Engineer - Careers At Validation & Engineering Group





























 


 












Careers At Validation & Engineering Group










Current job opportunities are posted here as they become available.


 























 


 





Process Development Engineer






Department:
VEG
Location:
Carolina







Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

  • Process Development Engineer

Description:

The Process Development Engineer supports the development, validation, and implementation of new manufacturing processes. The role involves equipment and process validation, documentation generation, process optimization, and cross-functional technical collaboration.

Requirements:

  • 5�7+ years in manufacturing engineering or quality engineering within an FDA-regulated environment (medical devices, pharma, diagnostics, biotech).
  • Strong working knowledge of 21 CFR Part 820, GMP, and ISO 13485.
  • Electrical and mechanical engineering background applied to automated manufacturing systems.
  • Experience with automation/controls, tooling, fixtures, test method development, and equipment qualification.
  • Proficiency in DOE, FMEA, CAPA, and root-cause investigation.
  • Experience supporting new product introductions and process scale-up.

Responsibilities:

  • Support IQ/OQ/PQ and process performance qualification activities; develop validation protocols, reports, and master validation plans.
  • Design and develop in-process and receiving inspection systems for new components and processes.
  • Generate equipment documentation (evaluations, PM/calibration procedures) and manufacturing instructions.
  • Manage process development projects from concept through implementation; collaborate with cross-functional teams.
  • Apply DOE, PFMEA, and risk analysis to characterize, optimize, and improve manufacturing processes.
  • Work with technologies such as laser welding, heat bonding, injection molding, vision systems, and automation (PLC/servo/pneumatics/sensors).

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.


Excited to build something meaningful together? We look forward to hearing from you.


Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.








 


 

 


 

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