Validation Engineer

Syner-G BioPharma Group

Middletown, United States
Market competitive base salary; annual incentive p...
On-site
Bachelor's degree in mechanical or manufacturing engineering
5-7 years experience in biotech or pharmaceutical industries
Proficiency in autocad and solidworks software
The role combines engineering document reviews, equipment startup support, and process/manufacturing engineering with project management responsibilities

Job Summary

  • The role combines engineering document reviews, equipment startup support, and process/manufacturing engineering with project management responsibilities.
  • Syner-G was honored with BioSpace's prestigious 'Best Places to Work' 2026 award for the third consecutive year.
  • Employees enjoy a market competitive base salary, annual incentive plan, robust benefit offerings, and flexible paid time off programs.

Matching Summary

The role combines engineering document reviews, equipment startup support, and process/manufacturing engineering with project management responsibilities.

Salary

Market competitive base salary; Annual incentive plan; Robust benefit offerings including flexible PTO

Skills & Requirements

Must-have

  • Bachelor's degree in Mechanical or Manufacturing Engineering
  • 5-7 years experience in biotech or pharmaceutical industries
  • Proficiency in AutoCAD and SolidWorks software
  • Experience with GMP, FDA regulations, and risk analysis
  • Hands-on validation of automated production systems

Nice-to-have

  • Knowledge of filling and capping equipment
  • Familiarity with PLCs and HMIs
  • Experience with high-speed fill-finish lines
  • Leadership skills to mentor CQV engineers
  • 3D printing expertise for fixture design

Key Requirements

  • Current work authorization required; no visa sponsorship available
  • Willingness to travel up to 100% for client site projects
  • Strong leadership and project management capabilities

Work Rights

Must have current US work authorization

Tailored Resume

Cover Letter