Jobs · Manufacturing · New Jersey

Process Engineer III

Thermo Fisher Scientific · Ridgefield, NJ · 2 days ago
On-siteManufacturing$99k–$149k/yrFull-time

Schedule

Standard (Mon-Fri)

Working Conditions

  • Able to lift 40 lbs. without assistance
  • Adherence to all Good Manufacturing Practices (GMP) Safety Standards
  • Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc. allowed
  • Laboratory Setting
  • Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
  • Warehouse

About the role

As a Manufacturing Engineer III at Thermo Fisher Scientific, you will optimize production processes, implement new technologies, and drive continuous improvement initiatives. You'll work with cross-functional teams to ensure the efficient manufacture of high-quality products while maintaining compliance with regulatory requirements. This position offers the opportunity to contribute meaningfully by enabling our customers to make the world healthier, cleaner and safer through innovative manufacturing solutions.

You will manage process improvement projects, provide technical expertise for new product introductions, develop and validate manufacturing processes, and implement automation solutions. Working with R&D, Quality, Production, and other departments, you'll optimize existing processes while ensuring consistent product quality and regulatory compliance. Your analytical skills and engineering expertise will help drive cost reductions, improve efficiencies, and enhance manufacturing capabilities across our operations.

Requirements

  • Advanced Degree plus 3 years of experience, or Bachelor's Degree plus 5 years of experience in manufacturing engineering in regulated industries (pharmaceutical, medical device, or similar)
  • Preferred Fields of Study: Engineering (Mechanical, Electrical, Chemical, Industrial or related field)
  • Professional Engineer (PE) license or relevant certifications beneficial
  • Lean Six Sigma certification preferred
  • Strong knowledge of GMP, ISO standards, and regulatory requirements
  • Expertise in process validation, equipment qualification, and change control management
  • Proficient in statistical analysis and continuous improvement methodologies
  • Experience with automation systems, PLCs, and manufacturing control systems
  • Strong project management skills and ability to work with cross-functional teams
  • Demonstrated success implementing process improvements and cost reduction initiatives
  • Experience with CAD software and manufacturing documentation systems
  • Excellent analytical and problem-solving abilities
  • Strong written and verbal communication skills
  • Ability to work effectively in a dynamic manufacturing environment
  • Experience supporting engineers and technicians

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