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Engineer III, Manufacturing

Location Millersburg, Pennsylvania, United States of America Job Id R-01298112 Job Type Full time Category Operations Remote Fully Onsite

Customers globally rely on our extensive range of products and services—
from
life-saving medicines to lab essentials to next-generation instruments. Our Operations team leverages our PPI (Practical Process Improvement Business System) to manufacture and produce these products and continuously improve productivity and quality all while contributing to our Mission - to enable our customers to make the world healthier, cleaner and safer.
JOB DESCRIPTION

Work Schedule

Standard Office Hours (40/wk)

Environmental 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, Loud Noises (Equipment/Machinery), Office, Rapid flashing lights, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Standing for full shift

Job Description

Job Description

As an Engineer III, Manufacturing at Thermo Fisher Scientific, you will find yourself in an ambitious role within a company that champions innovation and excellence. This opportunity allows you to lead projects with a global impact while collaborating with a diverse and exceptionally talented team. You will play a crucial role in implementing flawless engineering solutions that contribute to our mission of making the world healthier, cleaner, and safer.

Job Responsibilities

  • Act as a leader and individual contributor on engineering projects
  • Mentor less experienced staff, nurturing relationships for project success
  • Lead initiatives centered around safety, quality, and delivery
  • Measure, track, and report project progress, driving projects to flawless completion
  • Remove obstacles and advance issues as needed to ensure business success
  • Foster a collaborative culture that brings out the best in team members and the cross functional team
  • Follow all plant safety and current Good Manufacturing Practices (cGMP) requirements
  • Develop User Requirement Specifications (URS)
  • Complete Field Acceptance Testing (FAT) and Site Acceptance Testing (SAT) using URS or equivalent experience
  • Support validation engineering activities including IQ, OQ, PV, and PQ
  • Build, complete, and document equipment and processes within the plant
  • Responsible for tooling, jig, and fixture design, documentation, validation and implementation
  • Apply statistical methods such as DOE, T-tests, ANOVA, Gage R&R to optimize manufacturing systems

Work Conditions

  • Varying amounts of time needed in the clean room operations depending on project phase
  • Occasionally required to stand, walk; frequently sit, use hands, talk, hear, and see
  • Occasionally lift/move up to 25 pounds; reasonable accommodations available
  • Occasionally exposed to mechanical parts, heights, fumes, airborne particles
  • Moderate to high noise levels; PPE required in production areas

Required Qualifications:

  • Bachelor's Degree in Engineering.
  • At least 5 years of engineering experience, preferably in GMP environment (Pharma / Biopharma)
  • Plastic injection molding experience is a strong bonus

Benefits

We offer competitive remuneration, annual bonuses, healthcare, and a range of employee benefits. Thermo Fisher Scientific provides a dynamic work environment with outstanding career development prospects. Our culture emphasizes integrity, intensity, involvement, and innovation.

Apply today! http://jobs.thermofisher.com

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