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Engineer III, Manufacturing Process
Engineer III, Manufacturing ProcessThermo Fisher Scientific • Indianapolis, Indiana, USA
Engineer III, Manufacturing Process

Engineer III, Manufacturing Process

Thermo Fisher Scientific • Indianapolis, Indiana, USA
[job_card.variable_hours_ago]
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  • [job_card.full_time]
[job_card.job_description]

Work Schedule

First Shift (Days)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards Cleanroom : no hair products jewelry makeup nail polish perfume exposed piercings facial hair etc... allowed Office Some degree of PPE (Personal Protective Equipment) required (safety glasses gowning gloves lab coat ear plugs etc.)

Job Description

Location / Division Specific Information

Join Thermo Fisher Scientifics Clinical Trial Division and help support lifesaving clinical this role you will contribute to the packaging and preparation of clinical trial drug products that reach patients around the world. You will work on meaningful projects partner with supportive teams and help shape processes that improve quality and patient care.

As a Manufacturing Engineer you will develop equipment qualifications process documentation and packaging components such as labels inserts and cartons. You will also support manual semi-automated and automated packaging processes including auto-injector systems. This role offers hands-on work collaboration and opportunities to innovate.

We have 2 positions available.

What will you do

  • Provide technical support that helps maintain safe and consistent production.
  • Build manufacturing processes that increase quality reliability and sustainability.
  • Create and test automated solutions that simplify workflows and improve performance.
  • Support installation and integration of automation tools such as PLCs robotics and machine-vision systems.
  • Troubleshoot equipment review data and identify opportunities for improvement.
  • Partner with operations quality and engineering teams to strengthen processes.
  • Lead problem-solving activities including root-cause analysis and risk-reduction efforts.
  • Write clear documentation including SOPs protocols and study reports.
  • Participate in equipment testing FATs SATs and qualification activities.
  • Support continuous-improvement projects using Lean and Six Sigma practices.
  • Stay current on new technologies that can enhance our systems and workflow.

Education & Experience

  • Bachelors degree in Mechanical Electrical Industrial Automation or Manufacturing Engineering.
  • Minimum 3 years experience in GMP pharmaceutical biotech or regulated manufacturing environments.
  • Experience with automation systems or process automation in a production setting.
  • Familiarity with CAD tools such as SolidWorks or AutoCAD.
  • Experience with statistical analysis or DOE tools (JMP experience is a plus).
  • Knowledge of automation data integrity and audit trail systems is helpful.

    • Skills That Help You Succeed

  • Collaborative communication style and ability to work well with cross-functional teams.
  • Strong analytical and creative problem-solving skills.
  • Comfort working with data and making informed balanced recommendations.
  • Understanding of Lean or continuous-improvement concepts.
  • Ability to support several projects and tasks at once.
  • Attention to detail and an interest in learning new tools and technologies.

    • Preferred Qualifications

  • Experience in biotech or regulated packaging environments.
  • Familiarity with PLCs robotics or machine-vision systems.
  • Experience in automation assembly or integration.

    • Work Environment

  • Follows Good Manufacturing Practices (GMP) and site safety standards.
  • May involve cleanroom work with specific grooming and dress requirements.
  • Includes both office and production-floor responsibilities.
  • May require PPE such as safety glasses gloves ear protection or gowns.

    • Excellent Benefits

  • Benefits & Total Rewards Thermo Fisher Scientific
  • Medical Dental & Vision benefits-effective Day 1
  • Paid Time Off & Designated Paid Holidays
  • Retirement Savings Plan
  • Tuition Reimbursement

    • OTHER

  • Relocation assistance is NOT provided
  • Must be legally authorized to work in the United States without sponsorship.
  • Must be able to pass a comprehensive background check which includes drug screening

    • Key Skills

    Lean Manufacturing,Six Sigma,CNC Programming,Lean,Machining,Tooling,CAD,CNC,Assembly Experience,SolidWorks,Kaizen,Manufacturing

    Employment Type : Full-Time

    Experience : years

    Vacancy : 1

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