QC EngineerScientist I

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profile Job Location:

Madison, OH - USA

profile Monthly Salary: Not Disclosed
Posted on: 9 hours ago
Vacancies: 1 Vacancy

Job Summary

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 Laboratory Setting Office Warehouse

Job Description

As part of the Thermo Fisher Scientific team youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

LOCATION: This is a fully onsite position based at our Madison WI site. Unfortunately relocation assistance is NOT provided.

  • Must be legally authorized to work in the United States without sponsorship now or in the future.
  • Must be able to pass a comprehensive background check which includes a drug screen.

DESCRIPTION:
Be part of our Quality Control team at Thermo Fisher Scientific where youll contribute by ensuring the quality and reliability of products that help make the world healthier cleaner and safer. Youll perform testing and analysis to support the development of innovative therapeutic products. Youll conduct quality control testing of raw materials in-process samples and finished products using various analytical techniques. Youll document and analyze test results participate in investigations and contribute to continuous improvement initiatives. This role offers opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.

REQUIREMENTS:

  • Bachelors degree in engineering prior experience preferred in quality control in a laboratory environment manufacturing/biotech industry
  • Strong knowledge in IS0 requirements and quality management systems (QMS)
  • Strong analytical and problem-solving skills with emphasis in root cause analysis (RCA)
  • Lead or support deviation investigations CAPAs and change controls
  • Ability to follow SOPs Validation records Test Reports batch records and ensuring traceability and compliance
  • Support audit readiness (internal regulatory customer)
  • Strong computer skills in Microsoft Office and analytical software
  • Excellent attention to detail and organizational skills
  • Ability to work both independently and collaboratively in a cross functional team environment
  • Clear written and verbal communication skills
  • Experience with laboratory equipment maintenance and calibration
  • Knowledge of relevant regulatory requirements
  • Ability to manage multiple priorities effectively
  • Flexible scheduling may be required


Required Experience:

IC

Work ScheduleStandard Office Hours (40/wk)Environmental ConditionsAble to lift 40 lbs. without assistance Adherence to all Good Manufacturing Practices (GMP) Safety Standards Laboratory Setting Office WarehouseJob DescriptionAs part of the Thermo Fisher Scientific team youll discover meaningful work...
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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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