QC Scientist I

at  Thermo Fisher Scientific

St. Louis, MO 63134, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate14 Feb, 2025Not Specified16 Nov, 20241 year(s) or abovePowerpoint,Iso,Excel,Flawless Execution,Cgmp Practices,Root Cause AnalysisNoNo
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Description:

JOB DESCRIPTION

At Thermo Fisher Scientific Inc., we are committed to making the world healthier, cleaner, and safer. As a QC Scientist I, you will play a vital role in our mission by ensuring the highest standards of environmental monitoring and quality control. This is an outstanding opportunity to join an ambitious team that values collaboration and innovation. Your work will have a real-world impact in areas such as cancer research, environmental protection, and food safety.

WHAT WE DO

  • Perform routine environmental monitoring of viable/non-viable air, contact surfaces, water, and gases in accordance with site procedures.
  • Document all activities to meet cGMP requirements and perform document reviews and revisions.
  • Interpret data results using concepts of microbiology, industry standards, and site SOPs and policies.
  • Evaluate processes critically, including foresight and proactive thinking.
  • Complete preventative maintenance and work notifications on time, perform equipment testing, and routine troubleshooting.
  • Prioritize tasks by interpreting production schedules and complete tasks accordingly.
  • Identify deviations, aid in investigations, and analyze root causes. Complete documentation of deviations and events in appropriate systems.
  • Participate in one-on-ones, department meetings, and other meetings to facilitate area needs based on changes.

How will you get here?

  • No experience required, but 1-3 years of relevant lab experience in a related field or industry preferred.
  • Bachelor’s degree
  • Experience in cGMP environment preferred.
  • Experience with using an autoclave, water testing, and environmental monitoring in ISO classified areas seen as a plus.

KNOWLEDGE, SKILLS, ABILITIES

Knowledge

  • Understanding of cGMP practices, aseptic techniques, or microbiological concepts is a plus.
  • Familiarity with industry standards such as ISO, ICH, FDA, and USP.

SKILLS

  • Proficiency in MS Office (Word, Excel, PowerPoint, etc.).
  • Strong prioritization skills.
  • Diligent with a focus on flawless execution.
  • Experience with Root Cause analysis preferred.

ABILITIES

  • Ability to read, write, and communicate effectively in English.
  • Ability to work in clean-room environment and execute aseptic practices.
  • Ability to lift 40 pounds and stand for over 4 hours.
  • Ability to understand and carry out instructions reliably.
  • Effective communication skills (written and verbal).
  • Ability to effectively multi-task and work in a dynamic environment.
  • Ability to work independently and as part of a collaborative team.
  • Awareness to identify problems before they occur and address them proactively.
    Join us and contribute to groundbreaking work that truly makes a difference. Apply your skills in a world-class environment where you are supported to achieve your career goals

Responsibilities:

Please refer the Job description for details


REQUIREMENT SUMMARY

Min:1.0Max:3.0 year(s)

Information Technology/IT

Pharma / Biotech / Healthcare / Medical / R&D

Software Engineering

Graduate

Proficient

1

St. Louis, MO 63134, USA