Research Analyst I: Formulations & Lab Compliance

Charles River Laboratories

Ashland (OH)

Vor Ort

USD 42.000 - 46.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Charles River Laboratories is seeking a Research Analyst I to prepare dosing materials and samples for various formulations, with oversight. The role emphasizes accurate documentation, GMP/GxP-like compliance, and safe handling in a lab setting.

You will sterilize equipment, assist with glassware maintenance, and contribute to process improvements while supporting study directors and teams in a fast-paced environment.

Qualifikationen

  • Bachelor's degree in laboratory science or related discipline required.
  • HS Diploma/GED with 2 years of lab experience acceptable.
  • Strong written and verbal communication skills essential.
  • Ability to manage multiple tasks and priorities to achieve goals.

Aufgaben

  • Prepare basic to complex dosing material and samples for solutions, suspensions, diets, and dispensations.
  • Efficiently document procedures, materials, and results in compliance with protocols and SOPs.
  • Independently sterilize laboratory equipment using autoclave or other methods.
  • Assist in washing and maintenance of glassware and lab cleanliness.
  • Assist with disposal of residual dosing material.
  • Demonstrate effective communication with peers, supervisor, and team.
  • Identify equipment issues for troubleshooting and notify appropriate personnel.
  • Participate in process improvement initiatives.
  • Provide feedback on laboratory investigations and quality observations.
  • Prepare aseptic formulations with oversight.

Kenntnisse

Communication skills
Multitasking
Computer literacy
Safety procedures

Ausbildung

Bachelor's degree in laboratory science or related discipline
HS Diploma / GED with 2 years lab experience

Jobbeschreibung

Charles River Laboratories is seeking a Research Analyst I to prepare dosing materials and samples for various formulations, with oversight. The role emphasizes accurate documentation, GMP/GxP-like compliance, and safe handling in a lab setting.

You will sterilize equipment, assist with glassware maintenance, and contribute to process improvements while supporting study directors and teams in a fast-paced environment.

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