• Los Angeles, CA
  • $30–$34 Per Hour
  • Contractor
  • Quick Apply
5 days ago

Job Description

Job Title:          Chemist I

Client:              Medical Device Manufacturing
Duration:         9 Months – Contract
Location:         Northridge, CA 91325
Shift:                1st Shift

 


Description:

Job Overview

Seeking an entry-level Chemist I to support a new product development project involving fillable cartridges. The role focuses on analytical testing, method development, laboratory instrumentation, data interpretation, and technical documentation within a regulated medical-device environment.

Job Responsibilities

Key Responsibilities

  • Perform qualitative and quantitative analysis of: Raw materials, In-process samples, Finished products
  • Perform analytical testing using: FTIR, ICP-MS, LC-UV, LC-MS
  • Support new product development and compatibility studies.
  • Assist with analytical method development and troubleshooting.
  • Interpret analytical data and identify potential issues.
  • Conduct exploratory research supporting product discovery and development.
  • Prepare and review test protocols, technical reports, and analytical data sheets.
  • Operate, maintain, and support laboratory instrumentation.
  • Accurately document testing activities, results, and deviations.
  • Follow cGMP, regulatory, laboratory safety, and quality requirements.
  • Provide general laboratory and project support.

Numbers & Facts

LocationLos Angeles, CA
Job TypeContractor
Salary$30–$34 Per Hour

Qualifications

Required Qualifications

  • Bachelor's degree in Chemistry or a related field.
  • 0+ years of relevant experience — suitable for entry-level candidates.
  • Hands-on experience with: FTIR, ICP-MS, LC-UV / LC-MS
  • Strong understanding of analytical chemistry techniques.
  • Strong data interpretation and troubleshooting skills.
  • Excellent documentation and attention to detail.
  • Proficiency with Microsoft Office Suite.
  • Ability to work independently and follow laboratory procedures and safety protocols. 

 

Preferred / Nice to Have

  • Knowledge of cGMP requirements.
  • Understanding of regulatory requirements for drug and medical-device testing.
  • Experience with analytical method development.
  • Experience working in a regulated laboratory environment. 

 

About Company

Medical Device Manufacturing

Skills

  • chemist

Skills

  • Analytical Method Developmentunmatched
  • Chemistryunmatched
  • Instrumentationunmatched
  • Manufacturingunmatched
  • Medical Equipmentunmatched
  • Product Developmentunmatched
  • Product Supportunmatched
  • Quality Assurance Methodologyunmatched
  • Technical Writingunmatched
  • Test Plan/Scheduleunmatched

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