QC Chemist II — HPLC/GC Specialist in GMP Environments

Actalent

Columbus (OH)

On-site

USD 39,000 - 41,000

Full time

8 days ago

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Job summary

Actalent is seeking a Chemist in Columbus, OH for a contract-to-hire role focused on analytical testing of APIs and materials. You will perform qualitative and quantitative analyses using HPLC/GC, validate methods, and prepare technical reports in a GMP/FDA-regulated setting.

The candidate should hold a BSc/MSc in Chemistry or Biochemistry with 3+ years of relevant industry experience, strong communication skills, and the ability to manage multiple tasks in a fast-paced team environment.

Qualifications

  • Bachelor's or Master's degree in a scientific field, preferably Chemistry or Biochemistry.
  • 3+ years of industry Chemistry experience with heavy HPLC or GC.
  • Strong knowledge of HPLC, GC, and GMP/FDA-regulated environments.
  • Ability to work in a fast-paced, multi-project setting.
  • Excellent written and verbal communication skills.
  • Experience in quality is a plus.
  • Team-oriented with ability to work under supervision.

Responsibilities

  • Perform qualitative, quantitative chemical and physical testing for APIs, starting materials, packaging components, and finished products.
  • Conduct peer reviews of analytical testing documentation.
  • Maintain laboratory data in notebooks, worksheets, and documents.
  • Re-validate methods and work with HPLC, GC, Wet Chemistry.
  • Author technical reports for analytical methods improvement.
  • Troubleshoot analytical procedures and instruments.
  • Communicate effectively in writing and verbally.

Skills

HPLC experience
GC experience
Quality experience
Team collaboration
Communication skills
Laboratory testing
GMP/FDA experience
Scientific judgment

Education

Chemistry/Biochemistry degree

Tools

HPLC instrumentation
GC instrumentation

Job description

Actalent is seeking a Chemist in Columbus, OH for a contract-to-hire role focused on analytical testing of APIs and materials. You will perform qualitative and quantitative analyses using HPLC/GC, validate methods, and prepare technical reports in a GMP/FDA-regulated setting.

The candidate should hold a BSc/MSc in Chemistry or Biochemistry with 3+ years of relevant industry experience, strong communication skills, and the ability to manage multiple tasks in a fast-paced team environment.

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