Analytical Scientist I - GMP Lab, HPLC/GC

Haleon

Richmond (VA)

On-site

USD 66,000 - 91,000

Full time

9 days ago

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Benefits offered by this job

401(k) plan
Tuition reimbursement
6 months parental leave
Healthcare coverage
Discretionary bonus

Job summary

Haleon in Richmond, VA is seeking an Associate Analytical Scientist to join the Global R&D OTC team. The role focuses on analytical testing of products under development, applying GMP practices, and gaining proficiency with HPLC, GC, and dissolution techniques.

This onsite position requires a dedication to quality and accurate data recording. You will execute established procedures, perform method transfers, and support new OTC drug development under supervision, contributing to a robust

Qualifications

  • BS in Chemistry or related course of study.
  • 0+ years of relevant experience in analytical lab.
  • Working knowledge of GMP requirements and site policies & procedures.
  • Experience with HPLC, GC and dissolution.

Responsibilities

  • Executes analytical procedures, methodologies, and method validation/transfer protocols under senior supervision.
  • Conducts analytical testing (chemical and physical) to support the development of new OTC drugs and medical devices.
  • Adheres to R&D documentation policies when recording scientific work.
  • Identifies atypical data and collaborates with a senior colleague to investigate root causes.
  • Troubleshoots basic instrumentation issues.
  • Performs peer reviews of scientific data and reports, resolving issues promptly.

Skills

Chemistry basics
Analytical lab skills
GMP understanding
Troubleshooting

Education

BS in Chemistry

Tools

HPLC
GC
Dissolution testing

Job description

Haleon in Richmond, VA is seeking an Associate Analytical Scientist to join the Global R&D OTC team. The role focuses on analytical testing of products under development, applying GMP practices, and gaining proficiency with HPLC, GC, and dissolution techniques.

This onsite position requires a dedication to quality and accurate data recording. You will execute established procedures, perform method transfers, and support new OTC drug development under supervision, contributing to a robust

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