Analytical Scientist - Early Career in OTC R&D

Haleon plc.

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
Paid parental leave
Healthcare coverage

Job summary

Haleon plc in Richmond, VA is seeking an Analytical Associate Scientist. You will support development of new OTC drugs by performing chemical and physical testing, applying established procedures, and contributing to method validation transfers.

The role emphasizes GMP, documentation, and collaboration with senior staff. Onsite with a 3-day in-office requirement, salary range provided in posting.

Qualifications

  • BS in Chemistry or related course of study.
  • Understanding GMP requirements and site policies & procedures.
  • 0+ years of relevant experience working in an analytical lab setting.
  • Industry laboratory experience preferred.

Responsibilities

  • Possesses basic knowledge of chemistry and laboratory techniques.
  • Applies technical skills and functional knowledge to projects and assignments.
  • Understands GMP requirements and R&D policies and procedures.
  • Completes all required training before conducting GMP scientific work.
  • Executes analytical procedures, methodologies, and method validation/transfer protocols under supervision.
  • Conducts analytical testing to support development of OTC drugs and medical devices.
  • Adheres to R&D documentation policies when recording scientific work.
  • Troubleshoots basic instrumentation issues.
  • Performs peer reviews of scientific data and reports.

Skills

Basic chemistry knowledge
GMP understanding
Analytical testing
Analytical methodology familiarity

Education

BS in Chemistry or related

Tools

HPLC
GC
Dissolution

Job description

Haleon plc in Richmond, VA is seeking an Analytical Associate Scientist. You will support development of new OTC drugs by performing chemical and physical testing, applying established procedures, and contributing to method validation transfers.

The role emphasizes GMP, documentation, and collaboration with senior staff. Onsite with a 3-day in-office requirement, salary range provided in posting.

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