Associate Scientist

EPM Scientific

Chicago (IL)

On-site

USD 75,000 - 85,000

Full time

14 days+

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Benefits offered by this job

Collaborative environment
Exposure to cutting-edge projects
Competitive compensation
Professional growth opportunities

Job summary

A leading pharmaceutical recruitment firm is seeking an entry-level Associate Scientist to join their team in Chicago. This role involves supporting analytical method development and routine testing with a focus on HPLC techniques. Candidates should have experience with oral solid dosage forms and a relevant degree in Chemistry or Pharmaceutical Sciences. A competitive compensation package and professional growth opportunities are offered.

Qualifications

  • Hands-on experience with HPLC in a pharmaceutical or academic setting.
  • Prior experience working with oral solid dosage forms in a development or QC environment.

Responsibilities

  • Perform routine and non-routine analysis of pharmaceutical samples using HPLC.
  • Support method development and validation for drug substances and products.
  • Conduct stability studies, dissolution testing, and content uniformity assessments.
  • Maintain accurate laboratory records in accordance with cGMP.
  • Interpret and report analytical data and troubleshoot instrumentation issues.

Skills

High-Performance Liquid Chromatography (HPLC)
Analytical techniques

Education

Bachelor's or Master's degree in Chemistry or Pharmaceutical Sciences

Tools

Empower
LIMS

Job description

This range is provided by EPM Scientific. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range: $75,000.00/yr - $85,000.00/yr

Direct message the job poster from EPM Scientific.

Overview

We are seeking a highly motivated and detail-oriented Associate Scientist to join our dynamic pharmaceutical development team. This role is ideal for individuals passionate about analytical chemistry and drug product development, particularly in the realm of oral solid dosage forms. The successful candidate will play a key role in supporting analytical method development, validation, and routine testing activities, with a strong emphasis on HPLC techniques.

Responsibilities
  • Perform routine and non-routine analysis of pharmaceutical samples using HPLC and other analytical techniques.
  • Support method development and validation for drug substances and drug products, with a focus on oral solid dosage forms (e.g., tablets, capsules).
  • Conduct stability studies, dissolution testing, and content uniformity assessments.
  • Maintain accurate and complete laboratory records in accordance with cGMP and regulatory requirements.
  • Interpret and report analytical data, troubleshoot instrumentation issues, and ensure timely delivery of results.
  • Collaborate cross-functionally with formulation scientists, quality assurance, and regulatory teams to support product development and lifecycle management.
  • Assist in the preparation of technical reports, protocols, and regulatory submission documents.
  • Ensure compliance with all safety and environmental regulations within the laboratory setting.
Qualifications

Required:

  • Hands-on experience with High-Performance Liquid Chromatography (HPLC) in a pharmaceutical or academic setting.
  • Prior experience working with oral solid dosage forms (e.g., tablets, capsules) in a development or QC environment.

Preferred (but not required):

  • Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
  • Familiarity with other analytical techniques such as UV-Vis, GC, FTIR, or dissolution testing.
  • Understanding of cGMP, ICH guidelines, and regulatory expectations for pharmaceutical development.
  • Experience with laboratory software systems (e.g., Empower, LIMS).
What We Offer
  • Opportunity to work in a collaborative and innovative environment.
  • Exposure to cutting-edge pharmaceutical development projects.
  • Competitive compensation and benefits package.
  • Professional growth and development opportunities.
Additional Information

This position is open to candidates who are currently authorized to work in the United States. Unfortunately, we are unable to offer visa sponsorship at this time.

Position Details
  • Seniority level: Entry level
  • Employment type: Full-time
  • Job function: Science
  • Industries: Chemical Raw Materials Manufacturing
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