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Associate Scientist III – Quality Control

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Carex Consulting Group

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Location:
United States , Madison, Wisconsin

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Category:
Pharmacy

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Contract Type:
Not provided

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Salary:

Not provided
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Job Description:

Carex is partnering with Pharmaceuticals industry partner to hire an Associate Scientist III – Quality Control to support pharmaceutical testing within a cGMP-regulated environment. This role focuses on routine analytical testing of raw materials, in-process samples, drug substances, and stability samples, including those for GLP Toxicology and clinical trial release. The Associate Scientist III is expected to operate various analytical instruments, contribute to lab operations, and uphold rigorous documentation and compliance standards while working under laboratory leadership.

Job Responsibility:

  • Perform analytical testing of pharmaceutical raw materials, intermediates, finished products, and stability samples using established methods
  • Operate and maintain analytical instrumentation (e.g., HPLC, GC, FT-IR, UV/Vis, KF) with minimal supervision
  • Execute tasks in accordance with cGMP, GLP, and SOP requirements, contributing to project timelines and deliverables
  • Draft and contribute to technical documentation including investigations, deviations, and CAPAs
  • Identify and troubleshoot analytical, instrumentation, and data-related issues, escalating as needed
  • Maintain accurate records in lab notebooks and worksheets, ensuring compliance with documentation standards
  • Review data generated by peers, ensuring quality and integrity of results
  • Participate in instrument calibration, maintenance, and troubleshooting
  • Collaborate cross-functionally within the lab and demonstrate adaptability to shifting priorities
  • Train on laboratory procedures and contribute to a culture of continuous learning and compliance

Requirements:

  • Bachelor’s degree in Chemistry or a related scientific discipline
  • Minimum of 5 years of relevant laboratory experience in a cGMP-compliant setting
  • Proficiency in operating and troubleshooting analytical instrumentation
  • Working knowledge of cGMP requirements, laboratory operations, and associated software systems
  • Strong analytical thinking, written and verbal communication skills
  • Ability to interpret technical documents, perform complex calculations, and present findings effectively
  • Detail-oriented approach with a commitment to scientific accuracy and quality
  • Demonstrated initiative in learning new techniques and working independently as well as collaboratively

Additional Information:

Job Posted:
January 26, 2026

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