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Tunnell Consulting, Inc.


Quality Control Analyst

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Recruitment began on June 9, 2025
and the job listing Expires on December 9, 2025
Full-time, Internship, Part-time
Apply Now

Quality Control Analyst

Birmingham, AL

Tunnell Consulting is an employee-owned, life sciences management consulting firm. Known for solving complex problems in the life sciences, we support the mission and objectives of a variety organizations including biotech, pharma, the U.S. Government, foundations, public/private partnerships, investors, and emerging companies. The variety of clients and issues that we support give our team and our organization an ever-increasing breadth of experience to add to our deep industry and functional expertise. Headquartered in the Philadelphia area, we also have a presence in Washington DC, and Boston.

Job Title: QC Analyst – HPLC Specialist
Employment Type: 40 hour/week contract role

Job Summary:

Tunnell is seeking a detail-oriented and experienced Quality Control (QC) Analyst with hands-on expertise in performing assays using High-Performance Liquid Chromatography (HPLC). In this role, the QC Analyst will be responsible for conducting analytical testing of raw materials, in-process samples, and finished products in compliance with cGMP standards and regulatory requirements. This is estimated to be a 3-month project with potential for temp to perm conversion. Client is based in the greater Birmingham, AL area. Local candidates only.

Key Responsibilities:

  • Perform qualitative and quantitative testing using HPLC, following established SOPs and analytical methods.
  • Interpret chromatograms, troubleshoot HPLC instrumentation issues, and ensure accurate, reliable data reporting.
  • Prepare samples and standards in accordance with method requirements.
  • Document all work in accordance with Good Documentation Practices (GDP).
  • Support method development, validation, and transfer activities as needed.
  • Maintain laboratory equipment, ensuring regular calibration and qualification.
  • Contribute to laboratory investigations and contribute to CAPA (Corrective and Preventive Actions) when deviations occur.
  • Collaborate with cross-functional teams including R&D, QA, and production.
  • Follow all safety and compliance protocols within the laboratory environment.

Qualifications:

  • Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or related field.
  • 2-3 years of experience in a QC laboratory environment, with proven proficiency using HPLC (e.g., Waters, Agilent systems).
  • Familiarity with cGMP and regulatory guidelines (FDA, ICH).
  • Experience with additional analytical techniques such as UV-Vis, GC, FTIR, or Dissolution is a plus.
  • Strong technical writing and documentation skills.
  • Ability to work independently and as part of a team in a fast-paced environment.

Preferred Skills:

  • Experience with chromatography software (e.g., Empower, ChemStation).
  • Knowledge of pharmaceutical or biotech product testing.
Apply Now
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