Quality Control PChem Analyst I or II

CLENE NANOMEDICINE INCNorth East, MD
$25 - $28Onsite

About The Position

We are seeking a detail-oriented and motivated Quality Control P-Chem Analyst I or II to join our Quality Control team. In this role, you will support the analysis of bioanalytical and production samples while helping ensure the quality, safety, and integrity of our products. If you enjoy working in a collaborative laboratory environment focused on scientific excellence and continuous improvement, we'd love to hear from you.

Requirements

  • Bachelor's degree in Chemistry, Biology, Biochemistry, Pharmaceutical Sciences, or another related scientific discipline preferred.
  • Equivalent combinations of education and relevant laboratory experience will be considered.
  • Quality Control Analyst I: One (1) year of laboratory experience.
  • Quality Control Analyst II: Two (2) to three (3) or more years of progressively responsible laboratory experience, preferably in a regulated pharmaceutical, biotechnology, or medical device environment.
  • Working knowledge of cGMP and cGLP requirements
  • Strong analytical and problem-solving skills
  • Experience operating analytical laboratory instrumentation
  • Excellent attention to detail and organizational skills
  • Strong written and verbal communication skills
  • Proficiency with Microsoft Office applications
  • Ability to work independently while collaborating effectively with a team
  • Ability to read, interpret, and follow technical documents, SOPs, and laboratory procedures
  • Commitment to safety, quality, accuracy, and continuous improvement

Responsibilities

  • Perform analytical testing of bioanalytical specimens, including blood, urine, and tissue samples.
  • Analyze production and research samples using laboratory instrumentation and analytical techniques.
  • Operate, maintain, calibrate, and troubleshoot laboratory equipment and analytical instruments.
  • Follow all Standard Operating Procedures (SOPs), Test Methods (TSMs), cGMP, cGLP, and internal quality processes.
  • Assist with laboratory equipment qualification, validation, and calibration activities.
  • Prepare, revise, and maintain test methods, SOPs, and other quality documentation.
  • Review analytical data for accuracy and completeness.
  • Identify and communicate issues that could affect product identity, strength, quality, purity, compliance, or laboratory efficiency.
  • Support Research & Development projects and laboratory investigations.
  • Maintain laboratory inventory, Safety Data Sheets (SDS), and assist with purchasing laboratory supplies.
  • Complete all required training and maintain training records.
  • Participate in continuous improvement initiatives.
  • Perform other duties as assigned.

Benefits

  • Up to 4 weeks of paid vacation
  • Paid holidays
  • Medical, dental, vision, and prescription insurance for employees and eligible dependents
  • 401(k) retirement plan with employer match
  • Opportunities for professional growth and continued learning
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