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Quality Control Specialist

Job in El Paso, El Paso County, Texas, 88568, USA
Listing for: Software Technology, Inc.
Full Time position
Listed on 2026-07-15
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control - QC Analysts/Managers
Salary/Wage Range or Industry Benchmark: 52000 - 78000 USD Yearly USD 52000.00 78000.00 YEAR
Job Description & How to Apply Below
Position: Quality Control Specialist 1

Overview

Job Title: Quality Control Specialist 1
Location: El Paso, TX
Duration: 12+ months
Shift hours: Mon‑Fri 8:00 am‑5:00 pm, overtime as needed
Interviews: In person

Must haves on the resumes:

  • Laboratory experience
  • General chemistry background
  • Organization and time management

Education:

  • Bachelor's Degree in Chemistry, Microbiology, or another related Life Science
Responsibilities
  • Maintain quality reports.
  • Perform chemical analysis on drug products, including finished goods and/or stability products.
  • Maintain and implement housekeeping and safety programs.
  • Ensure awareness and respect of all company policies and safety rules.
  • Maintain the calibration program for laboratory equipment.
Requirements
  • Academic background and hands‑on laboratory training in chemistry.
  • Understand and consistently follow multi‑step documented procedures.
  • Hands‑on experience with USP/ISO/ASTM based chemical testing; perform all testing with strict adherence to written laboratory work instructions.
  • Understand validation principles for chemical methods, develop and validate new chemical test methods, and prepare study reports.
  • Maintain accurate and well‑organized laboratory records, notebooks, and worksheets.
  • Use theoretical knowledge to interpret data and troubleshoot experiments.
  • Maintain assigned aspects of the chemistry laboratory work to provide material and technical support.
  • Apply comprehensive understanding of defined productivity goals and objectives with moderate or no supervision.
  • Maintain appropriate training and certification including GLP and GMP.
  • Knowledge of FDA regulations for drugs and devices is desirable.
  • Perform other assigned tasks as needed.
  • Ensure awareness and respect of all company policies and safety rules.
Qualifications
  • Bachelor's Degree in Chemistry, Microbiology, or another related Life Science.
  • Minimum 2 years in analytical chemistry (preferred).
  • Experience operating GC and HPLC (preferred).
  • Familiarity with GLP, GCP, and cGMP practices.
  • Excellent communication and interpersonal skills.
  • Organized and self‑motivated.
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