Specialist 1, Quality Control

Becton Dickinson Medical DevicesEl Paso, TX
Onsite

About The Position

We are the people who give possibilities purpose. BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Requirements

  • Has an academic background and hands on laboratory training in the field of Chemistry.
  • Understands and consistently follows multi-step documented procedures.
  • Has hands on experience with USP/ISO/ASTM based chemical testing and performs all testing with strict adherence to the written laboratory work instructions.
  • Understands the validation principles for chemical methods, develops and validates new chemical test methods, and prepares study reports as required.
  • Bachelor's Degree in Chemistry
  • Familiar with GLP/GCP/cGMP practices.
  • Excellent communication and interpersonal skills.
  • Organized and self-motivated.

Nice To Haves

  • 2 years in analytical chemistry (preferred).
  • Experience in operating GC and HPLC (preferred).
  • Knowledge of FDA regulations for drugs and device desirable.

Responsibilities

  • Maintain Quality Reports.
  • Perform chemical analysis on drug products to include finish goods and/or stability product.
  • Maintain and implement efforts in housekeeping, and safety programs.
  • Must have awareness and respect of all company policies and safety rules.
  • Maintenance of the Calibration program for laboratory equipment.
  • Maintains accurate and well-organized laboratory records, notebooks and/or worksheets.
  • Use theoretical knowledge to interpret data and to trouble-shoot experiments.
  • Maintain assigned aspects of the chemistry laboratory work to provide material and technical support.
  • With moderate or no supervision, apply comprehensive understanding of defined productivity goals and objectives.
  • Maintain appropriate training/certification including GLP and GMP.
  • Perform other assigned tasks on as needed basis.
  • Must have awareness and respect of all company policies and safety rules.
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