Quality Control Inspector at Software Technology Inc
El Paso, Texas, USA -
Full Time


Start Date

Immediate

Expiry Date

05 Jun, 25

Salary

0.0

Posted On

03 May, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Analytical Chemistry, Chemical Testing, Microbiology, Life Science, Academic Background, Interpersonal Skills, Study Reports, Chemistry, Gmp

Industry

Pharmaceuticals

Description

3 must haves on the resumes: Laboratory experience, general chemistry background, organization, and time management.
Education - Bachelor’s Degree in Chemistry or Microbiology or other related Life Science
Specialist 1, Quality Control

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.
  • 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.
  • Knowledge of FDA regulations for drugs and device desirable.
  • Perform other assigned tasks on as needed basis.
  • Must have awareness and respect of all company policies and safety rules.

QUALIFICATIONS:

  • Bachelor’s Degree in Chemistry or Microbiology or other related Life Science.
  • 2 years in analytical chemistry (preferred).
  • Experience in operating GC and HPLC (preferred).
  • Familiar with GLP/GCP/cGMP practices.
  • Excellent communication and interpersonal skills.
  • Organized and self-motivated.
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.
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