Quality Control Analyst I

SGS_JOB_1352

Business Support
 Florida
Wet Chemistry testing
LOD
PH
API

Contract - 03-04+ Extendable Contract

This position performs testing of raw materials and drug products, maintenance and calibration of analytical instruments, prepares standard and sample solutions and maintains appropriate records.

Job Responsibilities:

  • Experience in Labware LIMS V7 and laboratory auditing processes
  • Microbiology testing experience on Environmental Samples for surface and air, Purified Water Samples, and RM/FP Microbial Limit Test following USP
  • Computer proficiency with comprehensive working knowledge of MS Office products, Learning Management Systems (LMS)
  • Ability to communicate effectively with excellent written and oral communication skills for scientific and/or technical ideas
  • Act independently and proactively to recommend methods and procedures for problem resolution
  • Self-directed with ability to organize and prioritize work
  • Understand Data Integrity (ALCOA+) and laboratory documentation practices

Skills:

  • Comply with all safety rules and regulations.
  • Perform analysis on raw materials, finish goods, API, and control substances
  • Ensures that balances are reviewed and calibrated.
  • Perform peer review of laboratory testing as required.
  • Responsible for Wet Chemistry testing (such as LOD, PH, titration, etc.)
  • Work within a team to meet productions, validation, stability, and request deadlines.
  • Participates in troubleshooting of analytical test methods and laboratory instruments.
  • Responsible for completing all training requirements and maintaining 100% compliance with all assignments.
  • Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), and Standard Operating Procedures (SOP’s) instructions.

Education/Experience:

  • Bachelor’s degree, preferably in Chemistry or Microbiology, or equivalent education/experience
  • Minimum of two years’ experience in Quality Control in CGMP pharmaceutical, biotechnology or environmental laboratory

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