Quality Control Analyst I Position Available In [Unknown county], Florida
Tallo's Job Summary: The Quality Control Analyst I position in Florida involves conducting Wet Chemistry testing, maintaining analytical instruments, and preparing solutions. The role requires experience with Labware LIMS V7, microbiology testing, and proficiency in MS Office. Candidates must have a Bachelor's degree in Chemistry or Microbiology and at least two years of experience in CGMP pharmaceutical or environmental laboratories.
Job Description
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Contact Us 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
