Quality Control Analyst I Position Available In Broward, Florida
Tallo's Job Summary: The job of a Quality Control Analyst I in Sunrise, Florida, offers a salary range of $30 to $33 per hour in the pharmaceutical industry. The role requires a Bachelor's degree, 2+ years of experience in quality control, and proficiency in Labware LIMS V7. Responsibilities include testing raw materials, maintaining instruments, and ensuring compliance with laws and regulations. For further details, contact Himanshu Kumar Singh at himanshu.ksingh@collabera.com.
Job Description
Job Description
Quality Control Analyst I Contract:
Sunrise, Florida, US Salary Range:
30.00 – 33.00 |
Per Hour Job Code:
361213
End Date:
2025-05-22
Days Left:
27 days, 6 hours left To discuss more about this job opportunity, please reach out to Himanshu Kumar Singh(LinkedIn URL – https://www.linkedin.com/in/himanshu-kumar-singh-57b782258/), email your updated resume at Email – himanshu.ksingh@collabera.com or give me a call at (425) 403-0902. Thank you!
Pay Range:
$30 – $33/hour
Position Details:
Industry:
Pharmaceutical
Job Title:
Quality Control Analyst I
Duration:
6 months, with a possible extension
Location:
Sunrise, FL 33325 Requirements/ Nice to
Have:
Bachelor’s degree, preferably in Chemistry or Microbiology, or equivalent education/experience
Minimum of two years experience in a Quality Control in CGMP pharmaceutical, biotechnology or environmental laboratory
Experience to 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
Acts independently and proactively to recommend methods and procedures for problem resolution
Self-directed with ability to organize and prioritize workUnderstand Data Integrity (ALCOA+) and laboratory documentation practices
Position Summary:
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.
All areas of responsibility listed below are essential to the satisfactory performance of this position by any incumbents with reasonable accommodation if necessary. Any non-essential functions are assumed to be included in other related duties or assignments.
Carries out responsibilities in accordance with the organization’s policies, procedures, and state, Federal and
local laws.
Complies 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.
Responsible for performing additional related duties as assigned.
Job Requirement
GMP
cGMP
LIMS
Reach Out to a Recruiter
Recruiter
Email
Phone
Himanshu Singh
himanshu.ksingh@collabera.com