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QC Analyst

Job in Cleveland, Cuyahoga County, Ohio, 44101, USA
Listing for: Trident Consulting
Full Time position
Listed on 2025-12-27
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below

Position: QC Analyst (2nd Shift)

Location:

4353 East 49th Street, Cleveland, OH 44125, USA

Shift: 2nd Shift | Monday–Friday, 2:00 PM — 10:30 PM

Work Hours:

40 hours/week (8 hours/day)
Bill rate: $39.75 – $59.75

Overview

Due to increased business needs, we are seeking a highly skilled QC Analyst to support Quality Control operations on the 2nd shift. This role requires strong analytical testing experience, method validation expertise, and the ability to independently handle GMP laboratory processes.

Essential Job Functions & Responsibilities

Analytical Testing & Instrumentation

  • Perform analytical testing using:
    • IR
    • pH
    • TLC plates
    • Solubility
    • Other wet chemistry methods
  • Perform analytical testing using HPLC instrumentation.
  • Follow Compendial testing methods (USP/EP/JP) accurately.
  • Utilize written procedures to perform all testing activities.

Documentation & Review

  • Complete peer reviews of analytical data.
  • Draft and execute validation protocols.
  • Write reports for completed validation protocols.
  • Serve as technical reviewer for protocols and reports.
  • Apply Good Documentation Practices (GDP) and Data Integrity principles.

Investigations & Quality

  • Identify Out-of-Specification (OOS) results.
  • Lead or support investigations with minimal guidance.
  • Determine root cause and recommend corrective actions when applicable.
  • Perform scheduled verification/calibration of instruments or titrants.

Operational Excellence

  • Plan and organize tasks effectively with minimal oversight.
  • Manage larger projects/processes independently.
  • Maintain a clean, safe, and compliant laboratory environment.
  • Follow all cGMP, ISO
    9001/14001/45001, and safety procedures.
  • Participate in process improvement, safety initiatives, and 5S activities.

Teamwork & Conduct

  • Demonstrate professional behavior with colleagues and visitors.
  • Work effectively in a team environment.
  • Uphold company Core Values:
    Courage, Respect, Achievement, Integrity, Responsibility, Transparency.
Education & Experience Requirements
  • Option 1: Bachelor’s degree in Chemistry or Life Science;
    Minimum 5 years laboratory experience.
  • Option 2: Associate degree in Chemistry or Life Science;
    Minimum 10 years laboratory experience (non-academic labs).

Additional Required Expertise:

  • Method Validation
  • Compendial Testing (USP/EP/JP)
  • Experience working in GMP laboratory environments
Additional Requirements
  • Employment Testing:
    • Pre-/Annual-employment medical screening
    • Background check
    • Drug/alcohol screening
  • Physical Requirements:
    • Ability to stand for extended periods
    • Ability to lift up to 25 lbs
    • Exposure to chemicals requiring PPE
  • Requirements For:
    • Forklift operation
    • Respirator use
    • Laser operation
    • Animal handling
Vaccinated Pathogen Work

Assignment Details:

  • Contingent Type:
    Classic
  • Order Reason:
    Spike in business needs
  • Timesheet:
    Time in/Time out (Weekly)
  • Hours for Estimated Spend: 2,080
  • Estimated Additional Spend: 10%
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