Quality Control Chemist at Cambrex in Charles City, Iowa

Posted in Other 9 days ago.





Job Description:


Cambrex


Quality Control Chemist

US-IA-Charles City

Job ID: 2024-3684
Type: Regular Full-Time
# of Openings: 1
Category: Quality Control
Cambrex - Charles City

Overview

Reporting to the QC Supervisor, the QC Chemist I is responsible for raw material, in-process, isolated intermediate, or finished good testing in a GMP laboratory environment.



Responsibilities

  • Adhere to all EPA, FDA, cGMP, cGLP DEA regulations and internal SOP's as they relate to the operation of the Quality Control lab and general operation of the chemical production facility
  • Follow all OSHA and company safety rules and practices
  • Data review
  • Data entry
  • Perform a wide variety of chemical analyses for release of raw materials, in-process, intermediates, finished goods, and stability
  • Maintain/support laboratory programs such as calibration/preventive maintenance, IQ/OQ/PQ
  • Perform in-depth laboratory investigations of non-complying test results.
  • Working knowledge of chromatography
  • Working knowledge of wet chemistry
  • Write controlled documents such as reports, test procedures, SOPs, etc.
  • Evaluate validity of test results
  • Independently troubleshoot equipment
  • Perform and document method transfer from Analytical Development
  • Run method evaluation experiments
  • Handle, analyze and dispose of hazardous samples and waste
  • Provide off-shift coverage as required
  • Maintain laboratory solutions, inventory and notebooks
  • Responsible for assisting in training employees as needed both inside and outside the department
  • Coordinate and communicate project status
  • Interacting with outside vendors and other departments
  • Extensive knowledge and proven ability to use a wide assortment of the analytical instrumentation available at Cambrex Charles City.
  • Proven ability to handle various assignments and organize workload to meet timelines

All employees are required to adhere to DEA, EPA, FDA and cGMP regulations as they relate to the operation of the Company; and to adhere to all company safety rules and procedures. All employees are expected to report to work regularly and promptly. Other duties relating to departmental mission, not specifically detailed in this section may be assigned.



Qualifications

  • BS/BA in Chemistry/Biology or related science field required
  • 2+ years laboratory cGMP environment with a BS or advanced degree






PI240043302

Salary:

$23.00


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