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Quality Control Chemist

Garonit Pharmaceutical
Posted 7 days ago, valid for 13 days
Location

Fairfield, NJ 07004, US

Salary

$55,000 - $66,000 per year

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Contract type

Full Time

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Sonic Summary

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  • Garonit Pharma is hiring a Quality Control Chemist for their onsite laboratory in Fairfield, NJ.
  • The role involves performing analytical testing and ensuring compliance with cGMP standards in pharmaceutical manufacturing.
  • Candidates should have a Bachelor’s degree in Chemistry or a related field and at least 1 year of experience in a Quality Control laboratory.
  • Key responsibilities include conducting USP testing, operating HPLC, and maintaining laboratory documentation.
  • The position requires strong attention to detail and familiarity with regulatory guidelines, but the salary information is not specified.

Quality Control Chemist

Onsite in Fairfield, NJ

Garonit Pharma is seeking a Quality Control Chemist to join our growing Quality team. This role will support analytical testing and laboratory operations for pharmaceutical manufacturing while ensuring compliance with cGMP standards and regulatory requirements.

Key Responsibilities

  • Perform sampling and analytical testing of raw materials, in-process materials, finished products, and packaging components
    • Conduct USP compendial testing and internal analytical methods
    • Operate laboratory instrumentation including HPLC and other analytical equipment
    • Support laboratory investigations, deviations, OOS results, and CAPA activities
    • Assist with analytical method development and validation
    • Perform environmental monitoring for air, water, and surfaces when required
    • Maintain laboratory documentation, logs, and batch record reviews in accordance with cGMP standards
    • Support regulatory and customer audits and assist with audit responses

Qualifications

  • Bachelor’s degree in Chemistry, Life Sciences, or a related scientific discipline
    • 1+ year of experience in a Quality Control laboratory preferred
    • Experience with pharmaceutical analytical testing and cGMP environments preferred
    • Familiarity with USP methods, laboratory documentation, and regulatory guidelines
    • Strong attention to detail and ability to work collaboratively in a regulated environment

About the Role

This position is fully onsite in our QC laboratory in Fairfield, NJ and involves routine use of analytical instrumentation and laboratory equipment.




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