QC Chemist

Job description

Job Overview

The QC Chemist Chemist as part of the technical transfer group is responsible for conducting testing to support the introduction of new products

Job Responsibilities

  • The QC Chemist will be responsible for completing all testing in a timely manner that supports established production targets and SLAs.
  • Maintain data integrity and ensure compliance with FDA, GLP, QSR and cGMP regulations, as well as with company SOPs and specifications.
  • Observe established escalation process for laboratory issues that impact established production-related Service Level Agreements (SLAs) and/or the fulfilment of production goals.
  • The QC Chemist will participate in investigations and root cause analysis.
  • Author documents that ensure cGMP compliance, such as laboratory investigation, deviations, change controls, change notices, analytical test methods, method development/validation protocols and reports and method verification protocols and reports.
  • The QC Chemist will seek process innovation and continuous process improvement and perform quality improvement initiatives in the laboratory to meet site production goals.
  • Complete and conform to all training requirements for job role, including company-required and job role-specific training.

The next QC Chemist should have a minimum of a Bachelor’s Degree qualification in Chemistry or related Science with at least 2 years relevant laboratory experience in a cGMP environment.  You should have experience in method validation and or transfer for analytical methods including HPLC/UPLC or GC.

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