Amaris Consulting
Pharmaceutical – Quality Control Specialist
You will be supporting different projects through your expertise as a Quality Control Specialist.
Your Main Responsibilities
- Investigate nonconformities and determine corrective and preventive actions (CAPA).
- Perform cGMP-compliant testing as required to support Raw Material testing, In-process, Finished Product Release & Stability.
- Perform routine QC analysis (e.g. ELISA, UPLC/HPLC, CGE, GC, Particulates).
- Contribute to SOPs, protocols, technical studies, and reports.
- Perform preventative maintenance/calibration on basic laboratory equipment in accordance with established procedures.
- Support the development of Quality Systems in collaboration with on-site and global quality teams.
Qualifications
- Bachelor’s degree or diploma in chemistry, biology or a related field of study.
- 4+ years of related experience in a pharmaceutical cGMP environment.
- Knowledge of pharmaceutical GLPs and GMPs.
- Understanding of MS Office, LIMS, and SAP would be an asset.
- Knowledge of FDA, Health Canada regulations, and ICH guidelines.
- Demonstrated ability to work effectively in a team.
- Excellent communication skills in English.
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