Job Description
Step into a full-time QC Analyst I role at Bimeda, working the afternoon shift in Cambridge, ON. Engage with a variety of analytical techniques to ensure product quality.
As a QC Analyst I, you will report to the QC Supervisor and play a vital role in analyzing raw materials, in-process, and finished products. Your responsibilities will include conducting tests, preparing samples for analysis, and ensuring compliance with cGMP, SOPs, and Bimeda's quality standards. Collaborate with your team in a hands-on lab environment to achieve high-quality outcomes.
Key Responsibilities: • Conduct tests on raw materials and finished products • Perform identity testing on samples per schedule • Ensure compliance with GMP, GLP, and safety policies • Analyze data and report discrepancies to supervisor • Maintain clean work areas and calibrate equipment
Requirements: • 1-2 years in a pharmaceutical analytical lab • Bachelor’s degree in science, chemistry, or related field • ...
As a QC Analyst I, you will report to the QC Supervisor and play a vital role in analyzing raw materials, in-process, and finished products. Your responsibilities will include conducting tests, preparing samples for analysis, and ensuring compliance with cGMP, SOPs, and Bimeda's quality standards. Collaborate with your team in a hands-on lab environment to achieve high-quality outcomes.
Key Responsibilities: • Conduct tests on raw materials and finished products • Perform identity testing on samples per schedule • Ensure compliance with GMP, GLP, and safety policies • Analyze data and report discrepancies to supervisor • Maintain clean work areas and calibrate equipment
Requirements: • 1-2 years in a pharmaceutical analytical lab • Bachelor’s degree in science, chemistry, or related field • ...