QC Lab technician
Apollo Health & Beauty Care Voir toutes les offres
- Toronto, ON
- 45.000 $ par an
- Permanent
- Temps-plein
- Gym Access
- Dental insurance
- Health insurance
- Performs physical and chemical testing on raw material, in-process, finished product, stability, and water samples.
- Responsible for the release of in-process samples and raw material samples upon completion of training and passing the qualification requirements.
- Maintains all related records within cGMP & GLP guidelines and provides accurate documentation of tests performed and results obtained.
- Ensure that all analytical test results are within the acceptable range specified on the Certificate of Analysis (CoA) forms.
- Ensures samples are submitted to the microbiological laboratory or dispatched to an external laboratory as required, in a timely manner.
- Performs laboratory equipment calibration in accordance with procedures, records results, and maintains calibration documentation.
- Investigates and documents out of specification (OOS) results.
- Files raw materials and external laboratory Certificates of Analysis (CoAs) into their respective binders.
- Provides experienced input regarding the development and amendment of procedures and practices in the analytical area.
- Recommend solutions for process improvements in the lab.
- Follows all Standard Operating Procedures (SOPs), health & safety procedures, and other applicable company policies.
- Wears, uses, and maintains personal protective equipment (PPE) as required.
- Uses equipment, materials, and machinery only as authorized.
- Identifies and reports any hazards, accidents, injuries requiring first aid, health care, lost-time injuries, occupational diseases, spills, or incidents in the workplace.
- Maintains laboratory equipment.
- Flexible shifts work as per business needs.
- Available to work extended hours and/or weekends as required.
- Performs other duties as assigned.
- Post-secondary degree in a related field.
- Prior experience working in environments governed by GMP and GLP standards. (1-3 years)
- Familiarity with regulatory requirements from US FDA, Health Canada, and ICH Guidelines.
- Excellent computer skills, along with strong written and oral communication abilities.
- High attention to detail and quality in documentation practices.
- Demonstrated proficiency in General Chemistry and use of analytical instruments, including HPLC, GC, ICP, UV-VIS, FTIR, and Titrations.
- Strong ability to multi-task and effectively prioritize work.
- Capable of performing routine and new procedures with minimal supervision.
- Proven ability to interact across all organizational levels to support goals and influence decisions.
- Solid understanding of statistics with the ability to analyze and present data in a clear, visual format.