Job Description

Job Summary

We are seeking a meticulous and detail-oriented Quality Control Analyst to join our team. The Quality Analyst will play a crucial role in ensuring that our products meet the highest standards of quality and compliance.

Under the supervision of the QC Supervisor, the Quality Control Analyst's main role is to support manufacturing process for timely and effective GMP review of production records, and to inspect and control materials used for the product realization including non-conforming products. This position reports to the Quality Control Supervisor.

Primary Responsibilities:

Conduct inspections, sampling, and identification of incoming shipment(s) of raw material, packaging material and bulk products including intermediate products for all stages in production, such as Dispensing and Blending, Encapsulation or Tableting, Bottling and Labelling. Quarantine, release, or reject incoming shipments, labels, intermediate, in-process and finished products as per written specifications. Prepare samples for raw materials, in-process and finished products, air and water and coordinate testing activities with 3rd party labs. Administrative tasks which involve data entry of lab results, scanning and filing of COAs and invoices check Provide Testing of raw material for moisture contents, particle size, density, flow-ability, and compressibility (using Hauser ratio and Carr index) and Identity test as per standard operating procedures Ensure good documentation practices are followed to ensure traceability. Data retrieval, entry, and analysis of processes. Investigate OOS testing deviations occur to determine possible and definite causes and ensure future prevention of such mishaps, and whether the impacted product is suitable for release. Prepare samples and coordinate testing activities with 3rd party labs Administrative tasks which involve data entry of lab results, scanning and filing of COAs and invoices check Work directly with Production to understand and report component quality issues. Work with Quality Assurance Team for their resolution Organizing and Filing of records Generating and reviewing processes (work instructions/ SOPs) pertaining to job functions Calibration and validation of in-process QC instruments Daily balance verification and Hygiene monitoring Generating and reviewing processes (work instructions/ SOPs) pertaining to job functions Assist in various projects as assigned Other QC duties may be assigned

Qualifications and Requirements

:

Degree or Diploma in Chemistry or Biological Science required with 3 or less years of experience in GMP manufacturing Pharma or Food operations Moderate to advanced Microsoft programs such Excel and Word Strong organization skills and resourceful Excellent communication and interpersonal skills Possess enthusiasm and effective training capabilities Work effectively independently and as a team member Effective organizational skills Proficient in English spoken and written Good command of computer applications Excel and Microsoft office
Join us as we strive for excellence in our products and services, ensuring that every item meets our high-quality standards!

Job Types: Full-time, Permanent

Benefits:

Casual dress Company events Dental care Disability insurance Employee assistance program Extended health care Flexible schedule Life insurance On-site parking Paid time off RRSP match Store discount Vision care Wellness program
Work Location: In person