Technical Document Reviewer

ü  Improve, proof-read and update content of technical documents (SOPs, forms, analytical methods, etc.)

ü  Perform occasionally some Microbiology testing (USP 61, USP 62)

ü  Maintain master spreadsheets (chemicals and standards, documents, procedures, etc.)

ü  Participate in internal audit program (calibration related documents and QC documents)

ü  Assist the Quality Director whenever it is necessary

Raises any flags to Directors regarding any quality issue or trends observed

ü  Excellent written and verbal communication skills in English and French

ü  Proficiency in MS Office

ü  Good understanding of current GLP regulations and general SOPs

ü  Ability to learn quickly, meet deadlines, multitask in a challenging environment, and possess good organizational

ü  High level of attention to detail with respect to sample pretreatment procedures and raw data handling

ü  Bachelor’s degree in science (or equivalent combination of education and experience such as College with 3 years of pharmaceutical QC testing/records review experience) in Microbiology, Biochemistry, Biology, or related biological science or equivalent in job experience

ü  Previous experience in a pharmaceutical regulated Laboratory environment or pharmaceutical company is an asset

Monday to Friday 9:00 a.m. to 5:00 p.m. 

Occasionally on weekends

40 hours / week

Full-time permanent position

We offer competitive salary.