Quality Control Analyst – GMP Drug Testing

Socket.dev; Hamilton; On-site; CAD 60,000 - 75,000; Full time

Benefits offered by this job

Group Health & Dental Benefits (from 1

RRSP Matching Program

Perkopolis

Employee Assistance & Wellness

Parking Allowance

Job summary

AtomVie Global Radiopharma Inc. in Hamilton, ON is seeking a QC Analyst to perform quality control testing of finished drug products, raw materials and in‑process samples in accordance with GMPs and internal SOPs.

You will generate Certificates of Analysis, test reports and data summaries, calibrate essential lab equipment, manage inventory of reagents and standards, and maintain regulatory documentation for nuclear safety and quality compliance. Shift work and weekends may be required.

Qualifications

• College Diploma or B.Sc. in Chemistry, Biotechnology, or related field.
• 1–3 years of experience in analytical chemistry techniques (HPLC, GC, TLC), microbiology tests (Endotoxins) or biology tests (ELISA, SDS-PAGE).
• Proficiency with Empower data processing software; proficiency with Excel and Word; strong written and spoken English.

Responsibilities

• Perform QC testing of finished drug products, raw materials and in‑processing testing per STMs (compendial or in‑house).
• Document data accurately and write COAs, test reports and data summaries.
• Calibrate/maintain lab equipment and manage inventory of reagents and standards.
• Maintain regulatory documentation related to nuclear safety and GMP compliance.
• Coordinate QC testing with contract labs/CROs per USP/EP; plan and complete tasks on schedule.

Skills

English communication

Team collaboration

Education

College Diploma or B.Sc. in Chemistry/Biotechnology/related

Tools

Empower (Waters HPLC)

Excel

Word

Job description

AtomVie Global Radiopharma Inc. in Hamilton, ON is seeking a QC Analyst to perform quality control testing of finished drug products, raw materials and in‑process samples in accordance with GMPs and internal SOPs.

You will generate Certificates of Analysis, test reports and data summaries, calibrate essential lab equipment, manage inventory of reagents and standards, and maintain regulatory documentation for nuclear safety and quality compliance. Shift work and weekends may be required.