Explore a rewarding career as a Quality Control Analyst with AtomVie, focusing on drug quality and compliance testing. Utilize your analytical chemistry skills in a dynamic GMP environment.
In this vital role, you will perform essential quality control testing and support the development of AtomVie's drug portfolio. You will document results, follow SOPs, and assist in ensuring compliance with Canadian Nuclear Safety regulations. This position is crucial for both existing products and future innovations.
Key Responsibilities:
- Execute quality control tests on pharmaceuticals and raw materials
- Document findings and generate analytical reports
- Raise issues regarding testing non-conformances
- Maintain stock of laboratory reagents and consumables
- Liaise with management for training and compliance
Requirements:
- Degree in Chemistry or Biotechnology
- 1-3 years' experience in analytical chemistry techniques
- Proficient in Empower software and Office Suite
- Team player with good communication skills
- Capability to lift up to 23 kilograms and work shifts
Join AtomVie and contribute to the science of drug safety and quality.
AtomVie Quality Control Analyst Opening in Hamilton employer: AtomVie Global Radiopharma Inc.
At AtomVie Global Radiopharma, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. As the Director of Quality Assurance, you will not only lead critical quality initiatives but also benefit from our commitment to employee growth through continuous training and development opportunities. Located in a dynamic environment, our team is dedicated to making a meaningful impact on patient lives while enjoying a supportive workplace that values excellence and integrity.
Contact Details:
AtomVie Global Radiopharma Inc. Recruitment Team
