Impact patient care significantly as a Quality Control Specialist in a dynamic biotech environment. You'll be at the forefront of developing QC processes for critical reagents and consumables. Ideal candidates should have a Bachelor’s degree in a technical field alongside 5+ years of experience in a cGMP environment. This position demands hands-on involvement in QC/QA processes and excellent documentation skills, with a focus on cross-functional collaboration across multiple teams including Manufacturing and Engineering. Key Responsibilities:
- Perform QC activities and batch record reviews
- Partner with teams to establish quality controls
- Manage investigations for OOS issues and CAPAs
- Enhance and document QC processes and work methods
- Engage with multidisciplinary teams during product development Requirements:
- Bachelor’s degree in a relevant technical field
- Over 5 years in Quality Assurance roles
- Expertise in QC/QA for reagents or IVD manufacturing
- Robust communication and detailed documentation skills
- Ability to work collaboratively across teams Elevate the quality processes that directly enhance patient outcomes and product effectiveness. #J-18808-Ljbffr

📌 Quality Control Specialist In Biotech (Oakville)
🏢 Proven Recruiting
📍 Oakville