Impact patient care significantly as a Quality Control Specialist in a energetic 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 workplace. 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 (Canada)
🏢 Proven Recruiting
📍 Canada