Impact patient care significantly as a Quality Control Specialist in a dynamic biotech setting. 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 reviewsPartner with teams to establish quality controlsManage investigations for OOS issues and CAPAsEnhance and document QC processes and work methodsEngage with multidisciplinary teams during product developmentRequirements:Bachelor's degree in a relevant technical fieldOver 5 years in Quality Assurance rolesExpertise in QC/QA for reagents or IVD manufacturingStrong communication and detailed documentation skillsAbility to work collaboratively across teamsElevate the quality processes that directly enhance patient outcomes and product effectiveness.

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