QC Technician

Proven Recruiting; Oakville; On-site; CAD 50,000 - 60,000; Full time

Job summary

A biotech organization in Oakville, Ontario, seeks a QC Technician to establish and scale Quality Control processes that impact patient care. You will execute QC activities, partner with cross-functional teams, and lead investigations related to manufacturing processes. Candidates should have a Bachelor’s degree in a technical field and 5+ years of Quality Assurance experience in a cGMP environment. The position offers a salary range of CAD $50,000–$60,000, along with a diverse and inclusive workplace.

Qualifications

• 5+ years of experience in Quality Assurance within a cGMP environment.
• Hands-on experience with QC/QA processes for reagents, consumables, or IVD-related manufacturing.
• Strong communication and documentation skills.

Responsibilities

• Execute QC activities including inspections and batch record review.
• Collaborate with teams to define inspection methods and quality controls.
• Lead investigations for quality incidents related to manufacturing processes.
• Establish and improve QC processes and work instructions.

Skills

Quality Assurance in cGMP environment

QC/QA processes for reagents

Attention to detail

Communication skills

Cross-functional collaboration

Education

Bachelor’s degree in a technical field

Job description

QC Technician, Oakville, Ontario, Canada, pay is \$50,000 - \$60,000 CAD

Are you excited about building quality systems that directly impact patient care? Join an innovative biotech organization where you’ll help establish and scale Quality Control processes for reagents and consumables as the company moves from prototype through clinical and commercial manufacturing.

Who you are

• Bachelor’s degree in a technical field with 5+ years of experience in Quality Assurance within a cGMP environment
• Hands‑on experience with QC/QA processes for reagents, consumables, or IVD‑related manufacturing
• Strong attention to detail with excellent communication and documentation skills
• Proven ability to collaborate cross‑functionally across Manufacturing, Engineering, and Development teams

What you’ll do

• Execute QC activities including incoming, in‑process, and final inspections, batch record review, and product release
• Partner with Manufacturing, Engineering, and Development teams to define inspection methods, acceptance criteria, and quality controls
• Lead and support investigations including OOS, quality incidents, and CAPAs related to manufacturing processes and products
• Establish and improve QC processes, work instructions, supplier quality activities, and Materials Review Board operations

Why work here

• Play a key role in building the QC foundation for a growing biotech manufacturing operation
• Influence how products scale from early development to clinical and commercial use
• Collaborate closely with multidisciplinary teams shaping real‑world diagnostic products

Compensation

Compensation is determined by several factors which may include skillset, experience level, and education. The expected range for this role is \$50,000–\$60,000 per year CAD. Please note this range is an estimate and actual pay may vary based on qualifications and experience.

We actively support and promote people of various backgrounds, from race, religion, gender to geographical area, university, lifestyle, and personality type. Proven Recruiting is minority‑owned, majority women, and is a strong advocate for diversity and inclusion in the broader community.