Cleaning Validation Specialist — GMP Compliance & QA Impact

Teva Pharmaceuticals; Whitchurch-Stouffville; On-site; CAD 67,000 - 84,000; Full time

Benefits offered by this job

Health & Dental benefits

Disability & Life Insurance

Retirement Savings Program

Job summary

Teva Canada is seeking a detail-oriented Cleaning Validation Specialist for a 12-month contract in Stouffville, Ontario. You will support validation studies, coordinate sampling, and ensure GMP-compliant documentation across QA, QC, and Operations teams.

Requirements include a BSc/engineering field and 1–3 years in pharma/manufacturing, with strong data review, risk assessment, and regulatory knowledge. Travel to Teva sites may be required.

Qualifications

• Bachelor's degree in Science, Engineering, Pharmacy, or a related discipline.
• 1 to 3 years of relevant experience in pharma/biotech or regulated manufacturing.
• Knowledge of cleaning validation principles, GMP regulations, and pharmaceutical processes.

Responsibilities

• Assist in the preparation, execution, and reporting of cleaning validation studies.
• Coordinate equipment swabbing and rinse sampling activities.
• Review and organize cleaning validation data and assess against acceptance criteria.
• Prepare validation protocols, reports, risk assessments, and related documentation.

Skills

GMP knowledge

Attention to detail

Cross-functional collaboration

Analytical mindset

Time management

Education

Bachelor's degree in Science or Engineering

Tools

LIMS

Veeva

TrackWise

MS Office

Job description

Teva Canada is seeking a detail-oriented Cleaning Validation Specialist for a 12-month contract in Stouffville, Ontario. You will support validation studies, coordinate sampling, and ensure GMP-compliant documentation across QA, QC, and Operations teams.

Requirements include a BSc/engineering field and 1–3 years in pharma/manufacturing, with strong data review, risk assessment, and regulatory knowledge. Travel to Teva sites may be required.