Cleaning Validation Specialist - 12-Month Contract

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

Benefits offered by this job

Health insurance

Dental

Disability insurance

Life Insurance

Employee Assistance Program

Retirement Savings

ESPP

Paid time off

Education assistance

Recognition programs

Employee discounts

Job summary

Teva Canada is seeking a detail-oriented Cleaning Validation Specialist to join our team in Stouffville, Ontario, on a 12-month contract. You will support cleaning validation activities to ensure cGMP compliance and collaborate across QA, QC, Operations, Engineering, and MS&T to maintain validated processes.

You will prepare protocols and reports, review data, and help with risk assessments and investigations while ensuring audit-ready documentation and adherence to regulatory standards.

Qualifications

• Bachelor's degree in Science, Engineering, Pharmacy, or related discipline.
• 1–3 years in pharma/biotech industries.
• Knowledge of cleaning validation, GMP and regulatory standards.
• Familiarity with Canada/US/EU regulatory requirements (GMP/GLP).
• Experience with validation documentation, CAPAs, and change controls.
• Proficiency with MS Office and quality systems (LIMS, Veeva, TrackWise, Knowledge Tree).

Responsibilities

• Assist in preparing, executing, and reporting cleaning validation studies.
• Coordinate equipment swabbing and rinse sampling activities.
• Review and organize cleaning validation data.
• Evaluate results against acceptance criteria.
• Support validation program periodic reviews and documentation.

Skills

GMP knowledge

Analytical mindset

Attention to detail

Communication skills

Team collaboration

Regulatory knowledge (Canada/US/EU)

Travel willingness

Education

Bachelor's degree in Science/Engineering/Pharmacy

Tools

LIMS

Veeva

TrackWise

Knowledge Tree

MS Excel

Job description

Teva Canada is seeking a detail-oriented Cleaning Validation Specialist to join our team in Stouffville, Ontario, on a 12-month contract. You will support cleaning validation activities to ensure cGMP compliance and collaborate across QA, QC, Operations, Engineering, and MS&T to maintain validated processes.

You will prepare protocols and reports, review data, and help with risk assessments and investigations while ensuring audit-ready documentation and adherence to regulatory standards.