Cpv & Data Sciences Specialist

PPD (Thermo Fisher)

Whitby, Canada
Base: $69,400.00–$104,050.00; bonus/equity: not sp...
On-site
Continued process verification (cpv)
Statistical analysis
Data visualization tools
PPD (Thermo Fisher) is seeking a CPV & Data Sciences Specialist for their Whitby, Canada site, focusing on ensuring controlled and compliant manufacturing processes through data science and analytics. The ideal candidate will have at least three years of experience in pharmaceutical manufacturing and be skilled in statistical analysis and data management tools

Job Summary

  • The CPV & Data Sciences Leader ensures manufacturing processes remain consistently controlled, compliant, and continuously improving by leveraging data science and digital tools.
  • This role drives the design and execution of Continued Process Verification (CPV) programs while translating complex process data into actionable insights.
  • The position bridges manufacturing, quality, and digital teams to deliver scalable, data-driven decision-making across the process lifecycle.

Matching Summary

Match Score: 85

PPD (Thermo Fisher) is seeking a CPV & Data Sciences Specialist for their Whitby, Canada site, focusing on ensuring controlled and compliant manufacturing processes through data science and analytics. The ideal candidate will have at least three years of experience in pharmaceutical manufacturing and be skilled in statistical analysis and data management tools.

Salary

Base: $69,400.00–$104,050.00; Bonus/Equity: Not specified; Benefits: Medical, Dental, & Vision, PTO, Holidays, Retirement Savings, Tuition Reimbursement

Skills & Requirements

Must-have

  • Continued Process Verification (CPV)
  • statistical analysis
  • data visualization tools
  • Good Manufacturing Practices (GMP)
  • data integrity principles

Nice-to-have

  • AI and machine learning models
  • digital manufacturing solutions
  • cross-functional collaboration
  • continuous improvement initiatives

Key Requirements

  • Bachelor’s degree in engineering, Data Science, Statistics, Pharmaceutical Sciences, or related field
  • Minimum 3 years of experience in pharmaceutical manufacturing, MSAT, process validation, or data analytics
  • Experience applying Continued Process Verification (CPV) principles
  • Proficiency with data analytics and visualization tools
  • Knowledge of regulatory guidelines (FDA, EMA, ICH)
  • Familiarity with GMP and data integrity principles (ALCOA+)

Work Rights

Must be legally authorized to work in Canada

Tailored Resume

Cover Letter