Cpv & Data Sciences Specialist

Thermo Fisher Scientific UK

Whitby, Ontario, Canada
Base: $69,400.00–$104,050.00; bonus/equity: not sp...
Continued process verification (cpv) program design
Statistical analysis of manufacturing data
Power bi and discoverant dashboard development
The role drives the design and execution of Continued Process Verification (CPV) programs while translating complex process data into actionable insights to improve product quality

Job Summary

  • The role drives the design and execution of Continued Process Verification (CPV) programs while translating complex process data into actionable insights to improve product quality.
  • Candidates must possess a minimum Bachelor's degree in engineering, Data Science, Statistics, or Pharmaceutical Sciences along with at least 3 years of relevant GMP experience.
  • The position offers competitive compensation ranging from $69,400.00 to $104,050.00 with medical, dental, vision benefits effective on day one.

Matching Summary

The role drives the design and execution of Continued Process Verification (CPV) programs while translating complex process data into actionable insights to improve product quality.

Salary

Base: $69,400.00–$104,050.00; Bonus/Equity: Not specified; Benefits: Medical, Dental, Vision Day 1; Paid Time Off; Retirement Savings Plan; Tuition Reimbursement

Skills & Requirements

Must-have

  • Continued Process Verification (CPV) program design
  • Statistical analysis of manufacturing data
  • Power BI and Discoverant dashboard development
  • GMP and data integrity compliance knowledge
  • Root cause analysis for deviations and OOS
  • MES and LIMS data integration experience

Nice-to-have

  • AI and machine learning model implementation
  • Cross-functional collaboration skills
  • Mentoring team members in data analytics
  • Experience with Python or R programming
  • Strong leadership and influencing abilities

Key Requirements

  • Bachelor's degree in Engineering, Data Science, Statistics, or related field
  • Minimum 3 years experience in pharmaceutical manufacturing or MSAT
  • Proficiency in statistical tools like JMP, SAS, Python, or Minitab
  • Knowledge of FDA, EMA, and ICH regulatory guidelines
  • Legal authorization to work in Canada without sponsorship

Work Rights

Must be legally authorized to work in Canada now or in the future

Tailored Resume

Cover Letter