Demo

Validation Engineer - II

ATR International
Santa Clara, CA Full Time
POSTED ON 1/17/2025 CLOSED ON 4/15/2025

What are the responsibilities and job description for the Validation Engineer - II position at ATR International?

Job Description :

We are seeking a Validation Engineer - II for a very important client.Responsibilities :

  • Strong background in statistics, process monitoring and advanced statistical data analysis.
  • Apply established commercial biologics Continued Process Verification (CPV) program strategies and contribute to CPV program of one or multiple biologics products.
  • Author, review and approve CPV protocols, reports and present CPV data as needed to Subject Matter Experts (SMEs).
  • Support batch processing data collection and verification activities.
  • Identifies and implements improvements for data collection and management to enable quick and reliable data analysis.
  • Provides statistical expertise for all global commercial process monitoring in compliance with current ICH / Health Authority, QbD guidelines and SOPs.
  • Assist in resolution of investigations doing statistical analysis.
  • Works on moderately complex problems where analysis of situations or data requires an in-depth evaluation of various factors.
  • Exercises judgment within generally defined practices and policies in selecting statistical methods, techniques and evaluation criteria for obtaining results.

Requirement :

The ideal candidate should possess the following qualifications : Knowledge and Skills

  • Experience with optimization and statistical data analysis tools such as Minitab, JMP, Spotfire and R Basic programming in R and Python preferred
  • Excellent technical writing skill
  • Working knowledge of GMP and regulatory requirements of biopharmaceutical manufacturing is preferred
  • Excellent troubleshooting skills and ability to solve complex technical issues.
  • Understanding of guidelines required by FDA, EMA, and other regulatory bodies
  • Extensive knowledge of industry practices.
  • Excellent verbal, written, and interpersonal communication skills are required.
  • Ability to effectively manage multiple projects / priorities. Education and Work Experience Requirements4 years of relevant experience and a BS degree in a relevant scientific discipline.2 years of relevant experience and an MS degree in a relevant scientific discipline. Must Have :
  • Strong background in statistics, process monitoring and advanced statistical data analysis.
  • Apply established commercial biologics Continued Process Verification (CPV) program strategies and contribute to CPV program of one or multiple biologics products.
  • Support batch processing data collection and verification activities.
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