Validation Engineer - II - Integrated Resources, Inc
Parsippany, NJ 07054
About the Job
Job Title: Validation Engineer - II
Job Location: Parsippany, NJ (Hybrid role)
Job Duration: 6 Months (Possible extension)
Hybrid - Onsite T/W/Th
Working hours: 8-4:30, 8:30-5, 9-5:30 type of hours (most of team works 9-5)
Job Description:
Knowledge and Skills:
Education and Work Experience Requirements:
• 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.
Job Location: Parsippany, NJ (Hybrid role)
Job Duration: 6 Months (Possible extension)
Hybrid - Onsite T/W/Th
Working hours: 8-4:30, 8:30-5, 9-5:30 type of hours (most of team works 9-5)
Job Description:
- 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.
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 Requirements:
- 4+ 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.
• 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.
Source : Integrated Resources, Inc
