Description :
Job Title - Process Monitoring and Data Analytics
Location - Parsippany, NJ
Hybrid - Onsite T / W / Th
Working hours : 8-4 : 30, 8 : 30-5, 9-5 : 30 type of hours (most of the team works 9-5)
Responsibilities :
- Process Engineer / Validation Engineer with having strong background in statistics, process monitoring and advanced statistical data analysis
- Strong background in statistics, process monitoring and advanced statistical data analysis.
- Apply established commercial biologics Continued Process Verification (CPV) program strategies and contribute to the CPV program of one or multiple biologics products.
- Author, review and approve CPV protocols, and 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 the resolution of investigations by 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 skills
- 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.
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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