Systems Administrator (GMP, CFR Part 11) (Paid re-lo to Baltimore)
Full Time
Philadelphia, PA
Posted
Job description
- This role is on-site 2-3 days/week in Baltimore.
- Relocation assistance provided!
Responsibilities
Identify computerized needs for new systems, upgrades, and decommissioning.
Coordinate and create data flow process models and system configuration documents.
Author documentation such as procedures, summary reports, and status reports related to the data integrity projects.
Project Management of data integrity activities.
Supports risk assessments.
Function as system administrator for computerized systems.
Requirements
4+ years’ experience with data integrity and computer system compliance with 21 CFR Part 11 in a GMP pharma environment.
Strong understanding of laboratory operations, computer system validation, GAMP, and risk management.
To apply please send your application to mschroeder@thedenzelgroup.com
#IND1
data integrity, specialist, analyst, administrator, engineer, 21 CFR part 11, GMP, computer, IT
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