Job Title: CSV Lead Computer System Validation
Location: Lancaster, PA
Experience: 1O 20 Years
Job Type: Long-Term Contract
Work Model: Onsite
Job Summary:
Seeking an experienced CSV Lead to support Computer System Validation activities for a newly constructed Sterile Drug Product Clinical Manufacturing facility. The role involves leading CSV strategy, validation documentation, and execution activities in a GMP-regulated pharmaceutical environment.
Key Skills:
Computer System Validation (CSV)
AVEVA System Platform & PI Historian
Allen Bradley & Siemens PLC
SCADA, HMI, OIT Platforms
Operational Technology (OT)
Instrumentation & Control Systems
Alarm Management Systems
Robotic Isolators & Lyophilization
Autoclave & Equipment Wash Systems
Kneat Experience Preferred
Requirements:
10 20 years of CSV experience in Pharma/Biotech
Strong GMP/GxP validation knowledge
Ability to work independently in fast-paced project environment
Excellent communication and deviation management skills
Thanks
Adarsh Mallik
CENTSTONE LLC
adarsh.mallik@centstone.com
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