A leading global pharmaceutical company with a facility in Wilson NC is in immediate need of a Terminal Sterilization Engineer to join their team on a 9-month project (possible extension). This role is fully onsite in North Carolina.
The Terminal Sterilization Engineer has strong experience in sterilizing pharmaceutical products manufactured through automated systems. This role will primarily focus on hands-on sterilization validation engineering specifically for IV bags and potentially other similar finished products.
Key Responsibilities:
Lead and execute sterilization validation activities for terminally sterilized products
Develop and optimize sterilization cycles (cycle development)
Author and review validation documentation including protocols and final reports
Support execution of validation runs and provide technical guidance on data evaluation
Collaborate with cross-functional teams to ensure compliance with regulatory and quality standards
Top Requirements:
Bachelors degree (minimum required)
5 years of sterilization engineering experience within pharmaceutical manufacturing
Aseptic manufacturing experience
Strong expertise in sterilization validation including documentation and report generation
Experience with cycle development
Strong background in terminal sterilization specifically water shower sterilization
Experience with finished products such as IV bags preferred
A leading global pharmaceutical company with a facility in Wilson NC is in immediate need of a Terminal Sterilization Engineer to join their team on a 9-month project (possible extension). This role is fully onsite in North Carolina. The Terminal Sterilization Engineer has strong exper...
A leading global pharmaceutical company with a facility in Wilson NC is in immediate need of a Terminal Sterilization Engineer to join their team on a 9-month project (possible extension). This role is fully onsite in North Carolina.
The Terminal Sterilization Engineer has strong experience in sterilizing pharmaceutical products manufactured through automated systems. This role will primarily focus on hands-on sterilization validation engineering specifically for IV bags and potentially other similar finished products.
Key Responsibilities:
Lead and execute sterilization validation activities for terminally sterilized products
Develop and optimize sterilization cycles (cycle development)
Author and review validation documentation including protocols and final reports
Support execution of validation runs and provide technical guidance on data evaluation
Collaborate with cross-functional teams to ensure compliance with regulatory and quality standards
Top Requirements:
Bachelors degree (minimum required)
5 years of sterilization engineering experience within pharmaceutical manufacturing
Aseptic manufacturing experience
Strong expertise in sterilization validation including documentation and report generation
Experience with cycle development
Strong background in terminal sterilization specifically water shower sterilization
Experience with finished products such as IV bags preferred