What are the responsibilities and job description for the GMP Manufacturing System Administrator position at KBI Biopharma?
Position Summary
The “GMP Systems Administrator” supports KBI Biopharma’s Process Development and manufacturing activities by owning and supporting enterprise applications that improve KBI’s ability to execute for our customers. They will be experienced with shop floor automation and operational data management to meet KBI’s expanding data management needs and accelerate our digital transformation. The System Product Owner will work with internal and external parties to define requirements for new functionality and provide technical direction and expertise for providing that functionality. Additionally, they will have a good understanding of biopharmaceutical processing and development within a regulated environment.
What you’ll do :
- Monitor and maintain assigned application(s) in their proper operating condition to meet business requirements.
- Build, prioritize and maintain a backlog of product features / improvements. Ensure constant clarity in terms of what is to be executed next by the development / configuration team.
- Identify, develop, and deploy upgrades to improve operational efficiency and business processes.
- Provide escalated support, and manage vendor support, for assigned applications.
- Stay current on training and administration of SOPs and training activities as part of operating in a validated environment.
- Support the product's deployment to end-users. Collect end-user and other stakeholder's feedback and alter the product's roadmap to take their feedback into account.
- Develop (if needed) and manage user training for product use / access, if applicable.
- Communicate information that is valuable to the intended audience.
- Translate business needs into actionable requirements.
- Lead and provide direction for operational activities as well as project-based support.
- Provide technical expertise in the assigned software applications.
What you’ll have :
