The role
You will support the validated systems the regulated business runs on — keeping them working, compliant and genuinely useful.
What you will do
- Support and administer GxP applications used in manufacturing, quality or clinical
- Manage system change control, testing and documentation
- Troubleshoot user and integration issues
- Support periodic review, audits and inspections
- Train users and improve how systems are actually used
What success looks like at 12 months
Systems are stable and changes go through cleanly, users get answers quickly, and periodic review passes without findings.
What we require
- Experience supporting business applications, ideally in a regulated environment
- Understanding of change control and validation concepts
- Practical troubleshooting ability
- Clear communication with non-technical users
What we would like, but will teach you
- MES, LIMS, QMS or EDC system experience
- CSV experience
- Military IT or communications background
If you meet the required list, apply. We cap the preferred list at four items on purpose, and we would rather read an application from someone who is 70% there and hungry.
Military IT and communications backgrounds are a good fit for this role.
Hybrid — onsite at Research Triangle Park, NC three days a week (Tuesday, Wednesday and one team-chosen day).
Pay and rewards
This role sits at grade 7, with a base range of $89,000 – $114,500 for this location, plus annual bonus, retirement contributions of up to 9%, and day-one benefits. See the full package.
About the site
Our clinical development and digital hub. More about our locations.
Accommodations
Need an adjustment to apply or interview? Email accommodations@ingenbiotech.example. It goes to a separate team and is never shared with the hiring manager. What we can arrange.
Applications are not enabled on this demonstration site
On a live InGen careers site this button would open a one-page application: a CV and three short questions, about twelve minutes, no account required and no cover letter.