The role
You will inspect finished product — the last human check before a medicine leaves the site.
What you will do
- Perform manual and automated visual inspection of filled units to standard
- Maintain inspection qualification, including periodic requalification
- Document defects accurately and route rejects correctly
- Support defect library maintenance and trending
- Escalate unusual defect patterns promptly
What success looks like at 12 months
You maintain inspection qualification without difficulty, your defect classification agrees with review, and you have flagged a trend worth investigating.
What we require
- Ability to pass and maintain vision and inspection qualification
- Sustained concentration and consistency across a shift
- Precise documentation habits
- Willingness to work a 12-hour rotating shift
What we would like, but will teach you
- Prior visual inspection experience
- GMP environment experience
- Quality control background in another regulated industry
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.
Onsite at Bloomington, IN on a 12-hour rotating shift, typically 3-on/4-off alternating with 4-on/3-off, days and nights. Shift differentials of 12–20% apply on top of base.
Pay and rewards
This role sits at grade 4, with a base range of $46,000 – $60,500 for this location, plus annual bonus, retirement contributions of up to 9%, and day-one benefits. See the full package.
About the site
Our drug product and sterile fill-finish site. 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.