Stability Program Lead — FDA-Regulated Pharma

Hikma Pharmaceuticals; Bedford (OH); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Annual performance bonus

401(k) program with match

Paid time off 20 days

Parental leave

Comprehensive health benefits

Employee discount program

Job summary

Hikma Pharmaceuticals USA Inc. is seeking a Stability Administrator to coordinate stability programs for oral and sterile injectable products, ensuring compliance with ICH, FDA, and cGMP requirements.

You will manage sample lifecycle, data integrity, and inspection readiness in regulated manufacturing environments. The role involves cross-functional collaboration with QC, QA, Regulatory Affairs, and Manufacturing to support stability studies, regulatory submissions, and lifecycle management,

Job description

Hikma Pharmaceuticals USA Inc. is seeking a Stability Administrator to coordinate stability programs for oral and sterile injectable products, ensuring compliance with ICH, FDA, and cGMP requirements.

You will manage sample lifecycle, data integrity, and inspection readiness in regulated manufacturing environments. The role involves cross-functional collaboration with QC, QA, Regulatory Affairs, and Manufacturing to support stability studies, regulatory submissions, and lifecycle management,