CareerPlan

QC Specialist III-Stability

US - Portsmouth, NHFull-time2026-10-05 → 2026-11-11
On-site

Core

Manage stability studies from setup through final reporting in a GMP environment to support the delivery of life-changing therapies.

Role type

Senior IC Quality Control Specialist (Stability)

Builds

Stability study reports and GMP documentation

Domain

Pharmaceutical/Biotechnology - Stability Testing

Required skills

GMP-regulated environment experience, stability protocol development and review, controlled documentation management, sample management, cross-functional collaboration, investigation support, change control support

Preferred skills

Quality Control experience, Stability experience, regulated laboratory environment experience

Responsibilities

Manage stability studies from setup through completion, Partner with customers as primary stability contact, Develop and maintain stability protocols and reports, Coordinate testing activities and sample management, Support investigations and change controls, Mentor colleagues on stability best practices