Title: Stability Associate
Duration: 6 Months (Temp to perm)
Location: Waltham, MA. 02451
Position Summary:
- Support operational and technical aspects of clinical/commercial drug substance, drug product, reference standard, and placebo GMP stability programs.
- Ensure compliance and support of company Standards, Practices, and SOPs as well as ICH and FDA guidelines.
- This includes design of stability protocols, expiry dating for clinical/commercial products, providing stability sections for regulatory submissions, technical assessment of stability data, specification changes and investigations, routinely working with CMO/CLOs to ensure timelines are met for release and stability testing of product.
Key Responsibilities:
- Designs and manages studies. Collaborates with CLOs to ensure proper testing and reporting of stability samples.
- Assigns expiry to drug substance, drug product, and reference standard
- Trends and evaluates stability data proactively.
- Authors’ stability reports for regulatory submissions.
- Participates in meetings and contributes toward the goals of the CMC. Contributes to major/critical manufacturing and leads stability investigations (deviations, OOS, cross-site and cross-functional).
- Authors stability assessments writing for basic Anomalous Results (ARs) and Out of Trend (OOT) stability results.