Sr Associate Quality

Job Description:

Responsibilities

• Navigate and execute transactions in GMP systems (Empower, LIMS, Veeva, Spotfire).
• Work closely with in the product Quality organization to drive standardization of data, and chromatographic overlay activities.
• Author and maintain GMP technical reports supporting regulatory filings within quality systems (e.g., Veeva).
• Collate, review, verify, and archive GMP data for late-stage clinical and commercial products.
• Ensure accuracy and completeness of product data with high attention to detail.
• Collaborate across global teams and time zones, effectively communicating findings and project updates.

Qualification & Experience

• Master’s degree with minimum 6 years of Pharmaceutical/Biotechnology experience in Quality, Operations, Scientific, or Manufacturing fields