Sr Associate Deviation Analyst
On-site · Juncos, Juncos, Puerto Rico
Job Summary
Sr Associate Deviation Analyst role focused on deviation management within GMP/GxP. Responsibilities include cross-functional coordination across departments, facilitating communication between units and vendors to integrate information systems, leading cross-functional meetings to develop solutions, conducting impact analyses for new products and system changes, evaluating business processes for feasibility, maintaining positive relationships with managers and staff, understanding client business processes, ensuring system functionality meets requirements, and preparing complex project documentation. Requires a Bachelor's degree and 2 years in a regulated environment, bilingual in English and Spanish, and Project Management skills. Shift is administrative as needed.
Required Qualifications
- Bachelor's Degree
- 2 years of experience as a Scientist within the pharmaceutical or regulated industry
- Bilingual English & Spanish
- Project Management skills
- Experience in Deviation management within GMP/GxP environment
- Investigation lifecycle from initiation through closure
- Computerized manufacturing systems experience (MES, Veeva, SAP, PCS, or PI Historian)
Apply with one swipe on Sorce. We auto-fill applications and apply on your behalf — no cover letters, no 40-minute forms.
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.