Global Quality Compliance Expert - Sterile Manufacturing

Sun Pharmaceutical Industries Ltd; Princeton (NJ); On-site; USD 101,000 - 113,000; Full time

Benefits offered by this job

Medical, dental and vision coverage

Life insurance

Disability insurance

401(k) savings plan

Flexible spending accounts

Employee assistance program

Paid time off

Job summary

Sun Pharmaceutical Industries Ltd is seeking an experienced QA professional to manage batch review of sterile and OSD manufacturing/packaging records, certificates of analysis, and related documentation in a GMP environment. The role emphasizes expert-level manufacturing investigations from FDA-approved facilities with sterile and OSD products.

The position is an individual contributor role focused on QA SME activities, with responsibility for documentation compliance, equipment qualification

Qualifications

• Thorough understanding of GMPs, specifically good documentation practices.

Responsibilities

• Lead the review of sterile and OSD manufacturing/packaging records from a Global Quality perspective.

Skills

GMP knowledge

Documentation review

QA expertise

English communication

MS Word

MS Excel

Project management

Education

Bachelor's degree

Tools

TrackWise

LMS

MS Office

Acrobat Reader

Job description

Sun Pharmaceutical Industries Ltd is seeking an experienced QA professional to manage batch review of sterile and OSD manufacturing/packaging records, certificates of analysis, and related documentation in a GMP environment. The role emphasizes expert-level manufacturing investigations from FDA-approved facilities with sterile and OSD products.

The position is an individual contributor role focused on QA SME activities, with responsibility for documentation compliance, equipment qualification