Pharmaceutical quality investigations specialists apply root-cause analysis and CAPA expertise in an office-based Sun Pharma role with regular hours.
As Specialist, Quality (Investigations), you help ensure pharmaceutical products meet GMP, Company requirements, and regulatory expectations. The work centers on deviation investigations, risk assessments, CAPA effectiveness, and non-conformance resolution. You also support quality systems, certification activities, and audits.
Key Responsibilities: Prepare deviation investigation reports
Identify root causes and complete associated risk assessments
Manage non-conformance investigations within required timelines
Assess CAPA effectiveness and execute associated actions
Participate in internal, customer,



and regulatory audits
Requirements: Bachelor's Degree in Science or related discipline
Minimum one year pharmaceutical Quality Assurance, Quality Control, or Manufacturing experience
Working knowledge of pharmaceutical Quality Systems
Knowledge of pharmaceutical standards, validation, and transfer requirements
Experience with TrackWise, LMS, EDMS, or SAP is an asset
Bring pharmaceutical quality systems knowledge, investigation discipline, and CAPA expertise to Sun Pharma’s quality organization.

#J-18808-Ljbffr

📌 Pharmaceutical Quality Investigations Specialist (Ontario)
🏢 Sun Pharmaceutical Industries
📍 Ontario