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.

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