QC Analyst – cGxP, Stability & Micro QC

Sandoz; Gebze; On-site; TRY 180,000 - 320,000; Full time

Job summary

Sandoz is seeking an experienced QC/QA professional in Gebze, Turkey to lead CAPA definitions, KPI trending, and stability testing activities within a GMP environment. You will review analytical data for release, support site qualification, and ensure data integrity across testing processes.

The role requires 3-5 years in pharma analytics, collaboration across boundaries, and strong knowledge of GMP standards.

Qualifications

• 3-5 years of experience in Pharma/Manufacturing analytical lab.
• GMP environment or equivalent experience.
• Collaborative work across functions.

Responsibilities

• Review and approve analytical data and tests (analytical release).
• Manage CAPA, KPI trending and data integrity reviews.
• Perform stability testing planning and evaluation.
• Support site qualification and validation activities.
• Maintain and calibrate lab equipment and plan preparation.
• Monitor microbiological testing of materials and utilities.

Skills

CAPA definition

KPI trending

cGxP compliance

Data integrity

Analytical testing

Quality control

Trend analysis

Laboratory equipment

Microbiology QC

OOS handling

Job description

Sandoz is seeking an experienced QC/QA professional in Gebze, Turkey to lead CAPA definitions, KPI trending, and stability testing activities within a GMP environment. You will review analytical data for release, support site qualification, and ensure data integrity across testing processes.

The role requires 3-5 years in pharma analytics, collaboration across boundaries, and strong knowledge of GMP standards.