Quality Control Specialist

TR11 (FCRS = TR011) Sandoz Grup Sağlık Ürünleri İlaçları Sanayi ve Ticaret A.Ş.; Gebze; On-site; TRY 30,000 - 50,000; Full time

Job summary

TR11 (FCRS = TR011) Sandoz Grup Sağlık Ürünleri İlaçları Sanayi ve Ticaret A.Ş. is seeking a laboratory professional in Gebze, Turkey. This role will utilize chemistry laboratory skills to conduct analytical testing and ensure compliance with established protocols.

Key responsibilities include sample management, analytical documentation according to GxP standards, and troubleshooting product complaints. Candidates should have strong technical knowledge and experience in the pharmaceutical or chemical laboratory environment.

Qualifications

• Sound technical & scientific knowledge of pharmaceutical/chemical industries.
• Working experience in a laboratory environment in pharmaceutical analytics/QC.

Responsibilities

• Manage sample storage and conduct analytical testing/documentation.
• Perform stability testing and manage samples according to GxP standards.
• Report technical complaints/adverse events related to products within 24 hours.

Skills

Continuous Learning

Dealing With Ambiguity

Decision Making Skills

GXP

Industry Standards

Laboratory Equipment

Laboratory Excellence

Quality Control (QC) Testing

Quality Control Sampling

Self‑Awareness

Technological Expertise

Total Quality Management

Job description

Job Summary

This role utilizes chemistry laboratory skills to test and measure product or materials while ensuring analysis is performed according to established Standard Operating Procedures (SOPs), Analytical Methods & Compendia.

Major Accountabilities

• Sample storage and management.
• Analytical testing/documentation of drug product/finished product/complaints/stability/packaging material samples to GxP standards.
• Stability – testing, sample storage and management; analytical documentation of stability samples to GxP standards.
• Reporting of technical complaints/adverse events/special case scenarios related to Sandoz products within 24 hours of receipt.
• Distribution of marketing samples (where applicable).

Key Performance Indicators

• Orders processed correctly and quickly, with no waiting times due to wrong or delayed orders.
• Deadline adherence: orders completed on time, missed deadlines reported in good time, shortest possible lead time.
• Constant readiness for inspection, with no critical complaints from superiors and inspectors.
• Consistent adherence to GMP, GSU guidelines and SOPs, with no critical irregularities.
• Finding and implementing optimization options to reduce costs.
• Completed training plan.

Minimum Requirements

• Work Experience: Sound technical & scientific knowledge of pharmaceutical/chemical, and working experience in a laboratory environment in the pharmaceutical analytics/QC/ equivalent industry.

Key Skills

• Continuous Learning
• Dealing With Ambiguity
• Decision Making Skills
• GXP
• Industry Standards
• Laboratory Equipment
• Laboratory Excellence
• Quality Control (QC) Testing
• Quality Control Sampling
• Self‑Awareness
• Technological Expertise
• Total Quality Management

Languages

English.