Quality Control Specialist (Temp)

BR12 (FCRS = BR012) SANDOZ DO BRASIL IND FARMACEUTICA LTDA

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Gebze (Sandoz) Until 9/11/2026 3+ years exp First posted July 13, 2026 Last posted July 13, 2026
Job description

Job Description Summary

-Highly skilled and experienced laboratory professional who contributes by performing analytical release testing, investigational support, research support, and stability testing.

Job Description

Major accountabilities: 

  • OOx/Deviation handling.
  • CAPA definition -KPI trending -Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) Stability -Stability testing (Projects) – protocol preparation, evaluation, report preparation.
  • Reporting (Stability plan preparation, trend analysis, evaluation) -Performance of Stability studies, protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release) -Microbiological QC -Perform Microbiological testing of materials and utilities, environmental and personnel monitoring -Provide expert Support for site qualification and validation activities -Maintain and calibrate equipment incl. plan preparation -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -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:

  • The relevant KPIs that are defined in the Quality Control areas apply: e.g. analytical lead times -Timely and GMP-compliant analysis & documentation of the results.
  • Error rate: Number of OOS (analysis errors) related to the number of analyzes -No complaints about official inspections.
  • Individual performance is assessed using the PMP performance dialog together with the manager  

Minimum Requirements: 
Work Experience:

  • Functional Breadth.
  • 3-5years experience in Pharma/Manufacturing sector in analytical lab in.
  • Collaborating across boundaries.
  • A GMP environment/equivalent.

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.

Skills Desired

Continued 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
About this role

Summary

Perform analytical testing, stability studies, investigations, and ensure GMP compliance in pharma QC lab.

Job title

Quality Control Specialist (Temp)

Experience level

3-5 years

Minimum experience

3+ years exp

Industry

pharmaceuticals

Location requirements

Gebze, Turkey; remote work not specified

Salary

Not specified

Management role

No

Skills & keywords

Required skills

Gxplaboratory equipmentquality control testingquality control samplingtotal quality management

Preferred skills

continued learningdealing with ambiguitydecision making skillsindustry standardslaboratory excellenceself-awarenesstechnological expertise

Specializations

QC testingMicrobiologicalstability testingGxPlab equipment
Locations

Structured locations inferred from the posting.

Gebze, Kocaeli, Türkiye

Work arrangement unknown City
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