Quality Control Specialist (Temp)
BR12 (FCRS = BR012) SANDOZ DO BRASIL IND FARMACEUTICA LTDA
Apply to this job 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 ManagementAbout 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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