337072BR
Jan 24, 2022
Turkey

Job Description

We are looking for a Quality Control Specialist who will be part of our Quality Control team.

Qualifications:

• University degree in Chemical Engineering or Chemistry

• Min 2-3 years of experience in related field in a pharmaceutical production environment

• Strong knowledge of cGMP and relevant GxP process

• Excellent communication skills in English

• Highly capable in interpersonal skills



Purpose:
-Manages Quality aspects & projects within area of responsibility.

-Ensures and supports overall GxP conformity & Compliance with the Novartis Quality Management Systems.



Major Accountabilities:

-Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity & eCompliance

-Support exception investigations

-Review & approval of production, QC, and AS and T records

-MBR review

-Support OpEx improvement projects Qualified Person

– Executes batch release in compliance with registration

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

Collaborating across boundaries Functional Breadth QC/ QA in pharmaceutical ind./ biotech with environmental monitoring & cleanliness zones English Quality Control (QC) Testing Knowledge of GMP Knowledge of IT Applications & tools Quality Standards Quality Assurance
Novartis Technical Operations
NTO QUALITY
Turkey
Kocaeli
Quality
Full Time
Regular
No
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337072BR

Quality Control Specialist

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