Quality Compliance Specialist
Istanbul, Türkiye Design / Civil engineering / Industrial engineering
Job description
Job Description
Compliance Specialist will have an oversight on QA activities;
•Involving in critical issues occurred in production,
•Handling of training system, reporting of cockpit,
•Leading GMP committee meetings,
•Leading Quality governance preparations,
•Preparing APQRs, coordinating and supervising e-PQR tool,
•Handling of quality agreements,
•Following up AQWA action status and to ensure the on time closure,
•Involving at the HA inspections and audits,
•Being IGM lead coordinator, being key user of AQWA-A,
•Leading updates of the Site Master file periodically.
Position Title
Quality Compliance Specialist
Desired profile
Minimum requirements
•University degree in Pharmaceuticals, Chemical Engineering or Chemistry
•Minimum 3 years of experience in a similar position at a multinational pharmaceutical company
•Excellent communication skills in English
•Team working and customer oriented mindset
•Knowledge of quality activities, change management system and leading meetings and projects
•Good analytical thinking and problem solving skills
•Ability to work in a fast-paced changing environment
•Detail-oriented, willing to work in a challenging environment
•No military obligation for male candidates
Job Type
Full Time
Country
Turkey
Work Location
İstanbul
Functional Area
Quality
Division
Novartis Technical Operations
Business Unit
NTO QUALITY
Employment Type
Regular
Company/Legal Entity
Novartis Turkey