Quality Associate (m/f)

Opis posla

        - Monitoring and ensuring the implementation of Quality Assurance elements, regulatory requirements, and applicable standards in pharmaceutical manufacturing
- Coordinating and executing Quality Assurance activities related to product release procedure
- Reviewing batch documentation and ensuring compliance with cGMP requirements
- Preparing and maintaining product specifications in accordance with cGMP guidelines
- Implementing quality requirements for new products throughout project phases and during technology transfer
- Involvement in quality processes related to investigations, complaints, market actions, change controls, CAPA and MDCP CAPA systems, regulatory inspections and internal audits, risk management, projects, and technology transfer

Uvjeti:
- University degree or 300 ECTS in Chemical Technology, Biotechnology, Animal Health, Pharmacy, natural sciences or other related university
- Proficiency in Croatian and English language
- Competency in MS Office applications and the Internet
- At least 1 year of working experience is advantage
- Experience in Method 1, Veeva, SAP, EDMS, LIMS is an advantage
- Experience in Quality Assurance or pharmaceutical manufacturing is an advantage
- Strong knowledge of GMP and relevant regulatory requirements

Benefiti:
- Organized transport to and from the site
- Work with modern automated systems 
- Strong education program 
- Christmas, Easter and holiday bonus 
- Affordable meals in an on-site cafeteria 
- Opportunities for career enhancement and development 
- Yearly pay increase and bonus based on performance
- Further professional development in a supportive environment 
- Free psychotherapy and coaching sessions for employees and people close to them
- Bravo employee recognition system 
- Opportunity for working on projects with other Pfizer sites and locations 
- Free fruit and hot beverages on the site
    

Kako se prijaviti

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