Short Job Description/Responsibilities:
- 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
Qualifications:
- 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
Ideal candidate's profile:
- Excellent interpersonal and communication skills
- Experience in teamwork and ability to collaborate effectively with cross‑functional departments
- Accountable, adaptable, systematic, and punctual in daily work tasks
- Strong attention to detail, analytical thinking, and problem‑solving abilities
- Ability to work independently and manage multiple priorities
What you get:
- Organiz e d transport to and from the site
- Work with mod e rn automat e d syst e ms
- Strong e ducation program
- Christmas, E ast e r and holiday bonus
- Affordable m e als in an on-sit e caf e t e ria
- Opportuniti e s for car e e r e nhanc e m e nt and d e v e lopm e nt
- Yearly pay incr e as e and bonus based on performance
- Furth e r prof e ssional d e v e lopm e nt in a supportive e nvironm e nt
- Free psychotherapy and coaching sessions for employees and people close to them
- Bravo employee r e cognition syst e m
- Opportunity for working on proj e cts with oth e r Pfiz e r sit e s and locations
- Free fruit and hot beverages on the site
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control
Top Skills
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
Gallery
Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.







