Cleaning Validation Specialist (m/f)

Requirements

• University Degree or 300 ECTS - Biotechnology, Food Technology, Natural Sciences, Chemical Engineering and Technology
• Working knowledge of regulatory requirements and GMP standards
• Minimum 2 years of experience in cleaning process development or cleaning validation in pharmaceutical industry
• Proficiency in Croatian and English
• IT literacy (MS Office: Word, Excel, PowerPoint)
• Candidate Profile (Skills & Competencies):
• Good communication and collaboration skills
• Proactive, structured and detail-oriented approach
• Solid analytical thinking and problem-solving capabilities
• Ability to collaborate within a team environment and contribute to team effectiveness
• Accountability and reliability in execution
• Knowledge of process engineering, biochemical engineering, protein biochemistry, protein purification, chemical technology is an advantage
• What you get:
• 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 health check-ups
• Free psychotherapy and coaching sessions for employees and people close to them
• Bravo employee recognition system
• Free day in month of birth
• Opportunity for working on projects with other Pfizer sites and locations
• Free fruit and hot beverages on the site
• Insurance from accident 24/7
• Hybrid work arrangements
• Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
• To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
• Engineering

Benefits

Additional Information

(position based in Savski Marof) Short Job Description / Responsibilities: Participate in the development and implementation of cleaning strategies, cleaning processes and cleaning validation for new processes and equipment in biopharmaceutical manufacturing Support optimization and continuous improvement of existing cleaning processes Contribute to preparation of registration documentation and collaborate with regulatory authorities Provide technical expertise in cleaning validation and support cross-functional project activities Collaborate with different departments and functions (Quality, Engineering, MS&T, Operations) Support resolution of technical challenges and participate in audits and regulatory inspections Ensure compliance with GMP requirements and internal procedures

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