Pfizer
Biopharmaceutical Manufacturing
CleaningValidationSpecialist(m/f)
Neural analysis suggests this role is
optimal for Mid candidates.
“Cleaning Validation Specialist (m/f) at Pfizer. Skills: Cleaning validation, Process optimization. Participate in development of cleaning strategies. Participate in implementation of cleaning strategies”
Industry & Context.
Problem-solving capabilities
Organized transport to site, Organized transport from site
What They're Looking For.
Must Have
University Degree or 300 ECTS, Working knowledge of regulatory requirements, Working knowledge of GMP standards, Minimum 2 years of experience, Proficiency in Croatian, Proficiency in English, IT literacy (MS Office)
Nice to Have
Knowledge of process engineering, Knowledge of biochemical engineering, Knowledge of protein biochemistry, Knowledge of protein purification, Knowledge of chemical technology
What You'll Do.
Participate in development of cleaning strategies
Participate in implementation of cleaning strategies
Participate in development of cleaning processes
Participate in implementation of cleaning processes
Participate in development of cleaning validation
Participate in implementation of cleaning validation
Support optimization of existing cleaning processes
Support continuous improvement of existing cleaning processes
Contribute to preparation of registration documentation
Provide technical expertise in cleaning validation
Support cross-functional project activities
Collaborate with different departments
Collaborate with different functions
Support resolution of technical challenges
Participate in audits
Participate in regulatory inspections
Ensure compliance with GMP requirements
Ensure compliance with internal procedures
How You'll Work.
Team & Collaboration
Cross-functional project activities; Quality department; Engineering department; MS&T department; Operations department
Full Job Description
_(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 **Qualifications:** * 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
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