Quality Specialist (m/f)

Work location: Savski MarofWhat You Will AchieveYou will be an integral member of Pfizer’s Quality Systems organization, contributing to a strong and effective Quality management framework. In this role, you will be responsible for the governance, oversight, and continuous improvement of core Quality Systems, including Change Control, Documentation Management, Quality Risk Management, Supplier Quality Management, Quality Management Review processes, Quality Plan & Quality Policy.You will ensure that these systems are robust, compliant, and aligned with regulatory requirements and Pfizer global standards. Your work will support cross‑functional teams by enabling effective change implementation, clear and controlled documentation, risk‑based decision‑making, and transparent management oversight. Through these activities, you will help drive quality strategy, performance metrics, and site quality objectives.As a Quality Specialist, you will apply your expertise and judgment to support team goals and deliver critical quality outcomes. Your ability to communicate clearly, collaborate across functions, and use effective quality tools will help resolve complex issues and build alignment among stakeholders.Your commitment, attention to detail, and focus on continuous improvement will strengthen Pfizer’s Quality Systems and help ensure the reliable supply of high‑quality medicines for patients around the world.How You Will Achieve ItContribute to the successful delivery of complex Quality Systems activities by effectively managing your time, meeting agreed targets, and planning work for assigned projects within a collaborative team environment.Review, interpret, and trend quality metrics, providing input to action plans required to maintain or enhance compliance across Quality Systems.Support Quality Risk Assessments to enable risk‑based decision‑making across systems and processes.Ensure Quality Systems remain compliant, inspection‑ready, and aligned with global regulatory and Pfizer requirements.Support Quality Management Review activities by ensuring accurate, complete, and timely updates of quality data.Support Supplier Quality activities, including participation in supplier qualification programs and ongoing supplier oversight.Ensure timely follow‑up and closure of corrective and preventive actions arising from internal audits, regulatory inspections, supplier management activities, and other Quality Systems processes.Collaborate with cross‑functional and group engagement teams to evaluate Quality Systems performance and recommend improvements to processes, equipment, and laboratory or operational practices.QualificationsMust-HaveBachelor's Degree 3+ years' experience in pharmaceutical industryStrong interpersonal skills to provide trainingExcellent organizational skills, ability to handle changing deadlines and responsibilities.Strong written and verbal communication skillsStrong computer knowledge (MS Office Suite)Nice-to-HaveDemonstrated ability to learn and master new applications softwareExperienced in auditing with Good Manufacturing Practices (also cGMP) regulated industriesWhat we offer: Organized transport to and from the site Hybrid work arrangementsWork 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  Opportunity for working on projects with other Pfizer sites 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. Pfizer endeavors to make www.pfizer.com/careers accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process and/or interviewing, please email disabilityrecruitment@pfizer.com. This is to be used solely for accommodation requests with respect to the accessibility of our website, online application process and/or interviewing. Requests for any other reason will not be returned. 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. Quality Assurance and Control