Regulatory Affairs Project Manager (m/f/d)

Deep understanding of global healthcare regulatory frameworks and compliance requirementsAbility to develop and execute regulatory strategies for complex products and submissionsStrong expertise in managing product registration dossiers and regulatory documentationExcellent stakeholder management and relationship-building skills across internal and external partnersAbility to influence, communicate effectively and drive alignment without direct authorityIndependent decision-making combined with sound judgment in complex situationsStrong innovation mindset with a focus on continuous improvement and digitalizationAdvanced problem-solving skills with the ability to identify and implement effective solutionsAgile mindset with a willingness to embrace change, simplify processes and increase productivityStrong collaboration skills with the ability to bring teams together and achieve common goals Bachelor's or Master's degree in Life Sciences, Data Science, or a related field, alternatively equivalent technical or laboratory qualificationExperience in Regulatory Affairs, R&D, Quality, Operations, Clinical Affairs, or a related healthcare environmentExperience in healthcare regulatory affairs and regulatory compliance activitiesAbility to manage complex projects and navigate challenging regulatory requirements independentlyStrong understanding of regulatory submission processes and product registration activitiesFluent English communication skills, both written and spokenSelf-driven and able to work independently with minimal supervisionConfident in collaborating with cross-functional stakeholders, including R&D, QC, Operations, and international Regulatory Affairs teamsStrong organizational, communication, and stakeholder management skillsAbility to prioritize, solve problems effectively, and deliver results in a global regulatory environment 30 days leave per yearA highly motivated team and an open way of communicationA very renowned companySupport throughout the entire application process With over 15 years of experience in the pharmaceutical and chemical industry as well as in biotechnology and medical engineering, we know the key contacts at companies that are recruiting for challenging jobs with real potential. The current high demand for staff has opened up exciting opportunities for dedicated experts who want to develop professionally and to further their careers. As recruitment specialists with an international network of contacts, we can offer you decisive advantages – completely free of charge. Register with us and reap the benefits of interesting job offers that match your skills and experience.

Responsibilities

Deep understanding of global healthcare regulatory frameworks and compliance requirementsAbility to develop and execute regulatory strategies for complex products and submissionsStrong expertise in managing product registration dossiers and regulatory documentationExcellent stakeholder management and relationship-building skills across internal and external partnersAbility to influence, communicate effectively and drive alignment without direct authorityIndependent decision-making combined with sound judgment in complex situationsStrong innovation mindset with a focus on continuous improvement and digitalizationAdvanced problem-solving skills with the ability to identify and implement effective solutionsAgile mindset with a willingness to embrace change, simplify processes and increase productivityStrong collaboration skills with the ability to bring teams together and achieve common goals

Benefits

30 days leave per yearA highly motivated team and an open way of communicationA very renowned companySupport throughout the entire application process