.. of open orders Carrying out business trips Our requirements Active sales experience in B2B; Willingness to make decisions and responsibility for the result; High self-motivation to work and development; English and German at a communicative level is a must Well-developed communication skills, ability .. inny
At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All . We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone , we are the people behind the brands you trust. We are Opill, Compeed, Solpadeine, NiQuitin, ACO, and many more. We Are Perrigo . We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging. Join us on our One Perrigo journey as we evolve to a blended-branded business to win in self-care. Description Overview Perrigo are bringing an exciting new proposition to the Warsaw market and we would love to hear from experienced CMC regulatory affairs Project managers. Help us lay the foundations of our new Business Services Centre based in Mokotów. We need a diverse group of action-oriented colleagues who have the desire to go beyond the transactional elements of their role and be part of building something truly special! Join a collaborative, international environment with many cross-functional interactions and opportunities. Build your career in a Global organisation with opportunities for career growth and supported learning. Thrive from a trust-based leadership approach that encourages innovation and transparent communication. Access extensive training and development platforms, including our internal GROWyou program, to support continuous learning, skill development, and professional advancement. See your talents recognised and rewarded through extended responsibilities and varied career move opportunities ***We currently offer a hybrid working pattern with 3 days in the office and 2 days working remotely. Scope of the Role Lead CMC Regulatory Affairs Projects; providing updates to business and reporting against project plans Develop regulatory strategies for CMC (chemistry Manufacturing & control) aspects of new MAAs( including Responses to HA questions), New Product Development projects, and life cycle maintenance activities Complete due diligence on time for any assigned product dossiers, identifying risks and opportunities Identify risks and opportunities for assigned projects Support the technical team and provide any scientific expertise to define the development or validation plan for assigned projects Review technical documentation generated by the site during the development project or validation of the site transfer in particular protocols and development reports, validation of processes and analytical methods, test methods and specifications and stability protocol and reports Support Change Controls – providing RA assessment, strategy and appropriate actions Manage, coordinate, write and maintain technical part/quality ( CMC ) part of CMC dossiers (e.g complex MA Variations such as Site Transfer and Reformulation projects) Responsibility of CMC submission to ensure continuity of supply and new products meet submission timeline Support project team to resolve regulatory issues with Health Authorities Support resolution and action related to artwork related issues CMC support for MDR related changes to the medicinal CTD CMC expertise and RA activity in support of emerging ingredient issues in compliance with related guidance Play an active role in quality management of product by providing expertise in managing request for changes , preparing annual product quality review and any matters related to product quality control Develop, roll out and maintain relevant internal procedures and best practices Maintain the integrity of regulatory data in the relevant databases Interpret and implement legislation, follow changes in national regulations and legislations and proactively manage impact of these changes Experience Required Minimum Qualification University Degree or equivalent scientific qualification Minimum of 7 years of relevant work experience (preferably in CMC Regulatory Affairs or R&D), with a practical experience of working with at least one of the specific product types, a background knowledge of healthcare products (e.g. medicines, medical devices, cosmetics) Minimum Work Experience Must have strong experience in CMC and pharmaceutical life cycle management. Must have experience in due diligence of the CMC dossiers ( 3.2.P and 3.2.S) Desirable to have experience in project management Desirable to have experience in Nitrosamines project management Person Profile Self-motivated, flexible and open to changing requirements Ability to work effectively, both autonomously and in teams Good interaction skills with internal and external stakeholders. Ability to handle multiple complex projects in parallel, with high accuracy and attention to detail Highly driven with enthusiasm to meet requirements and cope under demanding pressure Profound organizational and problem-solving skills Solid communicator in English. Additional language (e.g. French) skills are desirable Passion for healthcare products and the underlying technical and regulatory compliance aspect Developing leadership skills with evidence in effective negotiation, strategic thinking and prioritisation #LI-WP1 We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally. Find out more about Total Rewards at Perrigo. We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more here Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. Our full Equal Employment Opportunity and Affirmative Action Policy Statement is available on our main career site in English and Spanish and will be provided in other accessible forms for persons with disabilities. #DIV