Job Description

Select how often (in days) to receive an alert: Regulatory Affairs Project Manager Woman's Health & Lifestyle Location: Ghent, BE, 9050 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 win in self-care. Description Overview Are you an experienced Regulatory Affairs Project Manager with business acumen and a keen eye for detail? We are looking for a new colleague to reinforce the regulatory activity required to submit, approve and launch new products and the maintenance of existing commercialized products and dossiers. In this role, you will be a key advisor to internal teams and external stakeholders, contributing to successful product registrations and market access. Scope of the Role Assist in execution of regulatory activities per the project plan to assure new products meet submission, approval and commercial launch goals Highly involved in the products lifecycle, including New Product Development (NPD) and launches, lifecycle maintenance and promotional activities Support manufacturing and procurement in the management of change to existing commercial products Maintain product labeling in compliance with local and EU laws and regulations; develop and approve label specifications in compliance with SOPs Support the development and approval of packaging materials in a timely manner Process change requests in compliance with GMPs and regulations Maintain regulatory files and data systems in compliance with SOPs Ensure timely and effective communication and collaboration with other departments including marketing, CS&I (trade marketing), sales and corporate regulatory and innovation Review technical documentation and manage regulatory submissions in a timely manner Process feedback from regulatory authorities and notified bodies Support the development and clearance of promotional materials Provide input for analysis of data and/or management review, if required Assist in the process of reporting and investigating critical non-conformities and opportunities for improvement Experience Required Masters degree in Life Sciences, Pharmacy, or a related field; a pharmacist degree is an asset At least 4 years of experience in Regulatory Affairs In-depth knowledge of local and EU regulations; at least in one of the countries of BeNe Strong communication and project management skills Recognized as Person Responsible for Information & Publicity (RIP) in Belgium is a strong asset Background knowledge of other types of consumer healthcare products, food supplements or cosmetics is an asset The ability to work both autonomously and in teams Strong communication, persuasion and problem-solving skills An eager and quick learner Fluent in Dutch and English; knowledge of French and German is an asset Benefits 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. Hybrid Working Approach We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles. 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. #weareperrigo #J-18808-Ljbffr Perrigouk

Job Tags

Similar Jobs