Ra-Cmc Specialist

hace 1 mes


Barcelona, España Galderma A tiempo completo

With a unique legacy in dermatology as well as decades of cutting-edge innovation, Galderma is the pure-play dermatology category leader, present in approximately 90 countries. We deliver an innovative, science-based portfolio of premium flagship brands and services that spans the full spectrum of the fast-growing dermatology market through Injectable Aesthetics, Dermo-cosmetics, and Therapeutic Dermatology. Since our foundation in 1981, we have dedicated our focus and passion to the human body's largest organ – the skin – meeting individual consumer and patient needs with superior outcomes in partnership with healthcare professionals. We look for people who focus on getting results, embrace learning and bring a positive energy. They must combine initiative with a sense of teamwork and collaboration. Above all, they must be passionate about doing something meaningful for consumers, patients, and the healthcare professionals we serve every day. Job Title: Regulatory Affairs CMC Specialist Location: Barcelona Job Description We are looking for an expert in Regulatory Affairs for preparing and updating the CMC (Chemistry, Manufacturing and Control) dossier sections of assigned products (Rx or non-monograph OTC drugs). This person will contribute to develop RA-CMC strategies for geographical extension and for post-approval CMC activities. Key Responsibilities Contribute to global regulatory CMC strategies.Assess regulatory impact of proposed CMC changes and contribute to the CMC regulatory strategies that support change implementation.Review data provided to support dossier preparation; identify gaps and risks and work with stakeholders to solve them.Write/assemble CMC sections of regulatory submissions.Develop and maintain project plans and schedules for CMC submissions.Ensure all CMC dossiers are stored in the company database.Provide guidance minimally on ICH, FDA and EU CMC guidelines.Develop and maintain excellent relationships with internal functional groups, contract manufacturing organizations and other relevant partners to ensure alignment of regulatory CMC strategies and successfully accomplish regulatory goals.Share knowledge and experience with other team members.Collaborate with service providers contracted to support a project, if appropriate. Skills & Qualifications Effective experience in CMC Regulatory Affairs.Background in pharmaceutical industry.Experience with topical and/or systemic drugs (Biologics and/or Small Molecules). What we offer in return You will be working for an organization that embraces diversity & inclusion and believes we will deliver better outcomes by reflecting the perspectives of our diverse customer base.You will receive a competitive compensation package with bonus structure and extended benefit package.You will be able to work in a hybrid work culture.You will participate in feedback Loops, during which a personalized career path will be established.You will be joining a growing company that believes in ownership from day one where everyone is empowered to grow and to take on accountability. Process steps Send your CV in English.If your profile is a match, we will invite you for a first virtual conversation with Talent Acquisition.The next step is a virtual conversation with the hiring manager.The final step is a panel conversation with the extended team. Our people make a differenceAt Galderma, you'll work with people who are like you. And people that are different. We value what every member of our team brings. Professionalism, collaboration, and a friendly, supportive ethos is the perfect environment for people to thrive and excel in what they do.
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