Senior Regulatory Affairs CMC Professional
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Søborg
Do you have experience from either RA, CMC, QA, and/or QC – or any other relevant area? Do you possess a natural interest and flair for regulatory guidelines? Do you enjoy being part of a team where you together build and work on the timely delivery of successful submissions? Then you might be one of the people we are looking for. Regulatory Affairs CMC & Device (RA CMC & Device) is on a fortunate journey with our organization growing and expanding because of a developing and flourishing product portfolio. We are therefore seeking several RA CMC professionals to support the RA CMC work across different stages of projects in different indications. Apply now for a life-changing career! The Position As a Regulatory Affairs CMC professional, you provide the key connection between scientists and regulators to make medicines available to patients around the world by ensuring fast and successful regulatory submissions and approvals in all global markets. Your responsibilities will include: You will join an organization where there are opportunities to work across the various phases of clinical development, including early and late-phase clinical studies, planning, and executing meetings with the health authorities, and QnAs, and submitting marketing authorization applications. Operating as a senior RA CMC professional you will be in the center of project planning and execution – responsible for participating in establishing realistic – and at times bold – RA strategies. You will Together with the project team, you will be planning and due diligently to ensure timelines are met. A cornerstone in the RA CMC operation is the coordination and review of regulatory documentation packages, including also supporting the preparation of applicable sections of submission packages, responses to agency questions, and agency meeting packages. You will be part of an RA CMC project team and a project core team. In the project team, you will be responsible for giving input from the RA CMC perspective and participating in establishing submission timelines and support decisions on the extent of data needed for a filing to receive HA approval. Additional aspects of the role include identifying as well as improving regulatory CMC practices, processes, and approaches related to regulatory CMC documentation and strategies. Qualifications You come with a scientific background and mindset, which you have acquired through your extensive experience in pharmaceutical operations – manufacturing, product supply, process development, CMC development, analytics, quality assurance, and other related areas. The ideal candidate should have: Master's degree and/or PhD in a relevant field At least 5 years of relevant experience within the pharmaceutical industry High proficiency in English - written as well as spoken Great communication skills as all work takes place in multidisciplinary project groups A pro-active, positive, and friendly professional style Enjoy being part of teams with people from diverse backgrounds You are a dedicated team player, you find it easy to build working relationships and gain recognition amongst stakeholders with your proactiveness and integrity. Furthermore, you thrive in the challenging reality of international communication across time zones and cultures. About the Area and Department RA CMC & Device consists of six areas with three working specifically with RA CMC functionality. We are skilled, collaborative, friendly, and dedicated colleagues with diverse backgrounds and experience, and you will be part of a dynamic and committed organization handling many projects in different phases of development. Also, as ’s product portfolio grows, RA CMC & Device is also looking into developing innovative solutions to increasingly complex CMC manufacturing strategies and regulatory requirements. There is a high focus on individualized onboarding, flexibility, empowerment, and individual development in the area. Well-being and psychological safety are also a major focus and are considered essential for the working environment. We strive for a modern way of working, including friendly colleagues, camaraderie, and space to be proactive, to learn, and to take the initiative to improve and make a difference. We want it to be the best place to work – not only in words, but we walk the talk in this area. Our commitment to innovation also applies to the way we work. We therefore embrace the hybrid workplace – with a blend of home office and on-site work. Visit our Regulatory Affairs Careers webpages For more information about job content and qualifications, please visit the Regulatory Affairs Careers webpages at Contact For more information regarding the role, you are welcome to contact Michala Ebba Victor on + Deadline 19 May 2024 If you are interested in this role, please apply as soon as possible. Applications will be evaluated on an ongoing basis. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At , we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds, and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve, and communities we operate in. Together, we’re life changing. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 2.5.2024, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Apoteker
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