Senior Regulatory Affairs Manager

Regional Regulatory Strategy ManagerSupport the Senior Director in developing and executing regional regulatory strategies for quality-of-life initiatives within specific regions.Contribute to providing strategic oversight and leadership to the regulatory team, ensuring alignment with company objectives and regional regulatory requirements.Participate in the preparation and submission of regulatory documents related to quality-of-life initiatives to regulatory authorities.Collaborate with cross-functional teams to integrate quality-of-life considerations into product development, manufacturing, and commercialization processes.Assist in fostering relationships with regional regulatory authorities to facilitate communication, negotiations, and interactions related to quality-of-life initiatives.Stay informed about regulatory developments, changes, and trends within specific regions, and provide insights to the Senior Director and Associate Director.Contribute to managing regulatory risks and opportunities related to quality-of-life initiatives and assist in developing mitigation strategies as needed.Provide regulatory guidance and support for post-marketing activities related to quality-of-life initiatives, including variations, renewals, labeling updates, and compliance initiatives.Collaborate with the regulatory team to represent the company's interests in industry forums, working groups, and regulatory meetings related to quality-of-life initiatives.Support coordination with global regulatory counterparts to ensure alignment of regional regulatory strategies and submissions with global development plans and corporate objectives.Assist in preparing regulatory updates, progress reports, and strategic recommendations for senior and/or executive leadership and regulatory governance committees.Assists in preparing and organizing all necessary documentation required for regulatory inspections and inspection readiness initiatives ensuring completeness, accuracy, and accessibility of records related to quality-of-life initiatives.Participates in facilitating communication, providing requested documentation, and addressing any questions or concerns raised by the inspection readiness team in a timely and professional manner.Bachelor's degree in a scientific discipline such as life sciences, pharmacy, bioscience; advanced degree preferred.5+ years of experience in regulatory affairs within the pharmaceutical or biotech industry, with a focus on quality-of-life products preferred.Must have branded product reg affairs experience.Demonstrated ability to work effectively in a cross-functional team environment.Strong knowledge of regional regulatory requirements and guidelines, including FDA regulations and ICH guidelines.Excellent communication and interpersonal skills.Ability to assist in developing and executing regulatory strategies tailored to specific regions.Strong organizational skills with attention to detail.Ability to collaborate effectively with cross-functional teams.Knowledge of regulatory submissions and documentation processes.Awareness of regulatory developments and trends within specific regions.Strong analytical and problem-solving skills.Ability to work independently and prioritize tasks effectively.Ability and willingness to travel approximately 10% of the year both domestically and internationally.