As the Regulatory Innovation Senior Scientist, your job purpose is to:
- Play a critical role in driving Alliance's innovation agenda by providing strategic regulatory expertise across our diverse product portfolio - including medical devices, cosmetics, food supplements, and medicines.
- Ensure global regulatory compliance while enabling the successful development, approval, and commercialization of innovative products that support long-term business growth.
What you'll be doing:
- Represent the regulatory function, develop and implement optimal regulatory strategies to ensure compliance and commercial success.
- Lead the development of regulatory strategies for innovation opportunities to ensure successful launch of new products.
- Responsible for departmental QMS activities, ensuring compliance with standards and regulations.
- Engage in continued training and professional development activities to achieve team goals and objectives.
- Represent the EMEA regulatory advisory opinion at innovation meetings and provide input to meet corporate needs.
- Provide technical expertise and advisory support to the business on regulatory matters, specifically related to innovation.
- Support the team to ensure strategic business objectives are met according to prioritized goals and projects.
- Collaborate with cross-functional teams, including R&D, marketing, quality, and commercial functions, to embed regulatory considerations early in product development.
- Engage with regulatory subject matter experts, authorities, and external partners to support regulatory strategy and pathways for innovative products.
- Identify and mitigate regulatory risks associated with novel product development and innovation initiatives.
Qualifications:
- A bachelor's degree or equivalent in a life or physical science, engineering, or similar related field.
- Extensive experience in Regulatory Affairs within the consumer healthcare industry.
- Proven track record of successfully delivering global regulatory approvals and related authorizations, including UK and EU.
- Strong project management skills, including planning, scheduling, and risk management.
- Familiarity with all regulatory application processes for healthcare products, particularly medical devices.
- Familiarity with electronic and physical product information repositories, including databases and file submissions, for effective management of product approvals.
- Excellent communication, presentation, and stakeholder management skills.
- Strategic thinking with a hands-on approach to application management.
- Comfortable working in a regulated global environment.
- Strong interpersonal skills and the ability to influence without authority, manage conflict, and foster alignment across diverse teams.
Join us:
Are you ready to be part of something extraordinary? At Alliance, we're a dynamic, science-led consumer healthcare organization specializing in advanced skincare solutions and vitamins, minerals & supplements (VMS). Backed by innovation and driven by purpose, we're on an exciting journey of transformation and growth—expanding our reach, enhancing our brands, and bringing cutting-edge products to more consumers worldwide.
As we evolve, we're seeking passionate, curious, and driven individuals to join us. If you're excited to shape the future of health and wellness in a fast-paced, entrepreneurial environment—this is your moment. At Alliance, you'll be part of a purpose-driven business that empowers people. We offer a supportive, collaborative culture with real opportunities to grow your career as we grow our brands. If you want to make a difference and be part of something exciting, we'd love to hear from you.