Regulatory Senior Scientist in Chippenham

Reporting to the Global Regulatory Associate Director in Chippenham, Wiltshire - Hybrid (2 days onsite), we’re now looking for a Regulatory Senior Scientist to play a pivotal role within our Global Regulatory - Global Scientific Affairs & Innovation team.

The opportunity

• Lead the EMEA Medicines & RIMs Team and act as the primary regulatory lead for the medicine’s portfolio.
• Ensure the regulatory compliance and commercial success of our medicinal products, while also providing regulatory support to Medical Devices, Cosmetics and Food Supplements, as required.
• Oversee the management of all systems and data within the Regulatory Affairs function and involve strategic oversight, regulatory compliance, and cross-functional collaboration to drive global regulatory strategies.
• Foster a culture of global regulatory excellence and continuous improvement.

What you are responsible for

• Lead the management of the EMEA medicines portfolio and regulatory systems (RIMs), ensuring data integrity and compliance with applicable regulatory standards.
• Provide regulatory support to the medical devices, food supplements and cosmetics.
• Provide strategic direction and mentorship to Managers and Scientists (Medical, Quality and Regulatory) within the teams.
• Develop and implement optimal regulatory strategies to ensure compliance and commercial success.
• Provide regulatory strategy for innovation opportunities for successful launch of new products.
• Create, maintain and approve regulatory documentation, ensuring submissions to regulatory database, in accordance with relevant regulations.
• Manage departmental QMS activities, ensuring compliance with standards and regulations.
• Drive ongoing training and professional development activities to achieve team goals and objectives.
• Represent the EMEA regulatory advisory opinion at cross-functional meetings and provide strategic input to meet corporate needs.
• Provide technical expertise and advisory support to the business on regulatory matters.
• Optimise resource allocation to ensure our strategic business objectives are met according to prioritised goals and projects.
• Influence changes to the internal and external regulatory environment, contributing to stakeholder consultations and industry discussions.
• Represent the company in regulatory forums and advocate for best practices in regulatory affairs.

What we’re looking for

• Substantial experience in regulatory affairs within consumer healthcare, OTC, or FMCG.
• Proven experience working with Medicines and RIMs.
• Strong track record of authoring and submitting regulatory dossiers (NDA, ANDA, or equivalent) to bodies such as MHRA, EMA, or FDA.
• Deep understanding of complex product classifications across medicines, cosmetics, food supplements, and medical devices.
• Experience reviewing artwork, packaging, and promotional materials, ensuring compliance and scientifically supported claims.
• A confident leader with the ability to influence, mentor, and collaborate across global teams.

Why Alliance?

• High‑impact leadership role with genuine strategic influence.
• Collaborative, science‑led culture with global reach.
• Hybrid working to support flexibility and balance.
• Opportunity to shape regulatory excellence and innovation across multiple product categories.
• Great benefits include competitive salary, up to 25% bonus potential, up to 10% pension contribution, BUPA, Life Assurance, Cycle and Electric car schemes, etc.
• Work life balance - 25 days holiday, plus celebration and volunteering days, and option to buy an additional 10-day holiday.