Product Development à United States

In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.

We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.

The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.

This role is integrated within the Medical Sciences team, responsible for medical science and evidence generation activities during the development and throughout the entire life cycle of RB Hygiene products. The role works with Medical Science Managers and brand team to drive commercial success by generating and applying medical insights to deliver high quality evidence that results in safe, efficacious and meaningful innovation to consumers.

Hiring Manager - Fiona Burke,

Independently represent the Medical Sciences team and contribute expertise in cross-functional project meetings.

• Conduct a fair-balanced assessment of efficacy and safety data and provide advice on the best approach to drive brand growth through product development and roll out.
• Provide input and review to Regulatory and Clinical Documents required for global product development and registration activities. These include but are not limited to: briefing documents, common technical document (CTD) clinical overviews and summaries, switch applications, integrated summaries of safety and efficacy, investigators' brochures, clinical documents such as Study Protocols and Informed Consent Forms; clinical evaluation reports (CERs) and other Medical/Regulatory documents.
• Manage internal and external responses, and ensure quality of medical documentation for given area/projects.
• Collaborate with subject matter experts across multiple departments to ensure quality and technical accuracy of documentation.
• Conduct systematic literature searches/reviews and prepare responses as necessary.
• Edit and proofread text written by other team members and provide constructive feedback.
• Ensure that working documents and other appropriate documentation are updated and current.

Qualifications and experience:

• Bachelor's Degree preferably related to healthcare or life sciences (e.g., basic science, pharmacy, nursing, or medical).
• Experience in the medical and pharmaceutical / consumer health industry is required.
• Experience in health care product development and medical writing is highly desirable.
• Knowledge of research methodology, regulatory requirements, and healthcare compliance is desirable.
• Proven ability to analyze and interpret scientific and clinical data.
• Experience of product development, clinical development, or successful product launches.
• Ability to manage multiple projects effectively.
• Strong communication skills and ability to work in a fast-paced environment.

Skills for success include: task execution under pressure, business acumen, commercial awareness, strategic planning, accountability, consumer insight, collaboration, innovation, and adaptability.

Join us in our mission to protect, heal, and nurture in the relentless pursuit of a cleaner, healthier world. Be part of a global team committed to making access to high-quality hygiene, wellness, and nourishment a right, not a privilege.