R&D PDM Assistant

We are Reckitt

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.

The team

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.

About the role

We are seeking a detail-oriented individual to join our team as an R&D PDM Assistant with a minimum of 1-2 years’ experience in an analytical testing laboratory or a manufacturing facility. This individual will be integral in the start-up and technology transfer for our R&D laboratory, supporting the launch of a new GMP manufacturing production site for Over-the-Counter (OTC) products and Vitamins, Minerals, and Supplements (VMS), based in Wilson, North Carolina. 

Your responsibilities

The R&D PDM Assistant is responsible for:

• Supporting technology transfer of processes and equipment to the Wilson site from other Reckitt sites.
• Supporting trials for novel technologies involved in the OTC and VMS manufacturing processes.
• Supporting analytical method transfer activities, including protocol execution and laboratory notebook second scientist review (SSR), for raw material, intermediate and finished product test methods
• Assist in method validation and USP verification studies in accordance with ICH and USP guidelines
• Conduct USP compendial testing (e.g., assay, dissolution, content uniformity, identification, etc.)
• Maintain accurate and complete laboratory records in compliance with GMP and GLP standards
• Prepare and review technical documentation including equipment qualification protocols and reports, standard operating procedures (SOPs) etc.