Micro Analyst

Reckitt•Wilson, NC

9d•Onsite

About The Position

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 roleThe QC Micro Analyst plays a vital role in safeguarding product quality through the hands‑on execution of microbiological testing and quality system support within the QC laboratory. Working under the guidance of the QC Microbiology Team Lead or QC Laboratory Manager, this role ensures laboratory operations are performed efficiently, accurately, and in full compliance with Good Laboratory and Documentation Practices. The position supports organizational quality and customer service goals by delivering reliable, timely laboratory results while demonstrating growing independence, strong attention to detail, and accountability for the integrity, accuracy, and quality of all work performed.

Requirements

Hands‑on microbiological laboratory experience (minimum 1 year full‑time preferred), ideally within a regulated manufacturing environment such as food, dietary supplements, or pharmaceuticals.
Practical experience performing microbiological testing using USP and BAM methods, including bioburden testing, pathogen screening, and environmental and water monitoring.
Working knowledge of GMP and GLP requirements, with demonstrated experience generating accurate, compliant laboratory documentation.
Proven ability to work independently while exercising sound judgment, delivering reliable results, and collaborating effectively with cross‑functional teams.
Experience using laboratory data management systems (e.g., LIMS) and strong working proficiency in Microsoft Word, Excel, PowerPoint, and Outlook for documentation and reporting.

Nice To Haves

Commercial Awareness
Business Partnership
Collaboration
Partnership building
Ability to challenge the status quo
Propose improvement
Accountability
Adaptability
Collaborator
R&D
Product Lifecycle Management

Responsibilities

Perform microbiological and analytical testing, including water and environmental monitoring, in compliance with cGMP, GLP, and GDP requirements.
Review, document, and maintain accurate microbiological data and records to ensure data integrity, traceability, and inspection readiness.
Ensure laboratory equipment is properly maintained, calibrated, and operated according to approved procedures, while upholding high standards of housekeeping and organization.
Support quality systems activities such as OOS, deviations, investigations, change controls, CAPA, and audit preparation, including participation in internal, external, and regulatory inspections.
Effectively manage daily workload, communicate issues and improvement opportunities, support team and line management objectives, and drive continuous improvement through professional development.