What are the responsibilities and job description for the Quality Control Analyst II position at myGwork - LGBTQ Business Community?
This job is with Reckitt, an inclusive employer and a member of myGwork – the largest global platform for the LGBTQ business community. Please do not contact the recruiter directly. 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. 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 Step into a dynamic role where your expertise with ICP‑MS instrumentation drives the quality and safety of products reaching customers around the world. As a Quality Control Analyst II, you'll lead advanced elemental analysis, troubleshoot complex analytical challenges, and help shape continuous improvement initiatives in a fast‑paced lab environment. You'll collaborate with a passionate scientific team to ensure every result meets the highest regulatory and technical standards. If you're energized by precision, innovation, and hands‑on analytical work, this is the opportunity to elevate your impact.Your responsibilities
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 Step into a dynamic role where your expertise with ICP‑MS instrumentation drives the quality and safety of products reaching customers around the world. As a Quality Control Analyst II, you'll lead advanced elemental analysis, troubleshoot complex analytical challenges, and help shape continuous improvement initiatives in a fast‑paced lab environment. You'll collaborate with a passionate scientific team to ensure every result meets the highest regulatory and technical standards. If you're energized by precision, innovation, and hands‑on analytical work, this is the opportunity to elevate your impact.Your responsibilities
- Operate, maintain, and troubleshoot ICP‑MS instrumentation to ensure accurate and reliable analytical results.
- Perform testing and analysis of raw materials, in‑process samples, and finished products using validated ICP‑MS methods.
- Analyze and document ICP‑MS test data, generating clear and compliant quality reports.
- Support investigations of out‑of‑specification (OOS) or out‑of‑trend (OOT) results related to ICP‑MS testing, contributing to root‑cause analysis.
- Participate in method transfers, validation, and continuous improvement initiatives involving ICP‑MS workflows.
- Bachelor's degree in Chemistry, Biochemistry, Biology, or a related scientific field.
- Minimum of 2 years of quality control or quality assurance experience in a regulated environment.
- Experience performing laboratory testing on raw materials, in‑process samples, and finished products, as well as operating and troubleshooting ICP‑MS instrumentation.
- Experience analyzing test data, preparing quality documentation or reports, and supporting OOS/OOT investigations.
- Experience with method transfers, method validation, and laboratory process improvements.
- VISA sponsorship, international movement and relocation assistance will not be offered for this role.