Quality Control Analyst/Associate (II)- Second Shift

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.

​Research & Development​

In R&D, 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 R&D Academy, designed to develop our team and allow you to grow in our great organisation.

About the role

We are looking for a Second Shift (Monday through Friday, ideally 4:00 PM-Midnight) Quality Control Analyst II to support our commitment to product quality and regulatory compliance. In this role, you will perform laboratory testing on raw materials, in-process samples, and finished products to ensure they meet company specifications and regulatory standards. You will also analyze test results, conduct peer reviews, and contribute to continuous improvement initiatives. This position requires expertise in analytical techniques, method validation, troubleshooting, and GMP compliance to maintain the highest quality

Your responsibilities

• Perform testing and analysis on raw materials, in-process products, and finished goods using validated methods.
• Operate, maintain, and troubleshoot HPLC and GC instruments to ensure accurate and reliable results.
• Analyze test data, document findings, and generate detailed quality reports.                              
• Support investigations of out-of-specification (OOS) and out-of-trend (OOT) results and contribute to root cause analysis.
• Identify and resolve quality issues, working with cross-functional teams to implement corrective actions.
• Ensure compliance with GMP, FDA, and regulatory standards by following SOPs and QC procedures.
• Participate in method transfers, method validation, and process improvements to enhance QC efficiency.
• Train and mentor new analysts on QC procedures, equipment operation, and data analysis.

The experience we're looking for

• Bachelor’s degree in Chemistry, Biochemistry, Biology, or a related scientific field.
• 2+ years of experience in quality control or quality assurance in a regulated environment.
• Hands-on experience with HPLC and GC is required.
• Familiarity with analytical techniques, method validation, and troubleshooting.
• Knowledge of regulatory requirements such as GMP, FDA, EP, and USP guidelines.
• Strong attention to detail, problem-solving, and critical-thinking skills.
• Excellent communication skills and ability to work both independently and as part of a team.
• Ability to thrive in a fast-paced, deadline-driven environment while maintaining accuracy and compliance.
• Availability to work Second Shift (Monday through Friday, ideally 4:00 PM-Midnight)
• This role is not currently sponsoring visas or considering international movement at this time.

This role is ideal for an experienced QC professional seeking to apply their analytical expertise and regulatory knowledge to enhance product quality and compliance. If you meet the qualifications and are passionate about quality assurance, we encourage you to apply!

The skills for success

• Bachelor’s degree in Chemistry, Biochemistry, Biology, or a related scientific field.
• 2+ years of experience in quality control or quality assurance in a regulated environment.
• Hands-on experience with HPLC and GC is required.
• Familiarity with analytical techniques, method validation, and troubleshooting.
• Knowledge of regulatory requirements such as GMP, FDA, EP, and USP guidelines.
• Strong attention to detail, problem-solving, and critical-thinking skills.
• Excellent communication skills and ability to work both independently and as part of a team.
• Ability to thrive in a fast-paced, deadline-driven environment while maintaining accur