Area Quality Leader
We are Reckitt
Research & Development
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
As an Area Quality Leader at Reckitt, you play a critical role in safeguarding the integrity of some of the world’s most trusted health brands. You are the champion of quality on the manufacturing floor—driving compliance, elevating performance, and ensuring every product leaving our Wilson facility meets the highest standards of safety, reliability, and consumer confidence.
In this role, you oversee day‑to‑day Quality System operations across the entire site, spanning warehouse, incoming goods, manufacturing, packaging, and laboratory environments. You shape and execute quality improvement initiatives, embed robust quality systems, and ensure operational teams are fully aligned with regulatory expectations and best practices.
You serve as a hands‑on partner to both Quality and Operations teams, providing real‑time feedback, guiding performance against quality requirements, and leading the remediation of issues through proactive and corrective actions. Your leadership helps prevent problems before they arise—and ensures swift, effective response when they do.
Your responsibilities
- Oversee day-to-day Quality System activities across warehouse, incoming goods, manufacturing, packaging, and laboratory areas to ensure compliance with regulatory and internal standards.
- Lead the planning, implementation, and embedding of quality improvement initiatives and system enhancements across the Wilson facility.
- Partner closely with Quality and Operations teams to monitor performance against quality requirements and provide timely, actionable feedback.
- Guide the remediation of quality issues by driving proactive and reactive CAPA activities that address root causes and strengthen operational reliability.
- Support continuous compliance by maintaining robust quality processes, fostering cross-functional alignment, and ensuring quality expectations are met throughout the product lifecycle.
This role is not currently sponsoring visas or considering international movement at this time.
The experience we're looking for
- Bachelor’s degree in a scientific or technical discipline (e.g., Chemistry, Chemical Engineering, Industrial Engineering, Mechanical Engineering, Manufacturing Engineering).
- 3–5 years of experience in quality assurance within the pharmaceutical or medical device industry, including work with oral solid dosage manufacturing processes.
- Direct experience applying quality management systems, Title 21 CFR requirements, and industry best practices in a regulated manufacturing environment.
- Hands‑on experience supporting regulatory audits and working with governmental agencies, external partners, and internal cross‑functional teams.
- Practical experience using electronic quality management systems and industry‑standard quality tools such as SPC, Advanced Quality Planning, Control Plans, FMEA, root‑cause analysis, Six Sigma methodologies, and cross‑functional problem‑solving approaches.
The skills for success
Commercial Awareness, Business Partnership, Collaboration, Partnership Building, Ability to Challenge the Status Quo, Propose Improvements, Accountability, Adaptability, Collaborator, R&D, Product Lifecycle Management.
What we offer
US salary ranges
USD $85,000.00 - $127,000.00
Hiring range up to $105K
US pay transparency
Equality
Nearest Major Market: Raleigh
Nearest Secondary Market: Rocky Mount
Job Segment:
Medical Device, Nutrition, Counseling, Healthcare