Overview
Continuous Improvement Manager (Wilson, NC, US, 27893)
We are Reckitt
Supply
About the role
The RPS Manager is responsible for driving a culture of continuous improvement and operational discipline across manufacturing site producing oral solid dosage and liquid products. This role leads the deployment of Lean, Six Sigma, and structured problem-solving methodologies while ensuring full compliance with cGMP, regulatory, and quality standards.
This role establishes foundational performance management systems, standard ways of working, and continuous improvement capability. The position plays a critical role in supporting facility start-up, process qualification, regulatory readiness, and rapid scale-up to commercial operations. The role partners closely with Manufacturing, Quality, Engineering, Planning & Logistics, and EHS.
Your responsibilities
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Deploy site Operational Excellence strategy aligned with RPS and MOS; standardize processes, metrics, and ways of working across all functions.
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Lead performance management systems including tiered meetings, KPI reviews, and visual management.
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Drive Lean initiatives (VSM, 5S, Kaizen, standard work, waste elimination) and apply Six Sigma tools (DMAIC, SPC, RCA) to resolve complex issues and embed sustainable, cGMP‑compliant improvements.
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Ensure OpEx activities meet cGMP, data integrity, and quality system requirements; partner with Quality to maintain compliance; support inspections and audits; follow change control and risk/validation processes.
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Improve RFT, cycle time, throughput, OEE, asset utilization, deviations, CAPA effectiveness, inventory, and material flow; support OSD and liquid dosage manufacturing operations.
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Build site OpEx capability through training, coaching, and mentoring; develop Lean leaders and Belts; drive a continuous improvement culture and mindset shift.
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Use data and analytics to identify gaps and prioritize improvements; partner with IT and operations to leverage digital tools (MES, EBR, CMMS, dashboards) and enhance data accuracy and visibility.
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Lead cross‑functional improvement projects; run governance forums to track initiatives, benefits, and risks; communicate progress to site and global leadership.
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Quantify, validate, and sustain OpEx financial benefits (cost, productivity, capacity); support annual plans and long‑range strategy.
This role is not currently sponsoring visas or considering international movement at this time.
The experience we're looking for
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Bachelor’s degree in Engineering, Science, Pharmacy, or related field; 7–10 years in pharmaceutical or regulated manufacturing and 3–5 years in Operational Excellence, Lean, or Continuous Improvement.
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Production line or facilities experience in vitamin, food, chemical, or pharmaceutical environments, with a proven track record of improving processes and systems.
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Strong analytical skills and a demonstrated drive to implement improvements; Lean Six Sigma Green Belt or Black Belt.
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Experience with site startup, tech transfer, or scale‑up; familiarity with MES, LIMS, SAP, and CMMS systems.
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Project Management (PMP or equivalent) and/or Change Management training or certification.
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Strong understanding of cGMP and pharmaceutical quality systems, with practical application of Lean, Six Sigma, and structured problem‑solving.
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Knowledge of OSD and/or oral liquid manufacturing processes and experience working within change control, deviation, CAPA, and validation systems.
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Ability to work effectively with incomplete data and in evolving, fast‑changing processes.
The skills for success
What we offer
Salary Range
USD $140,000.00 – $210,000.00
Hiring range up to 170K
Pay Transparency
Equality
IMPORTANT: Before applying for this role, please make sure you have the right to work in the country where the role is based. Unless it clearly stipulates within in the job advert above that the hiring company is looking to or able to sponsor applicants it is deemed that the hiring employer will only consider applications from those able to comply with and work in the country where the role is based.













