Manager Operational Excellence - On Site

Manager Operational Excellence - On Site

Job Category
:
Production

Requisition Number
: MANAG
005795

• Posted :
  May 20, 2026
• Full-Time
• On-site

Windsor CO Windsor, CO 80550, USA

The Manager Operational Excellence is a member of the Corporate Operational Excellence organization and provides leadership for implementing and sustaining a continuous improvement culture across cGMP-regulated pharmaceutical manufacturing operations. This role drives operational excellence in a manner that strengthens quality systems, improves process capability and reliability, supports inspection readiness, and advances patient safety, supply continuity, and cost performance.

The OpEx Manager partners with the VP Business Strategy/CI and site leadership to lead cultural change using Lean and Six Sigma tools within a regulated manufacturing environment. This role also provides direct leadership to the Operational Excellence team, including setting priorities, developing capability, and ensuring resources are aligned to the highest-value initiatives. The role works cross-functionally with Manufacturing, Quality Assurance, Quality Control, Engineering, Validation, Supply Chain, and Regulatory teams to simplify processes, reduce waste and variation, improve right-first-time performance, shorten cycle times, strengthen batch release performance, and embed the Tolmar Operating System throughout the organization.

• Lead and facilitate operational excellence initiatives across pharmaceutical manufacturing and support functions, ensuring alignment with cGMP requirements, quality standards, and business priorities.
• Directly supervise the Operational Excellence team, including hiring, onboarding, coaching, performance management, development planning, succession planning, and day‑to‑day prioritization of resources and deliverables.
• Identify and prioritize improvement opportunities that enhance safety, quality, delivery, inventory, and cost performance while maintaining validated state and compliance.
• Partner with Manufacturing, Quality, Engineering, Validation, Supply Chain, and other functions to improve process flow, equipment utilization, capacity, and schedule adherence.
• Support site and functional diagnostics to assess current‑state performance; establish data collection methods, KPIs, and visual management systems to monitor progress and sustain gains.
• Facilitate Kaizen events, value stream mapping, Gemba walks, and root cause problem‑solving workshops focused on reducing deviations, rework, scrap, downtime, and cycle time.
• Assist in the development and execution of tactical improvement plans, including resource needs, timelines, risk mitigation, and change management actions.
• Apply and promote continuous improvement tools and systems, including 5S, visual management, standard work, DMAIC, control plans, mistake proofing, 5 Whys, and CAPA‑related root cause analysis.
• Track the performance and maturity of improvement initiatives and report progress to site and business leaders, with emphasis on compliance, throughput, yield, batch release, and service‑level outcomes.
• Support inspection readiness by improving process discipline, documentation practices, training effectiveness, and adherence to standard operating procedures.
• Lead the Operational Excellence team through regular goal setting, performance reviews, coaching, workload balancing, and professional development to build sustainable site capability in Lean, Six Sigma, and structured problem solving.
• Perform other related duties as assigned.

• Strong knowledge of current Good Manufacturing Practices (cGMP), FDA expectations, and applicable international regulations for pharmaceutical manufacturing.
• Working knowledge of pharmaceutical quality systems, including deviations, CAPA, change control, document control, training, and inspection readiness.
• Experience using data collection, statistical analysis, and performance management tools to improve process capability, reduce variability, and drive fact‑based decisions.
• Experience operating in a Lean culture within a regulated manufacturing environment.
• Ability to work effectively in a team‑based culture…