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Novartis

Process Team Lead

İstanbul Kurtköy

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hirly's read of this role

Seniority
Lead / management
Country
TR
Work mode
On-site / unstated
First seen by hirly
3 Oct 2026

Derived automatically from the posting. Upload your resume above to see how the role scores against it.

the posting

Band

Level 4

Job Description Summary

  • Job Purpose
  • The Process Team Lead is responsible for overseeing daily manufacturing operations within the Manufacturing Unit, fostering a culture of empowerment, accountability, and continuous improvement. The role ensures the delivery of high-quality products in compliance with GMP, HSE, and Novartis standards while maximizing operational efficiency, productivity, and team performance.

Job Description

Major Accountabilities

Manufacturing Operations & Shop Floor Leadership

  • Provide visible leadership on the shop floor through regular presence, walkthroughs, and operational support.
  • Ensure adequate resource planning and allocation based on production workload and business priorities.
  • Review and manage production schedules within the operational horizon, considering risks, constraints, and opportunities.
  • Ensure continuity of production flow through effective coordination of personnel, materials, consumables, equipment, documentation, and supporting services.
  • Set operational priorities and adjust plans when unforeseen events occur.
  • Optimize the utilization of human and technical resources to meet safety, quality, delivery, and cost objectives.
  • Monitor and drive implementation of CAPAs and actions related to operational performance indicators.
  • Own shop floor service support activities and management of external workforce supporting cleaning and material handling operations.
  • Support technical batch release activities, including batch record review, SOP maintenance, and process documentation management.
  • Lead incident reporting, investigations, root cause analyses, and implementation of corrective and preventive actions.
  • Demonstrate ownership of manufacturing processes and products, ensuring sustainable operational performance.

Leadership & People Development

  • Act as a role model for Novartis Values & Behaviors and promote a culture of trust, collaboration, accountability, and inclusion.
  • Translate strategic objectives into clear team goals, priorities, and action plans.
  • Build, engage, and motivate high-performing teams that consistently deliver business results.
  • Ensure associates are appropriately trained and qualified before performing GMP activities independently.
  • Monitor training compliance and competency development of team members.
  • Provide coaching, feedback, and performance management support to direct reports and Shift Leaders.
  • Facilitate effective decision-making and problem-solving within the team.
  • Promote cross-functional collaboration and knowledge sharing across manufacturing teams.
  • Support talent development, succession planning, and employee engagement initiatives.

Quality, Compliance & HSE

  • Ensure full compliance with GMP, HSE, Novartis Quality Management Systems, and applicable regulatory requirements.
  • Maintain inspection readiness and support successful internal and external audits and regulatory inspections.
  • Promote a strong safety and quality culture through leadership, accountability, and continuous awareness.
  • Ensure implementation and effectiveness of Business Continuity Plans within the area of responsibility.
  • Act as the owner of quality and compliance practices defined within the Novartis Manufacturing Manual.
  • Drive proactive identification, reporting, and resolution of quality and safety risks.

Continuous Improvement & Operational Excellence

  • Champion Operational Excellence through Lean Leadership, Visual Management, Tiered Accountability, Leader Standard Work, and Gemba practices.
  • Lead improvement initiatives including TPM, process optimization, technology transfer, digitalization, and productivity improvement projects.
  • Drive improvements in Overall Asset Effectiveness (OAE), yield, cycle time, and operational performance metrics.
  • Facilitate Root Cause Investigations (RCIs), Kaizens, and problem-solving workshops to eliminate losses and improve performance.
  • Utilize data analytics, visualization, and performance monitoring to identify improvement opportunities.
  • Ensure sustainability of implemented improvements and achievement of targeted business benefits.
  • Contribute actively to site Continuous Improvement strategy and project prioritization activities.

Key Performance Indicators

People

  • Employee engagement and satisfaction
  • Training compliance and qualification status
  • Talent development and succession readiness
  • Retention and attraction of key talent

Supply & Delivery

  • Production volume achievement
  • Schedule adherence
  • Launch and commercialization performance
  • Supply Excellence KPIs

Quality & Compliance

  • Batch success rate
  • Right-First-Time performance
  • Audit and inspection outcomes
  • Reduction of human error-related deviations
  • Batch documentation quality

Safety

  • Lost Time Injury (LTI) rate
  • Safety observation and action completion performance

Cost & Productivity

  • Budget adherence
  • Headcount management
  • Cost of non-quality reduction
  • Yield and OAE improvements

Continuous Improvement

  • Delivery of Operational Excellence projects
  • Financial benefits generated through improvement initiatives
  • Sustainability of implemented actions

Essential Requirements

Education

Bachelor's Degree in Pharmacy, Chemical Engineering, Chemistry, Pharmaceutical Technology, Life Sciences, or a related field.

Experience

  • Minimum 5 years of experience in the pharmaceutical or life sciences industry within a GMP-regulated environment.
  • Minimum 2 years of people leadership or supervisory experience is preferred.
  • Experience in commercial manufacturing operations is highly desirable.

Technical & Functional Skills

  • Strong knowledge of GMP regulations and pharmaceutical manufacturing processes.
  • Good understanding of Quality Systems and Health Authority requirements.
  • Experience with manufacturing systems (MES, SAP, or equivalent).
  • Knowledge of Lean Management and Operational Excellence methodologies.
  • Experience in process improvement, problem solving, and root cause investigation.

Leadership Competencies

  • Strong leadership and people development capabilities.
  • Effective communication, influencing, and stakeholder management skills.
  • Proven ability to lead change and drive organizational performance.
  • Strong analytical and problem-solving mindset.
  • Ability to work effectively under pressure in a fast-paced manufacturing environment.

Languages

  • Advanced English proficiency.
  • Fluent Turkish.

Skills Desired

Data Analytics

Original posting on Novartis's site ↗

Listed on hirly, a job board. hirly is not the employer: Novartis is hiring for this role.

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