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Bulk Shift Coordinator

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Onsite

Bulk Shift Coordinator

Grünenthal GmbH

Bulk Shift Coordinator

Skills

Compliance

2 months ago

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Important information


Location:

Quito, Ecuador

Work mode:

Onsite

Published on:

7 August 2026

What they need


​Management  |  Permanent  |  Full-time  |  On-Site​

Our people in Manufacturing & Global Operations share two priorities: getting things done and making things better. If you’re a dynamic person with a positive mindset, you’ll fit in well here. It’s an international team with a powerful spirit of collaboration. Together, we make sure our products meet the highest standards of quality by constantly searching for ways to improve at every stage of our value chain – from the raw materials we buy through to the logistics network that brings our medicines to patients. Join our team and help us make an even bigger contribution to Grünenthal’s future.

What the Role looks like

Every day, you will take on challenges that directly impact the quality of our products and the productivity of our plant, such as:

  • Coordinating and overseeing daily manufacturing operations, ensuring compliance with Environmental, Health, and Safety (EHS) standards, Good Manufacturing Practices (GMP), and productivity and service targets.
  • Ensuring that production processes are executed in accordance with approved procedures, while effectively managing the resources required to meet the manufacturing plan.
  • Managing deviations and operational events by driving containment actions, root cause analysis, and improvement plans to reduce risks and prevent recurrence.
  • Promoting workforce capability development, operational discipline, and continuous improvement through performance monitoring and systematic management of productivity losses, contributing to a safe, efficient, and compliant operation.

 

Your Contribution

To succeed in this role, we are looking for:

  • Degree in Pharmaceutical Chemistry or Pharmaceutical Biochemistry (mandatory).
  • Proven knowledge of Good Manufacturing Practices (GMP).
  • Ability to lead operational teams.
  • Intermediate to advanced English level.
  • Experience with Quality tools (GMP), including deviation investigation, root cause analysis, change control, CAPA, validation, and qualification.
  • Knowledge of continuous improvement methodologies such as Lean Manufacturing and Six Sigma.
  • A proactive, organized, and results-oriented mindset.

______________________________________

Xavier Alejandro Granda Silva, the Hiring Manager

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