Operations Excellence Specialist Role Overview
This critical role is responsible for driving operational efficiency and excellence to positively impact lives globally.
* Ensure that all operations meet stringent regulatory requirements.
* Contribute to the development and execution of comprehensive audit programs.
* Prepare, review, and approve key operational documents.
* Serve as a subject matter expert to support strategic quality oversight.
* Deliver training on essential operational principles.
* Manage and maintain the organization's Quality Management System.
* Coordinate high-impact quality initiatives.
* Collaborate on strategic quality projects to drive continuous improvement.
To excel in this position, you will require:
* A degree in Pharmaceutical Sciences, Chemical Engineering, or a related field.
* A minimum of 3-5 years of experience in a similar role or within a GMP-operational setting.
* In-depth knowledge of quality management, cGMP, cGDP, and ICH guidelines.
* Experience working in an FDA-approved manufacturing environment is highly valued.
* Exceptional communication skills and the ability to foster strong partnerships with internal and external stakeholders.
* An analytical mindset with attention to detail.
* The capacity to prioritize tasks and resolve complex problems efficiently.
* A willingness to adapt to dynamic and fast-paced environments.
This opportunity offers a chance to be part of innovative projects and work alongside passionate colleagues who are driven to overcome challenges and make a lasting impact.