Global Trade Operations Specialist

Katalyst CRO; Santa Rosa (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

Katalyst CRO is seeking a detail-oriented Global Trade Operations Specialist to support labeling operations for medical devices in California. The role requires collaboration across departments, compliance with global trade and labeling standards, and a strong understanding of manufacturing processes.

The ideal candidate will manage labeling activities, leverage LMD systems, and drive improvements while maintaining high levels of accuracy and regulatory awareness.

Qualifications

• Experience with labeling processes in the medical device industry.
• Knowledge of medical device manufacturing regulatory requirements.
• Experience with labeling systems such as LMD.
• Strong stakeholder management and communication skills.
• Excellent attention to detail and organizational abilities.

Responsibilities

• Support global trade operations, ensuring adherence to international regulations and company policies.
• Coordinate and manage labeling activities, including Labeling Management Database (LMD) processes.
• Collaborate with cross-functional teams and stakeholders to ensure timely and accurate execution of labeling requirements.
• Ensure compliance with regulatory standards related to medical device manufacturing and labeling.
• Identify process improvements to enhance operational efficiency and compliance.

Skills

Labeling processes

Regulatory compliance

Stakeholder management

Attention to detail

Cross-functional collaboration

Tools

Labeling Management Database (LMD)

Job description

Job Summary

We are seeking a detail-oriented Global Trade Operations Specialist to support global trade and labeling operations within the medical device industry. This role requires strong cross-functional collaboration, compliance expertise, and a solid understanding of labeling and manufacturing processes.

Job Summary

We are seeking a detail-oriented Global Trade Operations Specialist to support global trade and labeling operations within the medical device industry. This role requires strong cross-functional collaboration, compliance expertise, and a solid understanding of labeling and manufacturing processes.

Responsibilities

• Support global trade operations, ensuring adherence to international regulations and company policies.
• Coordinate and manage labeling activities, including Labeling Management Database (LMD) processes.
• Collaborate with cross-functional teams and stakeholders to ensure timely and accurate execution of labeling requirements.
• Ensure compliance with regulatory standards related to medical device manufacturing and labeling.
• Identify process improvements to enhance operational efficiency and compliance.

Required Qualifications

• Proven experience in labeling processes within the medical device industry.
• Strong knowledge of medical device manufacturing and regulatory requirements.
• Experience working with labeling systems such as LMD (Labeling Management Database).
• Excellent stakeholder management and communication skills.
• Strong attention to detail and organizational abilities.

Preferred Qualifications

• Experience supporting global trade or international operations.
• Familiarity with FDA and international regulatory guidelines.