DescriptionLocation
Colombia On-site at local 3PL facility
Why You Should Join Us
Join a team committed to ensuring the safety quality and compliance of lifechanging health this role you will play a vital part in releasing products to the Colombian market by ensuring they meet all quality regulatory and storage requirements. Youll collaborate closely with Quality Logistics Regulatory Affairs and our 3PL partners gaining experience in Good Storage Practices GxP and quality oversight within the healthcare sector.
This is a great opportunity for someone passionate about quality detailoriented work and contributing directly to patient safety.
What Youll Do
You will support product release activities and perform quality inspections for imported products. Key responsibilities include:
Quality Inspections & Documentation
- Perform product and process inspections at the 3PL facility following approved instructions and sampling plans.
- Review and maintain documentation related to labeling packaging returns and batch records to support product disposition.
- Ensure full product traceability through accurate and complete documentation.
- Monitor and verify compliance with GxP and GMP requirements executed by the 3PL.
Compliance & Regulatory Support
- Support creation and updates of labeling documentation in coordination with Regulatory Affairs.
- Track and follow up on local CAPAs and nonconformances to ensure timely completion of required actions.
- Monitor compliance with storage conditions for ASP products at the 3PL facility.
- Escalate any quality incidents or risks to the Market Quality Manager promptly.
Operational Excellence
- Prioritize inspection activities based on business needs while ensuring product quality and safety at all times.
- Collaborate with Logistics Global Trade and the local Logistics Operator to ensure smooth and compliant operations.
What You Bring
Must-Have
- Experience handling healthcare products ideally within medical devices pharmaceuticals or a similar regulated environment.
- Knowledge of Good Storage Practices and relevant local regulations.
- Strong attention to detail and commitment to accuracy.
- Ability to work independently while collaborating effectively with crossfunctional teams.
Nice-to-Have
- Technical or university degree (not required but considered a plus).
- Prior experience working in a 3PL or distribution quality environment.
- Familiarity with GxP GMP CAPA processes or quality management systems.
What Youll Get
- Competitive compensation package
- Comprehensive health insurance
- Paid vacation and holidays
- Opportunities for training and professional development
- Inclusive diverse and missiondriven work environment
- Ability to grow within Quality and Regulatory functions
#LI-NL1
#LI-Onsite
DescriptionLocationColombia On-site at local 3PL facilityWhy You Should Join UsJoin a team committed to ensuring the safety quality and compliance of lifechanging health this role you will play a vital part in releasing products to the Colombian market by ensuring they meet all quality regulatory ...
DescriptionLocation
Colombia On-site at local 3PL facility
Why You Should Join Us
Join a team committed to ensuring the safety quality and compliance of lifechanging health this role you will play a vital part in releasing products to the Colombian market by ensuring they meet all quality regulatory and storage requirements. Youll collaborate closely with Quality Logistics Regulatory Affairs and our 3PL partners gaining experience in Good Storage Practices GxP and quality oversight within the healthcare sector.
This is a great opportunity for someone passionate about quality detailoriented work and contributing directly to patient safety.
What Youll Do
You will support product release activities and perform quality inspections for imported products. Key responsibilities include:
Quality Inspections & Documentation
- Perform product and process inspections at the 3PL facility following approved instructions and sampling plans.
- Review and maintain documentation related to labeling packaging returns and batch records to support product disposition.
- Ensure full product traceability through accurate and complete documentation.
- Monitor and verify compliance with GxP and GMP requirements executed by the 3PL.
Compliance & Regulatory Support
- Support creation and updates of labeling documentation in coordination with Regulatory Affairs.
- Track and follow up on local CAPAs and nonconformances to ensure timely completion of required actions.
- Monitor compliance with storage conditions for ASP products at the 3PL facility.
- Escalate any quality incidents or risks to the Market Quality Manager promptly.
Operational Excellence
- Prioritize inspection activities based on business needs while ensuring product quality and safety at all times.
- Collaborate with Logistics Global Trade and the local Logistics Operator to ensure smooth and compliant operations.
What You Bring
Must-Have
- Experience handling healthcare products ideally within medical devices pharmaceuticals or a similar regulated environment.
- Knowledge of Good Storage Practices and relevant local regulations.
- Strong attention to detail and commitment to accuracy.
- Ability to work independently while collaborating effectively with crossfunctional teams.
Nice-to-Have
- Technical or university degree (not required but considered a plus).
- Prior experience working in a 3PL or distribution quality environment.
- Familiarity with GxP GMP CAPA processes or quality management systems.
What Youll Get
- Competitive compensation package
- Comprehensive health insurance
- Paid vacation and holidays
- Opportunities for training and professional development
- Inclusive diverse and missiondriven work environment
- Ability to grow within Quality and Regulatory functions
#LI-NL1
#LI-Onsite
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