Support management, investigation, escalation, and resolution of EU FMD alerts in coordination with internal stakeholders, CMOs, EMVO-connected partners, and external service providers. * Maintain ...
Support management, investigation, escalation, and resolution of EU FMD alerts in coordination with internal stakeholders, CMOs, EMVO-connected partners, and external service providers. * Maintain ...
Support management, investigation, escalation, and resolution of EU FMD alerts in coordination with internal stakeholders, CMOs, EMVO-connected partners, and external service providers. * Maintain ...
Support management, investigation, escalation, and resolution of EU FMD alerts in coordination with internal stakeholders, CMOs, EMVO-connected partners, and external service providers. * Maintain ...
Emvo information
What is an Emvo?
EMVO stands for the European Medicines Verification Organisation. It is a non-profit organization responsible for implementing and managing the European Medicines Verification System (EMVS), which helps prevent counterfeit medicines from entering the supply chain. EMVO works with pharmaceutical manufacturers, wholesalers, and pharmacies to ensure that all prescription medicines sold in the EU are safe and authentic. Their primary role is to oversee the secure operation of the system, provide guidance to stakeholders, and ensure regulatory compliance.
What does an Emvo do?
It appears that 'Emvo' is not recognized as a standard professional job title in the current job market. If you meant a different position or a specific acronym, please double-check the spelling or provide more context. This will help ensure you receive relevant and accurate information about the role you are interested in.
What are the key skills and qualifications needed to thrive as an EMVO specialist?
To thrive as an EMVO specialist, you typically need a background in pharmaceutical regulations, quality assurance, and supply chain management, often supported by relevant degrees or experience in life sciences or regulatory affairs. Familiarity with serialization systems, traceability software, and knowledge of the EU Falsified Medicines Directive are essential technical requirements. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure compliance and facilitate collaboration with stakeholders. These competencies are crucial for safeguarding pharmaceutical integrity and meeting regulatory obligations within the European medicines verification framework.
What is the difference between Emvo vs Paramedic?
| Aspect | Emvo | Paramedic |
|---|---|---|
| Required Credentials | EMVO certification, basic life support | EMT certification, advanced life support |
| Work Environment | Emergency medical services, pre-hospital care | Ambulance, hospital emergency departments |
| Industry Usage | Pre-hospital emergency response | Pre-hospital and hospital emergency care |
Emvo and Paramedic roles both involve emergency medical response, but Emvo typically requires basic certification and focuses on initial patient assessment and transport, while Paramedics have advanced training for complex procedures. Both work in emergency settings, but Paramedics often perform more advanced interventions.
What are popular job titles related to Emvo jobs in California?
For Emvo jobs in California, the most frequently searched job titles are:
What job categories do people searching Emvo jobs in California look for?
The top searched job categories for Emvo jobs in California are:
What cities in California are hiring for Emvo jobs?
Cities in California with the most Emvo job openings:
Senior Manager, Commercial Supply Chain Serialization & Traceability
Redwood City, CA • On-site
Full-time
Posted 12 days ago
Job description
The Opportunity
We are seeking an experienced Senior Manager, Commercial Supply Chain, Serialization & Traceability to lead global serialization and traceability capabilities supporting commercial product launches and lifecycle management activities. This role is responsible for supporting compliant and scalable serialization operations across global supply networks, including CMOs, packaging sites, wholesalers, 3PLs, and external service providers. The ideal candidate will bring hands-on experience supporting or leading global serialization implementations, including EU FMD operational readiness, EPCIS data exchange, aggregation, and downstream trading partner connectivity. This role partners cross-functionally with Supply Chain, Quality, Regulatory, Packaging, Manufacturing, and IT teams to ensure compliant execution of global traceability requirements, including DSCSA, EU FMD, and emerging international regulations.
Key Responsibilities
Serialization & Traceability Operations
Lead serialization and traceability operational readiness activities supporting commercial launches and ongoing supply operations.
Support implementation and operationalization of global serialization and traceability requirements, including DSCSA, EU FMD, and emerging international regulations.
Support management, investigation, escalation, and resolution of EU FMD alerts in coordination with internal stakeholders, CMOs, EMVO-connected partners, and external service providers.
Maintain and support global GS1 registration activities, including management of company prefixes, GTIN structures, GLNs, and associated product identification data supporting serialization and traceability operations.
Maintain oversight of serialized product onboarding, aggregation strategies, and downstream trading partner readiness activities.
Serve as a subject matter expert for serialization operations, EPCIS data exchange, and global traceability requirements.
Approve serialized commercial artwork, labeling implementation, and packaging change management activities.
Serialized Data Governance & Partner Management
Oversee serialized data exchange processes among CMOs, packaging sites, logistics providers, wholesalers, and external trading partners.
Support investigation and resolution of serialization data exchange issues, failed transmissions, aggregation discrepancies, and connectivity exceptions.
Support operational metrics and dashboards related to serialization health, partner readiness, and data integrity.
Partner with CMOs, 3PLs, wholesalers, and serialization service providers to ensure operational readiness and ongoing compliance.
Compliance, Documentation, & Cross-Functional Leadership
Author and maintain serialization and traceability SOPs, work instructions, business processes, and associated documentation.
Maintain serialization and traceability procedures, work instructions, and business process documentation.
Own change controls and risk assessments and support audits, inspections, investigations, CAPAs, associated with serialization processes and systems.
Serve as a central coordination point between Supply Chain, Quality, Regulatory, Packaging, Manufacturing, and IT teams for serialization and traceability initiatives.
Support commercial launch readiness activities and continuous improvement initiatives associated with digital supply chain and traceability capabilities.
Able to operate effectively and with a strong sense of urgency in a fast-paced environment.
Required Skills, Experience and Education:
Bachelor's degree in Supply Chain, Engineering, Life Sciences, Information Systems, or related field.
8+ years of experience in pharmaceutical supply chain operations, including serialization, traceability, or commercial operations experience.
Familiarity with serialization platforms such as TraceLink, SAP ATTP, rfxcel, or Systech and EPCIS data exchange processes and GS1 standards, including SGTIN, SSCC, GLN, and aggregation hierarchies.
Strong knowledge of global serialization and traceability requirements, including DSCSA and EU FMD.
Strong cross-functional leadership, communication, organizational, and problem-solving skills.
Experience supporting serialized product onboarding and global trading partner connectivity across CMOs, wholesalers, packaging sites, and external partners.
Preferred Skills
Direct experience supporting or leading implementation of EU FMD serialization and traceability requirements within a commercial pharmaceutical environment.
Direct experience resolving EU FMD alerts, driving investigations, and coordinating activities across internal teams, CMOs, EMVO-connected partners, and external stakeholders.
Deep knowledge of ERP systems, product master data structures, packaging hierarchies, and data governance processes supporting serialization operations.
Experience managing serialized commercial artwork, labeling implementation, and packaging change management activities within a regulated pharmaceutical environment.
GS1 Healthcare or DSCSA-related certification.
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