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Director, Regulatory Affairs (Animal Health)

Alveo TechnologiesAlameda, California, United StatesHybrid, Onsite

About Alveo


Alveo Technologies is the first company to make molecular detection and diagnostics universally accessible – on the farm, in the field, in the clinic, or in the manufacturing plant – helping prevent or significantly limit the destructive impact of viruses, fungi, bacteria, and other pathogens by detecting earlier at the Point of Need™. Alveo’s rugged and portable, multiplex-capable diagnostic platform employs IntelliSense™, its patented method of direct electrical sensing of nucleic acid amplification to provide affordable, rapid, and accurate results.

By enabling early pathogen detection, Alveo helps manage global health, food security, and supply chain resiliency by providing actionable insights at lightspeed. Know Sooner, Act Faster™ with Alveo. For more, visit: https://www.alveotechnologies.com/Alveo Technologies is looking for a dynamic highly skilled regulatory affairs professional. You are a clear and articulate communicator and a great listener and observer that can work effectively with other teams across the organization. In this role, you will combine regulatory, scientific and veterinary diagnosticexpertise to develop and execute regulatory strategies to ensure the successful approval and compliance of our products in the global market.

Your expertise in USDA CVB regulations and international veterinary diagnostic requirements will be instrumental in shaping our regulatory pathway. You will collaborate cross-functionally to support product development, registration, and post-market compliance while maintaining strong relationships with regulatory authorities. 

Key Responsibilities:


Regulatory


Strategy Development


Design and execute regulatory strategies to support the development, registration, and commercialization of veterinary diagnosticsProvide regulatory guidance to R&D, Quality Assurance, and Clinical Affairs to ensure compliance with applicable standards and guidelinesAnticipate regulatory challenges and develop risk-mitigation strategies to accelerate approval timelines 

Regulatory Submissions and Approvals


Lead the preparation, submission, and lifecycle management of regulatory dossiers to USDA CVB and other global regulatory agenciesEnsure timely submission and approval of product licenses, manufacturing licenses, and supplemental applicationsMaintain expertise in VS Memoranda, CVB policies and other applicable guidance impacting veterinary diagnostics

Regulatory Compliance


and Policy Monitoring


Monitor global regulatory trends and policy updates, ensuring internal compliance with USDA CVB, APHIS, and international regulatory frameworks Maintain up to date knowledge of regulatory changes and communicate their impact to the organization Support regulatory inspections and audits, providing necessary documentation and support, and drive continuous compliance improvements

Cross functional Collaboration


Work closely with R&D, Quality Assurance, Clinical Affairs, and Commercial Marketing teams to integrate regulatory considerations throughout the product lifecycleSupport regulatory training initiatives, ensuring teams remain up to date on compliance requirements

Technical


Documentation and Communication


Develop and maintain regulatory policies, SOPs and technical documentation to support regulatory submissions and auditsProvide regulatory content for design history files and maintain compliance documentationEffectively communicate with regulatory authorities, responding to inquiries, represent the company in meetings and negotiations

Qualifications


:


Minimum of a bachelor's degree in life sciences or veterinary medicineMinimum of 10 years previous experience in regulatory affairs with a focus on veterinary diagnosticsAn depth knowledge of regulatory requirements for US, EU, MENA, and other international geographiesDeep expertise in USDA CVB regulatory pathways and guidance documents, including experience with product development, licensure, and post-approval complianceProblem solving skills and the ability to get to yes or no quickly Excellent communication and teamwork skills, and the ability to adapt and interface effectively with a wide range of stakeholdersTravel 0 - 10%  Salary range is $196,686 - $205,000 per yearWe are an equal opportunity employer and value diversity at Alveo Technologies.

We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.Apply for this job

Life at Alveo Technologies

In today's interconnected world, we are currently faced with many global challenges and opportunities surrounding infectious diseases. At Alveo, we're tackling these head-on by creating technology platforms that provide rapid, reliable, and economical cloud-based diagnostics for use by everyone, anytime, everywhere.
Thrive Here & What We Value1. Emphasis on innovation and transformation2. Agile and dynamic diagnostic platform3. Global patented pathogen identification and diagnostic platform4. Rapid identification and diagnosis of a broad range of pathogens in people, animals, crops, and environmental systems5. Empowers the world to Know Sooner, Act Faster™
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