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Jobs at JenaValve Technology, Inc. (Now Hiring) — 12 open

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Senior Specialist, Regulatory Affairs (THV)

Irvine, California, United States · On-site

$95k–$95k/yr

Mid level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $95,000.00 - $95,000.00 SalaryJob Category: QA - Quality ControlJob Title: Senior Specialist, Regulatory Affair…

Skills: Regulatory Affairs, Medical Device Regulations, Technical Writing, Project Management, Post-Market Surveillance

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Manager, Regulatory Affairs (International)

Irvine, California, United States · On-site

$150k–$150k/yr

Senior$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $150,000.00 - $150,000.00 SalaryJob Title: Manager, Regulatory Affairs (International) Supervisor/Manager Title…

Skills: Regulatory Affairs, Global Filings, People Management, Medical Device Regulations, MDSAP

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Senior Technician, Facilities & Equipment (2nd Shift)

Irvine, California, United States · On-site

$27/hr–$27/hr

Mid level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: High SchoolSalary Range: $27.00 - $27.00 HourlyJob Title: Senior Technician, Facilities & Equipment Role Level: Individual Contributor Sup…

Skills: Preventative Maintenance, Equipment Calibration, Facility Management, GMP, Cleanroom Operations

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Technician, THV Sewing (2nd Shift)

Irvine, California, United States · On-site

$27/hr–$27/hr

Entry level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: ContractorEducation Level: High SchoolSalary Range: $27.20 - $27.20 HourlyJob Title: Technician, THV Sewing Technician I, THV Sewing Technician II, THV Sewing Techn…

Skills: Manual Dexterity, Microscope Operation, Sewing, Tissue Preparation, Cleanroom Protocols

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Senior Manager, Strategic/Upstream Marketing

Irvine, California, United States · On-site

$180k–$180k/yr

Senior$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $180,000.00 - $180,000.00 Salary/yearJob Category: MarketingJob Description Summary: The Senior Manager Strateg…

Skills: Strategic Marketing, Upstream Marketing, Clinical Education, Product Innovation, Portfolio Strategy

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Temp Associate Technician, THV Sewing (2nd Shift)

Irvine, California, United States · On-site

$24/hr–$24/hr

Entry level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: ContractorEducation Level: High SchoolSalary Range: $24.20 - $24.20 HourlyJob Title: Temp Associate Technician, THV Sewing Role Level: Individual Contributor Superv…

Skills: Manual Dexterity, Microscope Operation, Sewing Assembly, Tissue Preparation, GMP Compliance

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Technician, THV Tissue Processing (2nd Shift)

Irvine, California, United States · On-site

$26/hr–$26/hr

Entry level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: ContractorEducation Level: High SchoolSalary Range: $26.60 - $26.60 HourlyJob Title: Technician, THV Tissue Processing Technician I, THV Tissue Processing Technicia…

Skills: Tissue Processing, GMP, Cleanroom Protocols, Manual Dexterity, Quality Management System

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Temp Associate Technician, THV Tissue Processing (2nd Shift)

Irvine, California, United States · On-site

$23/hr–$23/hr

Entry level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: ContractorEducation Level: High SchoolSalary Range: $23.70 - $23.70 HourlyJob Title: Temp Associate Technician, THV Tissue Processing Role Level: Individual Contrib…

Skills: Tissue Processing, Cleanroom Protocols, GMP, GDP, Microscope Operation

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Manager, Product Safety Risk Management

Irvine, California, United States · On-site

$139k–$139k/yr

Senior$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $138,500.00 - $138,500.00 SalaryJob Title: Manager, Product Safety Risk Management Role Level: Individual Contr…

Skills: ISO 14971, Risk Management, Medical Device Regulations, Design Controls, Post-Market Surveillance

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Coordinator, Clinical Affairs

Irvine, California, United States · On-site

$29/hr–$29/hr

Entry level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $29.00 - $29.00 HourlyJob Title: Coordinator, Clinical Affairs Supervisor/Manager Title: Director, Clinical Aff…

Skills: Clinical Research Support, Regulatory Documentation, Quality Control, MS Office Suite, Written Communication

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Supervisor, THV Production

Irvine, California, United States · On-site

$80k–$90k/yr

Mid level$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: High SchoolSalary Range: $96,750.00 - $96,750.00 SalaryJob Title: Supervisor, THV Production Role Level: People Manager Supervisor/Manager…

Skills: Production Supervision, Lean Manufacturing, Six Sigma, Medical Device Compliance, People Management

JenaValve Technology, Inc. logoJenaValve Technology, Inc.

Senior Specialist, Environmental Health & Safety

Irvine, California, United States · On-site

$105k–$105k/yr

Senior$342M raised

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $105,000.00 - $105,000.00 SalaryJob Title: Senior Specialist, Environmental Health & Safety Role Level: Individ…

Skills: EH&S Program Management, Regulatory Compliance, Risk Assessment, Incident Investigation, Industrial Hygiene

JenaValve Technology, Inc. logo

Senior Specialist, Regulatory Affairs (THV)

JenaValve Technology, Inc.

Irvine, California, United States • On-site

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Mid level

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  • $95k–$95k/yr
  • Full-time
  • bachelor degree
  • Posted 2d ago
  • ~40 hrs/week

Responsibilities

Responsible for global regulatory affairs communication, negotiation, and the preparation of pre-market and post-market submissions. The role involves managing serious adverse event reporting and ensuring product labeling complies with global regulations.

Requirements

Requires a Bachelor's degree in a scientific discipline and 3 to 5 years of experience in medical device Regulatory Affairs. Experience with US Class III cardiovascular devices is preferred.

Full job description

Job DetailsJob Location: Irvine, CA 92618Position Type: Full TimeEducation Level: 4 Year DegreeSalary Range: $95,000.00 - $95,000.00 SalaryJob Category: QA - Quality ControlJob Title: Senior Specialist, Regulatory Affairs

Role Level: Individual Contributor

Supervisor/Manager Title: Senior Manager, Regulatory Affairs

Job Location & Environment: Irvine, CA – Corporate Office Environment

Job Description Summary: Responsible for global regulatory affairs communication, regulatory negotiation and correspondence tracking, serious adverse event reporting, post-market surveillance, competitive intelligence, and maintenance of standards program. Under supervision, prepares clinical, pre-market and post-market submissions and query response development and communicates with regulatory authorities and partners. Provides expertise in translating regulatory requirements into practical, workable plans. Provides counsel to project teams as applicable. Ensures timely preparation of organized and scientifically valid submissions. Interacts with internal departments and external representatives (i.e., distributors, legal agents, regulatory agencies).

Job Responsibilities

Under supervision, lead the preparation, submission, and maintenance of high-quality global filings for investigational device authorizations and registrations, annual reports, and amendments/supplements, communicating with regulatory authorities as applicable.
Serve as the regulatory team member of product development and sustaining teams, providing clear direction and input to assure that applicable global requirements are incorporated in the development process and to drive attainment of company objectives.
Interpret existing or new regulatory requirements as they relate to company products and procedures, labeling, marketing projects, clinical studies, testing, or record keeping.
Manage and oversee submission of serious adverse event reporting, Medical Device Reports (MDRs), Vigilance reports, field safety notices, and other communication with competent authorities and other external stakeholders.
Review and approve FMEAs/risk analyses, protocols, reports, other technical documents.
Review product labeling for compliance with global labeling regulations.
Maintain regulatory intelligence through continuous monitoring of regulatory landscape.
Review and approve document change orders and prepare letters-to-file.
Update departmental procedures as required.
Produce monthly reports on global activities, issues, recommendations, and plans going forward.
Participate in external audits as needed.
Perform other duties as assigned by supervisor.

QualificationsRequired Education and Experience

Experience in applying global medical device regulations and product development process
Comprehensive knowledge of quality systems and relationship to business
Ability to interpret regulatory standards and guidance and provide direction to project teams
Ability to work in a fast-paced, technically challenging environment where drive is critical to success.
Self-motivated and self-disciplined; able to prioritize multiple tasks and responsibilities.
Effective interpersonal skills/diplomacy and problem-solving techniques.
Excellent applied thinking and technical writing skills.
Strong communication and organization skills required.
Bachelor’s degree in a scientific discipline or equivalent is required.
Minimum of 3 to 5 years in medical device Regulatory Affairs or other relevant experience.
Experience with US Class III cardiovascular devices preferred.

Skills and Abilities Required for This Job

Strong verbal and written communication, organization, and project management skills required.
Diplomacy and cultural sensitivity are essential attributes.
Works on problems of diverse scope and analyzes data and information to make sound decisions, recommendations, and regulatory filings of high quality.
Exercises good judgment within generally defined practices and policies in all aspects of the job.
Normally receives no instruction on routine work, and general instructions on new assignments.

Core Competencies

Customer Focus: Solicit and apply feedback from internal and external customers; Understand customers’ current and future expectations; Respond promptly to customer needs.
Innovation: Develop and champion unique ideas and solutions; Find new ways to use technology more effectively; Promote continuous learning.
Interdependent Partnering: Contribute to a productive and cooperative atmosphere; Show commitment to team objectives; Contribute own fair share of effort.
Master Complexity: Competently handle day-to-day work challenges; Thrive in uncertain circumstances; Adapt to changes in the work environment; Manage multiple tasks and competing demands; Change approach or method to best fit the situation.
Organizational & People Development: Function as both team player and leader; Provide informal feedback; Challenge the status quo; Strive for continuous professional development; Recognize the contributions of others; Set and achieve challenging goals.
Spoken Communication: Speak clearly and concisely; Listen carefully and seek clarification; Deliver effective presentations.
Written Communication: Write clearly and informatively; Create documents that are complete and accurate.
Commitment: Strive to attain quality results on time; Convey a sense of urgency and drive issues to closure; Earn a reputation for reliability and dependability.
Decisions: Make timely and sound decisions; Take risks and manage them intelligently.
Problem Solving: Proactively seek solutions; Gather and analyze information systematically; Develop alternative solutions; Think analytically and act decisively.
Diversity: Respond with sensitivity to people of diverse perspectives, ideas, backgrounds, lifestyles, and ages; Foster open communication and respect for the individual.
Equipment Use: Copy machines, personal computers, and computer terminals.
Computer Skills: Software proficiency in Microsoft Office Suite.
Language Skills: Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, legal documents, or governmental regulations. Ability to write reports, business correspondence, and procedure manuals. Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.
Mathematical Skills: Ability to work with mathematical concepts such as probability and statistical inference.
Reasoning Ability: Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.

Physical Requirements

Up to 20% travel required and ability to travel OUS.
Ability to occasionally lift and/or move up to 20 pounds.

Related keywords

Regulatory AffairsMedical DevicesClass III DevicesCardiovascular DevicesInvestigational Device AuthorizationsMDRVigilance ReportsFMEAGlobal LabelingQuality SystemsRegulatory IntelligenceTechnical DocumentationPost-Market SurveillanceClinical SubmissionsCorporate OfficeMicrosoft Office Suite

About JenaValve Technology, Inc.

LinkedInVisit site

Aortic regurgitation is different. So is our valve.

Industry
Medical Equipment Manufacturing
Company size
51-200 employees
Founded
2013
Headquarters
Irvine, CA
LinkedIn followers
16,578
Total funding
$342M

JenaValve is a medical device company developing the first transcatheter heart valve technology that is uniquely designed for the minimally invasive treatment of aortic regurgitation (AR). The JenaValve Trilogy Heart Valve System is the first and only device currently approved in the EU for the treatment of severe, symptomatic aortic regurgitation in patients that are deemed high-risk for surgical aortic valve replacement. The Trilogy System is also CE-Mark approved for treatment of severe, symptomatic aortic stenosis. In the US, JenaValve has completed enrollment of the ALIGN-AR IDE Clinical Trial which will support a future PMA submission. If approved, the Trilogy System would become the first and only TAVR system in the US indicated for the treatment of symptomatic, severe AR. JenaValve is headquartered in Irvine, California with offices in Leeds, U.K. and Munich, Germany.

Offices: 4 Cromwell, Suite 100, Irvine, CA 92618, US

Health CareMedical DeviceMedicalManufacturing
View all jobs at JenaValve Technology, Inc.

About JenaValve Technology, Inc.

LinkedInVisit site

Aortic regurgitation is different. So is our valve.

Industry
Medical Equipment Manufacturing
Company size
51-200 employees
Founded
2013
Headquarters
Irvine, CA
LinkedIn followers
16,578
Total funding
$342M

JenaValve is a medical device company developing the first transcatheter heart valve technology that is uniquely designed for the minimally invasive treatment of aortic regurgitation (AR). The JenaValve Trilogy Heart Valve System is the first and only device currently approved in the EU for the treatment of severe, symptomatic aortic regurgitation in patients that are deemed high-risk for surgical aortic valve replacement. The Trilogy System is also CE-Mark approved for treatment of severe, symptomatic aortic stenosis. In the US, JenaValve has completed enrollment of the ALIGN-AR IDE Clinical Trial which will support a future PMA submission. If approved, the Trilogy System would become the first and only TAVR system in the US indicated for the treatment of symptomatic, severe AR. JenaValve is headquartered in Irvine, California with offices in Leeds, U.K. and Munich, Germany.

Offices: 4 Cromwell, Suite 100, Irvine, CA 92618, US

Health CareMedical DeviceMedicalManufacturing
View all jobs at JenaValve Technology, Inc.

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