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Terumo Jobs in Florida (NOW HIRING)

Terumo Corporation

Director, Manufacturing

Sunrise, FL · On-site

At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to ...

Terumo Corporation

Director, Manufacturing

Sunrise, FL · On-site

At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to ...

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Terumo information

What is Terumo and what does the company do?

Terumo is a global medical technology company headquartered in Japan, specializing in the development, manufacturing, and distribution of medical devices and supplies. The company offers products and solutions in fields such as vascular intervention, cardiothoracic surgery, transfusion medicine, and hospital products. Terumo is known for innovations like syringes, catheters, and blood management systems, serving hospitals, clinics, and healthcare professionals worldwide. Their mission focuses on contributing to society through healthcare by delivering high-quality, reliable medical products.

What are the key skills and qualifications needed to thrive as a medical device sales representative at Terumo?

To thrive as a Medical Device Sales Representative at Terumo, you need strong knowledge of medical products, sales techniques, and a bachelor’s degree in a related field. Familiarity with CRM systems, healthcare regulations, and product demonstration tools is typically required. Excellent communication, relationship-building, and problem-solving skills help foster trust with clients and healthcare professionals. These abilities are crucial for driving sales growth, ensuring compliance, and maintaining long-term partnerships in a highly competitive industry.

What are some common challenges faced by employees working at Terumo in the medical device industry?

Employees at Terumo often encounter challenges such as keeping up with evolving regulatory requirements, ensuring strict quality control, and adapting to rapidly advancing medical technologies. Additionally, cross-functional collaboration is essential, as teams frequently work with colleagues in R&D, manufacturing, and sales to bring new products to market. Navigating these dynamics requires strong communication, adaptability, and a commitment to continuous learning, which Terumo actively supports through training and professional development opportunities.

What is the difference between Terumo vs Cardiology Technician?

AspectTerumoCardiology Technician
Required CertificationsVaries by role, often includes medical device trainingCPR, Basic Life Support (BLS), and specialized cardiology certifications
Work EnvironmentMedical device manufacturing, hospital settings, clinicsHospitals, clinics, cardiology labs
Industry UsageMedical device manufacturing and salesPatient care, diagnostic testing, equipment operation

While Terumo focuses on manufacturing and supplying medical devices, Cardiology Technicians primarily work directly with patients and diagnostic equipment in clinical settings. Both roles require healthcare knowledge, but their daily tasks and work environments differ significantly.

Does Terumo have entry level positions?

Terumo offers entry-level positions across various departments, including manufacturing, sales, and research. These roles typically require minimal prior experience and may involve on-the-job training or certifications. Entry-level opportunities are suitable for recent graduates or individuals seeking to start a career in medical device manufacturing or healthcare technology.

Is Terumo a good place to work?

Terumo is a global medical device company known for a collaborative work environment and opportunities for professional development. Employees often cite competitive benefits and a focus on innovation, though experiences can vary by location and role.

What is it like to work at Terumo?

Working at Terumo involves a professional environment focused on medical device manufacturing and healthcare solutions. Employees often work in teams, require attention to detail, and may need technical skills or certifications depending on the role. The company emphasizes quality, safety, and innovation in its operations.

What are popular job titles related to Terumo jobs in Florida?

For Terumo jobs in Florida, the most frequently searched job titles are:

What job categories do people searching Terumo jobs in Florida look for?

The top searched job categories for Terumo jobs in Florida are:

What cities in Florida are hiring for Terumo jobs?

Cities in Florida with the most Terumo job openings:

Terumo jobs near you
Infographic showing various Terumo job openings in Florida as of August 2026, with employment types broken down into 1% Internship, 84% Full Time, 5% Part Time, 2% Temporary, 4% Contract, and 4% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution.

Manager, Regulatory Affairs

Terumo Corporation

Sunrise, FL • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 8 days ago

Job description

At Terumo Aortic, our mission is to transform the treatment of aortic disease worldwide. With our comprehensive portfolio of surgical, endovascular and hybrid technologies, we enable physicians to find the right fit for each patient anatomy.

The company has over 1,250 associates around the world with manufacturing facilities in Glasgow, Scotland and Sunrise, Florida.

Terumo Aortic is focused on the continuing development of new and innovative products driving the growth of the business globally. Associates are part of a stimulating and exciting environment in which they can develop their skills and achieve career goals. Working for the company, each associate's role contributes greatly to helping to save or improve the lives of patients in over 100 countries worldwide.

At Terumo we believe in the power of personal growth and will encourage you to get in the driver's seat - progressing in the direction you want to go by deepening your skills throughout your career. We want you to be bold, think outside the box, experiment, innovate and deliver what's next for quality healthcare. You will be part of a collaborative, respectful and resilient team of associates and leaders around the world, working together as partners to achieve more than you thought possible, providing real-world, impactful solutions for patients.

Join us and help shape wherever we go next!

Advancing healthcare with heart

www.terumoaortic.com

Job Summary

Leads team to determine regulatory requirements and strategies for Terumo Medical Corporation and Terumo Corporation projects.  Team will define information and actions necessary to meet these requirements.  Oversees and assists in the preparation of documents and or submissions required to obtain clearance or approval from government agencies for commercial distribution of products worldwide. Serves as liaison between government agencies and Terumo.  Mistakes made in this area can be very costly, i.e., delays in product clearance or approval withdrawal of product from the market place, or enforcement of fines.  Any of the above would have a major impact on the corporation.

Job Details/Responsibilities
  • Associate is responsible to follow requirements of applicable national and international regulations.  Associate assists other Regulatory Associates in understanding how to interpret these regulations.  
  • Guides team in analyzing data received and preparing documentation for submission for the purpose of obtaining clearance and or approval for product.  
  • Participates on product design teams and verifies compliance with design control requirements and procedures. 
  • Determine appropriate regulatory requirements and strategies for TMC, TPC, TMPH, and TC projects including both domestic and foreign activities and provide regulatory consultation to other internal and external entities.  
  • Acquire and maintain a current knowledge of federal (US, Canadian, and Europe) regulations pertaining to the lawful distribution of products which include facility registration, device listing, labeling and promotional review.  
  • Maintain documentation and a historical record for projects and provide management with updated product status.    
  • Participate in task force groups and industry working groups.  
  • Maintains current knowledge of Federal USA and Canadian regulations pertaining to legal distribution of medical products.  
  • Stays abreast of FDA updates including new policies and guidance.
  • Interact with production division, federal agencies, industry organizations, interdepartmentally and external departments at all levels.
  • Assists external customers by supplying materials and documentation for US and foreign product registrations as well as certification of appropriate US commercialization status.
  • Makes a proactive contribution to the overall Regulatory affairs department growth.
  • Provides general regulatory consultation during absence of other associates.
  • Participates in project performance team meetings on behalf of the business unit in order to provide ideas, methods or processes for unit/company performance improvement.
  • Develop global regulatory strategies for high risk products and lead multidisciplinary project teams
  • Performs other job related duties as assigned.
Knowledge, Skills and Abilities (KSA)
  • Experience on Design Control project teams.  
  • Advanced ability for independent work, team work, and decision making
  • Able to lead and mentor RA associates regardless of location
  • Demonstrated the ability to make correct decisions based on interpretations of federal laws, which in many instances are very general in nature to accommodate a variety of industries.  These interpretations are used for every aspect of the regulatory discipline from submissions to labeling issues.
  • Demonstrated the ability to develop global regulatory strategies for high risk products and lead multidisciplinary project teams
  • Requires ability to complete internal update (letters to file) preparations independently and completion of at least five (5) during TMC employment (or equivalent at prior employment).
Qualifications/ Background Experiences
  • Typically requires a 4 year degree in life sciences 
  • 7 years of experience in Regulatory Affairs or a Masters in Regulatory Affairs and 5 years of experience.
  • Regulatory Affairs Certification preferred.
  • Pre-sub, IDE and/or PMA submission experience preferred.
  • Must have completed three (3) 510(k) submissions and demonstrated ability to prepare submissions independently.
  • Management experience (at least 2 years of project or supervisory management)
     

It is Terumo's policy to provide equal employment opportunity to all its employees and applicants for employment regardless of their race, creed, color, national origin, age, ancestry, nationality, marital or domestic partnership or civil union status, sex, pregnancy, gender identity or expression, disability status, liability for military service, protected veteran status, sexual orientation, atypical cellular or blood trait, genetic information (including the refusal to submit to genetic testing), or any other category protected by law. As a Company, we value diversity of background and opinion, and prohibit discrimination or harassment on the basis of any legally protected class in the areas of hiring, recruitment, promotion, transfer, demotion, training, compensation, pay, fringe benefits, layoff, termination or any other terms and conditions of employment.

Final compensation packages may be higher or lower than what is listed, and will ultimately depend on factors including relevant experience, internal equity, skillset, knowledge, geography, education, business needs and market demand. We provide competitive and comprehensive benefit options which include: annual bonus, paid vacation, paid holidays, health, dental and vision benefits, 401(k), with matching contributions, tax advantage savings accounts, legal plan, voluntary life and AD&D insurance, voluntary long-term disability, short term disability, critical illness and accident insurance, parental leave, personal leave, tuition reimbursement, travel assistance, and an employee assistance program.  Pay range: $119,040 - $163,680

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