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Micro Medical Device Jobs in Florida (NOW HIRING)

This role entails working in a medical device environment and applying Materials and Engineering ... Experience with micro-molding, mold design or overall injection molding is preferred * Working ...

Sr. Equipment Engineer

Kissimmee, FL · On-site

$79K - $119K/yr

... micro electro-mechanical systems and other emerging device topologies. We manufacture products for aerospace and defense, medical, automotive, consumer and industrial markets, to name a few. Our ...

New

Fab Operator

Kissimmee, FL · On-site

$16.62 - $24.92/hr

... micro electro-mechanical systems and other emerging device topologies. We manufacture products for aerospace and defense, medical, automotive, consumer and industrial markets, to name a few. Our ...

Showing results 21-40

Micro Medical Device information

What are the key skills and qualifications needed to thrive as a micro medical device engineer, and why are they important?

To thrive as a Micro Medical Device Engineer, you need expertise in biomedical engineering, microfabrication, and materials science, often with at least a bachelor's or master's degree in a related field. Familiarity with CAD software, cleanroom processes, and relevant regulatory standards such as ISO 13485 or FDA guidelines is typical. Strong problem-solving abilities, attention to detail, and effective teamwork are essential soft skills in this role. These competencies ensure the design, development, and manufacturing of safe, reliable, and innovative micro-scale medical devices for patient care.

What is a micro medical device?

Micro medical devices are extremely small tools or implants, often at the millimeter or even micrometer scale, designed for medical applications such as diagnostics, drug delivery, or minimally invasive surgeries. These devices leverage advanced materials and miniaturized technology to perform precise functions within the body, often accessing areas that are difficult to reach with traditional devices. Examples include micro-needles, implantable sensors, and tiny surgical instruments. The development of micro medical devices has improved patient outcomes by reducing recovery times and minimizing tissue damage.

What are some common challenges faced by professionals working in micro medical device development?

Professionals in micro medical device development often encounter challenges such as adhering to strict regulatory standards, ensuring biocompatibility and safety of miniature components, and managing the complexities of integrating advanced technologies at a micro scale. Collaboration with cross-functional teams—including engineers, clinicians, and regulatory experts—is crucial to address these challenges effectively. Additionally, staying updated with rapid advancements in materials science and manufacturing techniques is essential for success in this innovative field.

What is the difference between Micro Medical Device vs Medical Device Technician?

AspectMicro Medical DeviceMedical Device Technician
Required CredentialsTypically requires a biomedical or mechanical engineering degree or certificationRequires technical training or certification in medical device repair and maintenance
Work EnvironmentResearch labs, manufacturing facilities, or quality control settingsHospitals, clinics, or repair centers
Employer & Industry UsageMedical device manufacturing companies, biotech firmsHospitals, medical equipment service companies
Common Search & Comparison IntentUnderstanding roles in medical device developmentMaintenance and repair of medical equipment

Micro Medical Device professionals focus on designing and developing tiny medical devices, often requiring engineering expertise. Medical Device Technicians primarily handle the maintenance, repair, and calibration of medical equipment used in healthcare settings. While both roles are integral to the medical device industry, they differ in responsibilities, work environments, and required credentials.

What cities in Florida are hiring for Micro Medical Device jobs? Cities in Florida with the most Micro Medical Device job openings:

Injection Molding Process Engineer

Jj

Jacksonville, FL • On-site

Full-time

Posted 11 days ago


Job description

At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com.

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:

R&D Product Development

Job Sub Function:

Biomedical Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Anasco, Puerto Rico, United States of America, Jacksonville, Florida, United States of America

Job Description:

Johnson & Johnson Vision, Inc. is currently hiring a Materials Engineer, to join its dynamic team located in Anasco, PR.

The Engineer is directly responsible for leading multiple raw material and molding related projects for the manufacture of inter-ocular lenses (IOL) at our site. They will lead multi-functional project teams and ensure that projects are completed on time and within budget. The Engineer will be an integral member of the Materials Engineering team in Anasco, PR and be fully accountable for Business Continuity, Validations, Cost Improvement and Supplier Enabled Innovation/Process Changes. The candidate should be able to possess an ability to work with peers and collaborators to enable the delivery of strong results.

The candidate will possess a technical understanding of injection molding, polymer materials, validations and mold fabrication.

The role collaborates with key business partners including Procurement, R&D, Supplier Quality, Engineering, Operations, Quality Assurance, and Regulatory Affairs to deliver on objectives. This role entails working in a medical device environment and applying Materials and Engineering knowledge to deliver innovative solutions to the business, both internally and at external supplier manufacturing sites through feasibility and scale-up. They will act as an advocate for continuous improvement of technology and processes, minimizing lifecycle costs, and adhering to environmental policies and procedures.

Key Responsibilities:

Accountable for molding/resin characterizations/qualifications, developing/updating the appropriate specifications and supporting regulatory submission documentation/inquires. This includes:

  • Conducting risk assessments and leading detailed product / process design reviews
  • Develop project and qualification plans to lead projects to meet timelines and budgets
  • Apply appropriate statistical and validation techniques based on overall risk

Responsible for identifying, coordinating, planning, executing, and evaluating value improvement projects at key, strategic materials suppliers to ensure quality, and on-time delivery. This entails:

  • Implementation of cost-effective manufacturing solutions to drive end-to-end manufacturing efficiencies in collaboration with procurement and strategic suppliers
  • Responsible for technical direction of supplier changes in partnership with Supplier Quality
  • Conduct feasibility studies to assess new technologies or process improvements

Qualifications:

  • Minimum of a Bachelor's degree in Plastics Engineering, Mechanical Engineering, Materials Science or equivalent engineering is required. Advanced degree (MS, PhD, MBA) is preferred.
  • Relevant work experience is required.
  • Ability to use and navigate AutoCad/Inventor is highly desirable.
  • Candidate must speak fluent English
  • Excellent written and oral communication skills required.
  • Excellent interpersonal skills required.
  • This position requires candidate to be onsite and is located Anasco, PR.
  • Must have the ability to work on own initiative and be able to lead multiple priorities simultaneously requiring excellent organizational skills.
  • Must be flexible, occasionally different work schedules are needed to support project needs.
  • Achievement of Six Sigma/Green Belt/Black Belt accreditation is preferred.
  • Experience/familiarity with an FDA-regulated medical device or pharmaceuticals industry is preferred.
  • Experience with troubleshooting, non-conformances, validations is preferred.
  • Occasionally, a project may require travel for support. This position may require up to 15% travel.
  • Experience qualifying (Validation & Risk Assessments) materials or processes in automated manufacturing environment is desirable
  • Experience with micro-molding, mold design or overall injection molding is preferred
  • Working experience with external suppliers to include partnering internationally is preferred

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson and Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, please email the Employee Health Support Center (ra-employeehealthsup@its.jnj.com) or contact AskGS to be directed to your accommodation resource.

Required Skills:

Preferred Skills:

Bioinformatics, Biological Engineering, Biological Sciences, Biostatistics, Data Reporting, Data Savvy, Design of Experiments (DOE), Detail-Oriented, Execution Focus, Feasibility Studies, Preclinical Research, Problem Solving, Process Oriented, Prototyping, Report Writing, Research and Development, Researching, SAP Product Lifecycle Management, Technologically Savvy