... medical devices.
60 Katalyst Medical Research Jobs Hiring Near You
... medical devices.
Strong experience in medical device development within a design controls environment. * Experience with catheter-based and/or single-use medical devices. * Proven ability to lead technical ...
Strong experience in medical device development within a design controls environment. * Experience with catheter-based and/or single-use medical devices. * Proven ability to lead technical ...
Strong experience in medical device development within a design controls environment. * Experience with catheter-based and/or single-use medical devices. * Proven ability to lead technical ...
Strong experience in medical device development within a design controls environment. * Experience with catheter-based and/or single-use medical devices. * Proven ability to lead technical ...
Strong experience in medical device development within a design controls environment. * Experience with catheter-based and/or single-use medical devices. * Proven ability to lead technical ...
Strong experience in medical device development within a design controls environment. * Experience with catheter-based and/or single-use medical devices. * Proven ability to lead technical ...
They will support clinical research teams by facilitating the study start-up approval process and ... medical licenses. * Develop and maintain electronic regulatory files in compliance with ...
They will support clinical research teams by facilitating the study start-up approval process and ... medical licenses. * Develop and maintain electronic regulatory files in compliance with ...
Quality Engineer
Lake Forest, CA · On-site
$75K - $98K/yr
Job Summary: * We are seeking a Quality Engineer with experience in the Medical Device industry to support innovative healthcare products while collaborating with R&D, Regulatory, and cross ...
Quality Engineer
Lake Forest, CA · On-site
$75K - $98K/yr
Job Summary: * We are seeking a Quality Engineer with experience in the Medical Device industry to support innovative healthcare products while collaborating with R&D, Regulatory, and cross ...
Minimum 5+ years of experience in the Medical Device domain. * Strong experience in Testing, Automation, and Test Method Development. * Experience with Prototype Development and 3D Printed Fixtures.
Minimum 5+ years of experience in the Medical Device domain. * Strong experience in Testing, Automation, and Test Method Development. * Experience with Prototype Development and 3D Printed Fixtures.
They will support clinical research teams by facilitating the study start-up approval process and ... medical licenses. * Develop and maintain electronic regulatory files in compliance with ...
They will support clinical research teams by facilitating the study start-up approval process and ... medical licenses. * Develop and maintain electronic regulatory files in compliance with ...
They will support clinical research teams by facilitating the study start-up approval process and ... medical licenses. * Develop and maintain electronic regulatory files in compliance with ...
They will support clinical research teams by facilitating the study start-up approval process and ... medical licenses. * Develop and maintain electronic regulatory files in compliance with ...
Epidemiologist (RWE)
Avenel, NJ · Remote
... observational research. * Responsibilities will include preparing study concepts, maintaining ... Collaborate with biostatistics, clinical, medical affairs, regulatory, and commercial teams to ...
Epidemiologist (RWE)
Avenel, NJ · Remote
... observational research. * Responsibilities will include preparing study concepts, maintaining ... Collaborate with biostatistics, clinical, medical affairs, regulatory, and commercial teams to ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
Senior Design Quality Engineer
$91K - $124K/yr
Ensure compliance with Design Controls and applicable medical device regulations. * Collaborate with R&D, Manufacturing, Regulatory Affairs, and Marketing teams to support product development and ...
Senior Design Quality Engineer
$91K - $124K/yr
Ensure compliance with Design Controls and applicable medical device regulations. * Collaborate with R&D, Manufacturing, Regulatory Affairs, and Marketing teams to support product development and ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
Coordinate and collect specific registration information with R&D, Quality, Medical, Manufacturing, etc. * Assess necessity for submitting a 510(k) application for proposed device changes. Prepare ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
Collaborate with R&D, Product Development, Quality, and Operations teams on NPI and Design Transfer ... Medical Device / Pharmaceutical Manufacturing. * Quality & Regulatory Compliance. * Engineering ...
Collaborate with R&D, Product Development, Quality, and Operations teams on NPI and Design Transfer ... Medical Device / Pharmaceutical Manufacturing. * Quality & Regulatory Compliance. * Engineering ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
... medical device manufacturing environment. This role will partner closely with R&D, Product Development, Manufacturing Engineering, Quality, and Operations teams to ensure products are designed for ...
Katalyst Jobs Information
What is it like to work at Katalyst?
Katalyst appears to be a collaborative and innovative company that values creativity and teamwork, fostering an environment where employees can share ideas and work together to achieve common goals.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
The company's structure and work environment seem to be designed to support a dynamic and agile approach, with a focus on delivering high-quality results and driving business growth. Katalyst's mission is centered around helping businesses and organizations succeed through strategic partnerships and tailored solutions.
Working at Katalyst may appeal to individuals who are passionate about innovation, collaboration, and making a meaningful impact in their industry, as the company offers opportunities for professional growth, skill development, and contributions to a dynamic and forward-thinking organization.
What makes Katalyst an attractive place to work?
Katalyst is a forward-thinking company that has established itself as a leader in its industry, known for its commitment to innovation and customer satisfaction. The company's work environment is characterized by a collaborative and dynamic atmosphere, where employees are encouraged to share ideas and work together to drive progress. Joining Katalyst offers opportunities for professional growth and development, as well as the chance to contribute to meaningful projects that can have a lasting impact.
What are the most popular job types at Katalyst?
What are the most popular jobs at Katalyst?
What are the most popular categories at Katalyst?
Job description
Roles & Responsibilities:
• Demonstrated experience working under Design Controls and ISO 13485 / FDA QSR environments.
• Proven ability to conduct root cause analysis and support field driven corrective actions.
• Strong written and verbal communication skills, including the ability to translate clinical feedback into engineering actions.
• Ability to work independently, prioritize multiple issues, and lead crossfunctional technical efforts.
• Direct exposure to field action support, complaints investigations, or post market surveillance.
• Familiarity with human factors standards (IEC 62366), risk management (ISO 14971), and related FDA guidance.
• Experience working closely with clinicians, clinical engineers, or medical affairs teams.
Education & Experience:
• Bachelor's degree in engineering or related technical field (mechanical, biomedical, or equivalent).
• 5 to 6 years of medical device development experience, including sustaining or post market engineering surveillance.
• Experience with structural heart or transcatheter cardiovascular devices.
• Experience owning or supporting IFUs, user needs, or human factors engineering for Class III medical devices.
• Demonstrated experience working under Design Controls and ISO 13485 / FDA QSR environments.
• Proven ability to conduct root cause analysis and support field driven corrective actions.
• Strong written and verbal communication skills, including the ability to translate clinical feedback into engineering actions.
• Ability to work independently, prioritize multiple issues, and lead crossfunctional technical efforts.
• Direct exposure to field action support, complaints investigations, or post market surveillance.
• Familiarity with human factors standards (IEC 62366), risk management (ISO 14971), and related FDA guidance.
• Experience working closely with clinicians, clinical engineers, or medical affairs teams.
Education & Experience:
• Bachelor's degree in engineering or related technical field (mechanical, biomedical, or equivalent).
• 5 to 6 years of medical device development experience, including sustaining or post market engineering surveillance.
• Experience with structural heart or transcatheter cardiovascular devices.
• Experience owning or supporting IFUs, user needs, or human factors engineering for Class III medical devices.