Address
Form of workThis position is eligible for a $5,000 sign on bonus
This is not a remote position
ABOUT THE COMPANY
More than just another design shop or contract manufacturer, Cirtec offers a uniquely comprehensive range of vertically integrated capabilities. Cirtec specializes in complex, difficult to produce components and devices in today's most advanced product technologies including, neuromodulation, implantable drug delivery, cardiac rhythm management, ventricular assist and interventional devices and delivery systems. We have the capabilities needed to bring products to full production, including assembly, packaging and testing, and in-house sterilization.
Our employees have the expertise needed to design innovative devices, solve complex design challenges, and help bring our customers' devices to market. If you are interested in working in a fun, challenging, fast-paced environment with a company that is growing and providing leading edge technology, Cirtec is the company for you!
YOU ARE A PART OF:
The engineering team consisting of other engineers with diverse backgrounds and expertise. The Engineering team works in close collaboration with Operations, R&D, and Purchasing. You will be involved in the design, development, documentation and validation of new customer products, and modification of existing products including defining requirements, timelines, and deliverables with a focus on prototypes, process development, design verification, clinical builds, training production, and preparation for process validation and manufacturing transfer of products.
JOB SUMMARY
The Engineer, Quality Design & Development is responsible for providing support to product development
teams and sustaining manufacturing/operations teams. This individual will be expected to apply design
control principles and techniques for medical devices. As a member of one or more cross-functional teams,
this individual will ensure products are designed and developed in accordance with applicable regulatory
requirements, customer requirements, and company policy.
ESSENTIAL RESPONSIBILITIES
• Perform Design Quality Engineering activities throughout the design, development, and production of
medical devices to ensure compliance to company's Design Control procedures and regulatory
requirements (specifically FDA 21 CFR 820 and ISO 13485).
• Create, review and/or approve technical Design Control documentation to facilitate design, development,
and product verification testing of medical devices in collaboration with cross-functional engineering teams.
• Create and execute Quality Plans for Product Design and Development projects.
• Represent Quality Engineering in technical design and phase end reviews.
• Develop and perform Design of Experiments (DOE).
• Develop and validate test methods.
• Develop sampling plans and acceptance criteria for product testing and inspection methods using
appropriate statistical techniques.
• Lead and/or participate in risk management activities, develop Risk Management Plans and Reports,
perform Hazards Analysis and FMEAs (Failure Mode Effects Analysis) to evaluate and ensure product
safety and functionality.
• Conduct and/or support root cause investigations, develop and implement corrective and preventative
actions for quality system and product related nonconformances.
• Support quality system improvement initiatives and CAPA's.
• Responsible for the assessment of technical standards, labeling and technical file requirements.
• Responsible for the assessment of component and system level specifications relative to customer
needs and product performance specifications.
• Perform requirement flow down analysis on critical to quality product performance specifications
down to components and process.
• Apply Design for Reliability and Manufacturability tools and techniques.
• Support for multiple projects, balancing priorities, and resources to meet both project and
management expectations.
• Prepare reports required by the project or department management.
• Reliable, consistent, and punctual attendance is an essential function of the job
• Complies with company, quality, and safety standards, policies, and procedures.
• Other duties as assigned.
This is not a remote position.
An individual in this position must be able to successfully perform the essential duties and responsibilities
listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform
the essential functions of this position.
QUALIFICATIONS
• Bachelor's Degree required with 0 years of experience, or a combination of education and relevant
work experience
• Knowledge of quality assurance and regulatory compliance including Quality System Standards
and Regulations.
• Knowledge of product development processes and methods.
• Knowledge of systems engineering discipline, Technical Standards, Hazard Analysis and Failure
Mode and Effects Analysis (FMEA), Qualification, Test Method and Process Validation.
• Must be able to read, write and speak fluent English
• Knowledge in the application of risk management
• ASQ Certification preferred
WHAT WE OFFER
• Ability to work on cutting edge lifesaving products
• 401(k) retirement savings with a company match
• Training and career development
• Tuition assistance
• Health care and well-being programs including medical, dental, and vision
• Paid time off
• Sign-on and referral bonuses
• Employee appreciation events
• Employee recognition program
• Clean and well-lit production areas
WORKING ENVIRONMENT
Work is performed in an office environment. The noise level in the work environment is usually moderate.
The work environment characteristics described here are representative of those an individual encounters
while performing the essential functions of this position.
EEO STATEMENT
Cirtec Medical Corporation is an Equal Opportunity Minority/Female/Individuals with
Disabilities/Protected Veteran and Affirmative Action Employer
Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age,
race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or
disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies
fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified
individuals with disabilities and disabled veterans in the job application process.
This is not a remote position
ABOUT THE COMPANY
More than just another design shop or contract manufacturer, Cirtec offers a uniquely comprehensive range of vertically integrated capabilities. Cirtec specializes in complex, difficult to produce components and devices in today's most advanced product technologies including, neuromodulation, implantable drug delivery, cardiac rhythm management, ventricular assist and interventional devices and delivery systems. We have the capabilities needed to bring products to full production, including assembly, packaging and testing, and in-house sterilization.
Our employees have the expertise needed to design innovative devices, solve complex design challenges, and help bring our customers' devices to market. If you are interested in working in a fun, challenging, fast-paced environment with a company that is growing and providing leading edge technology, Cirtec is the company for you!
YOU ARE A PART OF:
The engineering team consisting of other engineers with diverse backgrounds and expertise. The Engineering team works in close collaboration with Operations, R&D, and Purchasing. You will be involved in the design, development, documentation and validation of new customer products, and modification of existing products including defining requirements, timelines, and deliverables with a focus on prototypes, process development, design verification, clinical builds, training production, and preparation for process validation and manufacturing transfer of products.
JOB SUMMARY
The Engineer, Quality Design & Development is responsible for providing support to product development
teams and sustaining manufacturing/operations teams. This individual will be expected to apply design
control principles and techniques for medical devices. As a member of one or more cross-functional teams,
this individual will ensure products are designed and developed in accordance with applicable regulatory
requirements, customer requirements, and company policy.
ESSENTIAL RESPONSIBILITIES
• Perform Design Quality Engineering activities throughout the design, development, and production of
medical devices to ensure compliance to company's Design Control procedures and regulatory
requirements (specifically FDA 21 CFR 820 and ISO 13485).
• Create, review and/or approve technical Design Control documentation to facilitate design, development,
and product verification testing of medical devices in collaboration with cross-functional engineering teams.
• Create and execute Quality Plans for Product Design and Development projects.
• Represent Quality Engineering in technical design and phase end reviews.
• Develop and perform Design of Experiments (DOE).
• Develop and validate test methods.
• Develop sampling plans and acceptance criteria for product testing and inspection methods using
appropriate statistical techniques.
• Lead and/or participate in risk management activities, develop Risk Management Plans and Reports,
perform Hazards Analysis and FMEAs (Failure Mode Effects Analysis) to evaluate and ensure product
safety and functionality.
• Conduct and/or support root cause investigations, develop and implement corrective and preventative
actions for quality system and product related nonconformances.
• Support quality system improvement initiatives and CAPA's.
• Responsible for the assessment of technical standards, labeling and technical file requirements.
• Responsible for the assessment of component and system level specifications relative to customer
needs and product performance specifications.
• Perform requirement flow down analysis on critical to quality product performance specifications
down to components and process.
• Apply Design for Reliability and Manufacturability tools and techniques.
• Support for multiple projects, balancing priorities, and resources to meet both project and
management expectations.
• Prepare reports required by the project or department management.
• Reliable, consistent, and punctual attendance is an essential function of the job
• Complies with company, quality, and safety standards, policies, and procedures.
• Other duties as assigned.
This is not a remote position.
An individual in this position must be able to successfully perform the essential duties and responsibilities
listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform
the essential functions of this position.
QUALIFICATIONS
• Bachelor's Degree required with 0 years of experience, or a combination of education and relevant
work experience
• Knowledge of quality assurance and regulatory compliance including Quality System Standards
and Regulations.
• Knowledge of product development processes and methods.
• Knowledge of systems engineering discipline, Technical Standards, Hazard Analysis and Failure
Mode and Effects Analysis (FMEA), Qualification, Test Method and Process Validation.
• Must be able to read, write and speak fluent English
• Knowledge in the application of risk management
• ASQ Certification preferred
WHAT WE OFFER
• Ability to work on cutting edge lifesaving products
• 401(k) retirement savings with a company match
• Training and career development
• Tuition assistance
• Health care and well-being programs including medical, dental, and vision
• Paid time off
• Sign-on and referral bonuses
• Employee appreciation events
• Employee recognition program
• Clean and well-lit production areas
WORKING ENVIRONMENT
Work is performed in an office environment. The noise level in the work environment is usually moderate.
The work environment characteristics described here are representative of those an individual encounters
while performing the essential functions of this position.
EEO STATEMENT
Cirtec Medical Corporation is an Equal Opportunity Minority/Female/Individuals with
Disabilities/Protected Veteran and Affirmative Action Employer
Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age,
race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or
disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies
fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified
individuals with disabilities and disabled veterans in the job application process.
