JOB REQUIREMENTS: About us: For over three decades, Cirtec Medical has
been a leading provider of manufacturing solutions for complex Class II
and III medical devices. We specialize in providing comprehensive
services from design and development to manufacturing and finished
device assembly. Our expertise spans active implants and
neuromodulation, interventional cardiology, structural heart, minimally
invasive surgical systems, smart orthopedics, and precision components.
Our dedicated teams prioritize growth, innovation, and collaboration. We
actively seek opportunities for improvement to enhance our support for
clients. If you embrace a growth mindset and thrive on challenge, you
may be a perfect fit for our team! Position Summary: The Process
Development Engineer I is primarily responsible for a functional project
engineering group within the department, consisting of multiple
engineering disciplines. They are 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. Key
Responsibilities: Attends and arranges project meetings to discuss
current and future design and development initiatives Track and
communicate issues, status on assigned action items that would affect
timelines and budget Can have responsibility for any of the following
project inputs: Feasibility builds, documentation, and testing Equipment
selection Process development and documentation Device Verification
samples and testing Operator training Process Failure Mode Effects
Analysis Clinical builds Process Validation May have involvement in the
design, development, and validation requirements of projects, including:
Product design and specification creation, including mechanical and
electrical components, assemblies, and packaging Materials sourcing and
device prototyping Design verification and validation activities,
including data for regulatory submission Manufacturing transfer and
support of existing product lines as applicable Complies with company,
quality, and safety standards, policies, and procedures Other duties as
assigned. Must Have: 4-year Bachelor\'s Degree in Engineering field\...
For full info follow application link. Cirtec Medical Corporation
considers everyone 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 its related companies fully endorse equal opportunity. Cirtec
Medical provides reasonable accommodation for qualified individuals with
disabilities and disabled veterans in the job application process.
\*\*\*\*\* APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/...B408B
been a leading provider of manufacturing solutions for complex Class II
and III medical devices. We specialize in providing comprehensive
services from design and development to manufacturing and finished
device assembly. Our expertise spans active implants and
neuromodulation, interventional cardiology, structural heart, minimally
invasive surgical systems, smart orthopedics, and precision components.
Our dedicated teams prioritize growth, innovation, and collaboration. We
actively seek opportunities for improvement to enhance our support for
clients. If you embrace a growth mindset and thrive on challenge, you
may be a perfect fit for our team! Position Summary: The Process
Development Engineer I is primarily responsible for a functional project
engineering group within the department, consisting of multiple
engineering disciplines. They are 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. Key
Responsibilities: Attends and arranges project meetings to discuss
current and future design and development initiatives Track and
communicate issues, status on assigned action items that would affect
timelines and budget Can have responsibility for any of the following
project inputs: Feasibility builds, documentation, and testing Equipment
selection Process development and documentation Device Verification
samples and testing Operator training Process Failure Mode Effects
Analysis Clinical builds Process Validation May have involvement in the
design, development, and validation requirements of projects, including:
Product design and specification creation, including mechanical and
electrical components, assemblies, and packaging Materials sourcing and
device prototyping Design verification and validation activities,
including data for regulatory submission Manufacturing transfer and
support of existing product lines as applicable Complies with company,
quality, and safety standards, policies, and procedures Other duties as
assigned. Must Have: 4-year Bachelor\'s Degree in Engineering field\...
For full info follow application link. Cirtec Medical Corporation
considers everyone 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 its related companies fully endorse equal opportunity. Cirtec
Medical provides reasonable accommodation for qualified individuals with
disabilities and disabled veterans in the job application process.
\*\*\*\*\* APPLICATION INSTRUCTIONS: Apply Online:
ipc.us/t/...B408B
Job ID: 479531212
Originally Posted on: 6/3/2025