What are the responsibilities and job description for the Sr Quality Engineer position at Artech L.L.C.?
Job Title: Sr Quality Engineer
Job ID: 15068
Location: 200 Client Dr Bldg 2, Lafayette, CO 80026 -Hybrid (3 days on site)
Duration: 24 Months
Pay Rate: $50-55/hr on W2
Job Description
Top Skills:
Product Part Approval Process Experience
Advanced Understanding of IQ, OQ, PQ
Molding Experience
Understanding of GD&T
Experience using statistical techniques like process capability
Education Required: Bachelor’s degree in engineering
Years’ Experience Required: Minimum of 4 years of relevant experience
Will the contractor be working 40 hours a week? If not, weekly estimate? 40 hours per week
Does this position require the candidate to be onsite or remote, if hybrid what does the onsite vs remote schedule look like? Hybrid, 3 days on site minimum
What is your timeline for scheduling interviews? ASAP
What product line will this person support? LigaSureTM and SonicisionTM products under Advanced Surgical Technologies
Sr. Supplier Quality Engineer
Careers That Change Lives
Help streamline and speed our time to market and build quality in at every step. You will be a member of the Released Product Engineering team that supports the design, development, and maintenance of innovative, new medical device products, as well as commercially released products within the Advanced Surgical Technologies business. You can apply advanced technical concepts to complex problems throughout the product life cycle.
In this role, you will work as part of a team, providing technical support on New Product Development and Sustaining Project Initiatives, ensuring medical devices are designed with the utmost regards to safety, reliability and quality. You will be responsible for reviewing supplier documentation including First Article Inspection Reports and OQ/PQ documentation and assisting with new component supplier qualifications with help from the Released Product Engineering team.
A Day In The Life
Ensures that suppliers deliver quality parts, materials, and services.
Qualifies suppliers according to company standards
Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur.
Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation.
Provides technical guidance and quality compliance for Supplier Quality engagement throughout the lifecycle on newly qualified parts and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements.
Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy and Control Plans for new components.
Must Haves
Bachelor’s degree and a minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years of relevant experience.
Product Part Approval Process Experience
Understanding of IQ, OQ, PQ
Molding Experience
Understanding of GD&T
Nice To Have
Degree in Engineering or Scientific discipline
CAD Experience
Detail-oriented with strong commitment to quality and to the workplace.
Excellent analytical, organizational, and communication skills. Strong ability to work with multidisciplinary and global teams.
High tolerance for change, and ability to multi-task continuously.
Strong negotiation, conflict management, and influence management skills.
Experience in the medical device industry.
About Client
Together, we can change healthcare worldwide. At Client, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Day in the Life section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Thank You
Devyansh Sharma
Associate Recruiter
Job ID: 15068
Location: 200 Client Dr Bldg 2, Lafayette, CO 80026 -Hybrid (3 days on site)
Duration: 24 Months
Pay Rate: $50-55/hr on W2
Job Description
Top Skills:
Product Part Approval Process Experience
Advanced Understanding of IQ, OQ, PQ
Molding Experience
Understanding of GD&T
Experience using statistical techniques like process capability
Education Required: Bachelor’s degree in engineering
Years’ Experience Required: Minimum of 4 years of relevant experience
Will the contractor be working 40 hours a week? If not, weekly estimate? 40 hours per week
Does this position require the candidate to be onsite or remote, if hybrid what does the onsite vs remote schedule look like? Hybrid, 3 days on site minimum
What is your timeline for scheduling interviews? ASAP
What product line will this person support? LigaSureTM and SonicisionTM products under Advanced Surgical Technologies
Sr. Supplier Quality Engineer
Careers That Change Lives
Help streamline and speed our time to market and build quality in at every step. You will be a member of the Released Product Engineering team that supports the design, development, and maintenance of innovative, new medical device products, as well as commercially released products within the Advanced Surgical Technologies business. You can apply advanced technical concepts to complex problems throughout the product life cycle.
In this role, you will work as part of a team, providing technical support on New Product Development and Sustaining Project Initiatives, ensuring medical devices are designed with the utmost regards to safety, reliability and quality. You will be responsible for reviewing supplier documentation including First Article Inspection Reports and OQ/PQ documentation and assisting with new component supplier qualifications with help from the Released Product Engineering team.
A Day In The Life
Ensures that suppliers deliver quality parts, materials, and services.
Qualifies suppliers according to company standards
Monitors parts from acquisition through the manufacturing cycle and communicates and resolves supplier-related problems as they occur.
Evaluates suppliers' internal functions to assess their overall performance and provides feedback in assessment of their operation.
Provides technical guidance and quality compliance for Supplier Quality engagement throughout the lifecycle on newly qualified parts and implementing strategies for driving product quality and continuous improvement, ensuring purchased products and components are manufactured and qualified in accordance to applicable industry standards, regulatory requirements, and customer requirements.
Collaborates with Component Engineers to develop and deliver the Product Acceptance Sampling Strategy and Control Plans for new components.
Must Haves
Bachelor’s degree and a minimum of 4 years of relevant experience, or advanced degree with a minimum of 2 years of relevant experience.
Product Part Approval Process Experience
Understanding of IQ, OQ, PQ
Molding Experience
Understanding of GD&T
Nice To Have
Degree in Engineering or Scientific discipline
CAD Experience
Detail-oriented with strong commitment to quality and to the workplace.
Excellent analytical, organizational, and communication skills. Strong ability to work with multidisciplinary and global teams.
High tolerance for change, and ability to multi-task continuously.
Strong negotiation, conflict management, and influence management skills.
Experience in the medical device industry.
About Client
Together, we can change healthcare worldwide. At Client, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. It is what makes this an exciting and rewarding place to be.
We want to accelerate and advance our ability to create meaningful innovations - but we will only succeed with the right people on our team. Let’s work together to address universal healthcare needs and improve patients’ lives. Help us shape the future.
Physical Job Requirements
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Day in the Life section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Thank You
Devyansh Sharma
Associate Recruiter
Salary : $50 - $55
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