Xeridiem Medical Devices Jobs Hiring Now
Xeridiem Medical Devices is hiring for 6 open roles on Migrate Mate as of July 16, 2026, concentrated in engineering (Non-Software) and manufacturing operations. Migrate Mate updates Xeridiem Medical Devices's live openings daily. Xeridiem Medical Devices is a medical device manufacturer that develops and produces minimally invasive catheter-based and single-use medical products.
Find Xeridiem Medical Devices JobsOverview
Xeridiem Medical Devices hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 6
- Top team
- Engineering (Non-Software)
- Seniority
- Across all levels
- Work type
- 0% remote or hybrid
- Top location
- Tucson
Open Roles at Xeridiem Medical Devices
Showing 6 of 6+ Xeridiem Medical Devices jobs
JOB PURPOSE:
Responsible for the design, development, procurement, and support of silicone processing equipment and tooling (including molding, extrusion, and related technologies). This role plans, designs, and coordinates the manufacture of tools and equipment that meet product and process specifications. Works closely with mechanical, product, and process engineering teams to transition equipment from concept through validation to a qualified production process.
ESSENTIAL DUTIES:
- Coordinate with cross-functional team members as needed during tooling and equipment qualification, sampling and final part approval
- Troubleshoot issues with production tooling and equipment, coordinate and execute repair activity as needed during development and modification phases
- Support production through ongoing maintenance and continuous improvement of tooling
- Perform minor tooling repairs utilizing onsite machine shop capabilities
- Provide manufacturing process development support for new and existing tooling
- Identify, evaluate, and develop external tooling and equipment suppliers as needed
- Lead and coordinate mold design reviews with tool vendors
- Manage tooling and equipment projects, including mold builds, validation, and largeequipment (e.g. presses, extruders)
- Coordinate implementation of cost effective tool design changes
- Support DFM/FMEA activities internally and with customers and suppliers
- Provide status reports to management and customers as needed
- Provide support to project teams as needed
- Partner cross-functionally to ensure timely project completion
- Communicates with customers and suppliers as needed
- Performs a variety of complex tasks using experience and judgment
- May lead and direct the work of others in various projects and assignments
- Upholds SPG and DuPont vision and core values
- Perform other duties as assigned
QUALIFICATIONS (Education/Experience/Knowledge, Skills & Abilities)
Required:
- Applicable Bachelor’s degree and/or equivalent experience in a related field
- Ability to design tooling and moderately complex silicone parts
- Proficient with SolidWorks
- Proficient in the use of Microsoft Office applications (Work, Excel, Outlook)
- Well organized, enthusiastic, high energy, strong work ethic
- Self-confident and comfortable with ambiguity. Relies on experience to make expert recommendations
- Working knowledge of quality improvement, lean manufacturing methods, statistical process controls, and process capability
- Proven track record of developing tooling and equipment for production of high quality, low cost, silicone parts.
- Medical device background
- Understands Lean manufacturing
- Has knowledge of commonly-used concepts, practices, and procedures within field
- Ability to problem solve identify errors and deficiencies and perform research independently
- Ability to apply knowledge to their job function using pre-established guidelines and instructions
- Accuracy, attention to detail, and thoroughness
- Proficient computer skills
- Proficient communications skills
- A wide degree of creativity and latitude
- Ability to comprehend and comply with company safety and quality standards
- Ability to follow oral and written instructions
- Responsible for understanding and complying with all SPG and Dupont safety policies and procedures.
Preferred:
- Participating member in a professional organization with engineering relevance (for example, ASME, SME, IIE, ISO, ASTM)
- Machining experience Minimum 10 years of hands-on experience involving specification, procurement, debug, and qualification of tooling and equipment for silicone processing (mill, extrude, mold, bond)
- Experience in manufacturing or with Medical Devices especially silicone processing
- Experience with Lean Manufacturing
WORKING CONDITIONS:
Works under general supervision. Requires light physical activity performing non-strenuous daily activities. About 40% of time will require standing and walking on the Production floor, where wearing of protective clothing might be necessary. About 60% of time will be spent working at desk and/or computer.
JOB PURPOSE:
Responsible for the design, development, procurement, and support of silicone processing equipment and tooling (including molding, extrusion, and related technologies). This role plans, designs, and coordinates the manufacture of tools and equipment that meet product and process specifications. Works closely with mechanical, product, and process engineering teams to transition equipment from concept through validation to a qualified production process.
ESSENTIAL DUTIES:
- Coordinate with cross-functional team members as needed during tooling and equipment qualification, sampling and final part approval
- Troubleshoot issues with production tooling and equipment, coordinate and execute repair activity as needed during development and modification phases
- Support production through ongoing maintenance and continuous improvement of tooling
- Perform minor tooling repairs utilizing onsite machine shop capabilities
- Provide manufacturing process development support for new and existing tooling
- Identify, evaluate, and develop external tooling and equipment suppliers as needed
- Lead and coordinate mold design reviews with tool vendors
- Manage tooling and equipment projects, including mold builds, validation, and largeequipment (e.g. presses, extruders)
- Coordinate implementation of cost effective tool design changes
- Support DFM/FMEA activities internally and with customers and suppliers
- Provide status reports to management and customers as needed
- Provide support to project teams as needed
- Partner cross-functionally to ensure timely project completion
- Communicates with customers and suppliers as needed
- Performs a variety of complex tasks using experience and judgment
- May lead and direct the work of others in various projects and assignments
- Upholds SPG and DuPont vision and core values
- Perform other duties as assigned
QUALIFICATIONS (Education/Experience/Knowledge, Skills & Abilities)
Required:
- Applicable Bachelor’s degree and/or equivalent experience in a related field
- Ability to design tooling and moderately complex silicone parts
- Proficient with SolidWorks
- Proficient in the use of Microsoft Office applications (Work, Excel, Outlook)
- Well organized, enthusiastic, high energy, strong work ethic
- Self-confident and comfortable with ambiguity. Relies on experience to make expert recommendations
- Working knowledge of quality improvement, lean manufacturing methods, statistical process controls, and process capability
- Proven track record of developing tooling and equipment for production of high quality, low cost, silicone parts.
- Medical device background
- Understands Lean manufacturing
- Has knowledge of commonly-used concepts, practices, and procedures within field
- Ability to problem solve identify errors and deficiencies and perform research independently
- Ability to apply knowledge to their job function using pre-established guidelines and instructions
- Accuracy, attention to detail, and thoroughness
- Proficient computer skills
- Proficient communications skills
- A wide degree of creativity and latitude
- Ability to comprehend and comply with company safety and quality standards
- Ability to follow oral and written instructions
- Responsible for understanding and complying with all SPG and Dupont safety policies and procedures.
Preferred:
- Participating member in a professional organization with engineering relevance (for example, ASME, SME, IIE, ISO, ASTM)
- Machining experience Minimum 10 years of hands-on experience involving specification, procurement, debug, and qualification of tooling and equipment for silicone processing (mill, extrude, mold, bond)
- Experience in manufacturing or with Medical Devices especially silicone processing
- Experience with Lean Manufacturing
WORKING CONDITIONS:
Works under general supervision. Requires light physical activity performing non-strenuous daily activities. About 40% of time will require standing and walking on the Production floor, where wearing of protective clothing might be necessary. About 60% of time will be spent working at desk and/or computer.
Job Roles at Xeridiem Medical Devices
Working at Xeridiem Medical Devices
Xeridiem Medical Devices's 6 open roles are across all levels, and about 0% are remote or hybrid. The most active teams are engineering (Non-Software), manufacturing operations, and content marketing. Xeridiem Medical Devices is a medical device manufacturer specializing in catheter-based and single-use products, with roles spanning engineering, quality, manufacturing operations, and environmental health and safety. Most Xeridiem Medical Devices roles are based in Tucson.
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Browse jobs by roleXeridiem Medical Devices Jobs: Frequently Asked Questions
How many jobs is Xeridiem Medical Devices hiring for right now?
Xeridiem Medical Devices is hiring for 6 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in engineering (Non-Software) and manufacturing operations. Open positions span engineering disciplines, manufacturing and production, quality assurance, and environmental health and safety. Migrate Mate pulls the latest postings directly so the count reflects what Xeridiem Medical Devices is actively filling.
What kinds of roles does Xeridiem Medical Devices hire for?
The most active teams are engineering (Non-Software), manufacturing operations, and content marketing. Xeridiem Medical Devices regularly hires across product development and tooling engineering, quality engineering, extrusion and manufacturing technician roles, and environmental health and safety positions. Most postings are across all levels, covering both hands-on production roles and specialized technical functions within a medical device manufacturing environment.
Are Xeridiem Medical Devices jobs remote or in-person?
Mostly on-site. About 0% of Xeridiem Medical Devices's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Tucson. Each Xeridiem Medical Devices listing shows its work location so you can filter before applying.
How do I apply to a job at Xeridiem Medical Devices?
Find a Xeridiem Medical Devices role on Migrate Mate, then follow the listing through to Xeridiem Medical Devices's own careers page to submit your application. Xeridiem Medical Devices manages its own hiring process, including screening, interviews, and offers. Migrate Mate keeps the listings current so you can confirm a role is still open before applying directly.
Does Xeridiem Medical Devices hire entry-level?
Most of Xeridiem Medical Devices's open roles on Migrate Mate are across all levels as of July 16, 2026. Check individual Xeridiem Medical Devices listings for stated experience requirements.
Where is Xeridiem Medical Devices hiring?
Most Xeridiem Medical Devices roles are based in Tucson, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.