Aspensurgical

26 Aspensurgical Jobs Hiring Near You

Summary The Sr Design Engineer is responsible for Design medical devices to support the growth, cost profile, and business continuity of Aspen Surgical products while working in a collaborative team ...

Summary Join Aspen Surgical' s Commercial Sales Team as an Account Manager in the Acute Sales segment of the business. With a comprehensive portfolio of industry-trusted surgical essentials and ...

Summary Join Aspen Surgical' s Commercial Sales Team as an Account Manager in the Acute Sales segment of the business. With a comprehensive portfolio of industry-trusted surgical essentials and ...

Summary Join Aspen Surgical' s Commercial Sales Team as an Account Manager in the Acute Sales segment of the business. With a comprehensive portfolio of industry-trusted surgical essentials and ...

Quality Engineer (NY)

Jamaica, NY

$75K - $97K/yr

Summary The Quality Engineer supports a chemical mixing / medical device manufacturing operation, ensuring compliance with applicable quality system regulations while providing direct shop-floor ...

JOB SUMMARY: Responsible for adjusting production machinery, testing to correct faults, light mechanical repairs and carry out preventive maintenance. Responsible for the operation of the production ...

Summary This role is responsible for supporting and leading global packaging functions across sterile and non-sterile medical device products. The Senior Packaging Engineer will drive packaging ...

JOB SUMMARY: The Process Engineer supports maintenance and continuous improvement activities within the surgical blade's operation, focusing on optimizing machine output, reducing waste, and ensuring ...

Summary Join Aspen Surgical's Commercial Sales Team as a Region Director in the Acute Sales segment of the business. With a comprehensive portfolio of industry-trusted surgical essentials and ...

Operator

Jamaica, NY

$18.50 - $24.25/hr

In This Position, You Will Have the Opportunity To * Listen actively and takes direction from Supervisor regarding daily work priorities * Assemble, inspect, and package product per cell work ...

Summary Buyer will be responsible for managing procurement and supplier relationships for two sites, while supporting the Director of Strategic Sourcing in integrating legacy procurement processes ...

Summary The Supplier Quality Manager is a corporate-level quality leadership role responsible for developing, aligning and governing supplier quality processes across Aspen's global operations in a ...

New

Quality Technician (2nd Shift)

Caledonia, MI

$17.25 - $23.25/hr

In This Position, You Will Have the Opportunity to * Support validation and risk build activities with manufacturing and engineering group * Perform Customer Complaint Investigations, including ...

Shipping Clerk

Jamaica, NY

$17.25 - $20.50/hr

In This Position, You Will Have the Opportunity To * Accurately and efficiently picks, packs, and ships products, meeting all established productivity and quality goals in place for the current ...

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Posted 4 days ago


Job description

 

Summary

The Sr Design Engineer is responsible for Design medical devices to support the growth, cost profile, and business continuity of Aspen Surgical products while working in a collaborative team environment.

 

In This Position, You Will Have the Opportunity to:

  • Support design tasks associated with global revenue growth and margin improvement projects
  • Support organic growth functions of acquisitions and other business migrations
  • Support sustaining engineering functions of the organization to maintain business continuity

Medical Device Product Development

  • Execute medical device design history file activities to be compliant with applicable regulations
  • Conduct the development and evaluation of medical device designs which meet defined product requirements and that are optimized for safe clinical solutions, production, reliability, and overall cost effectiveness for the business
  • Provide technical assistance to various departments and individuals as necessary in the exploration of new opportunities
  • Evaluate proposed changes to existing products and complete deliverables required to implement the change through individual efforts or cross-functional teams
  • Ensure that product changes meet regulations as well as internal and external customer requirements
  • Troubleshoot and problem-solve efforts related to product design.
  • Conduct thorough engineering and data analysis.

Project Management

  • Responsible for project schedules, budgets, mitigating risks, and efficient solutioning of issues
  • Recommend and communicate project plans, track tasks, and manage time to meet project deadlines
  • Executive presence for communicating with leaders in a clear efficient manner

 

Global Collaboration

  • Work closely with the portfolio managers to understand clinical and commercial impacts.
  • Strong communication skills to convey design concepts to clinicians to obtain design direction
  • Work with manufacturing throughout the development phases to ensure that products are produced in a safe, efficacious, and quality manner while keeping within established time frames
  • Work with finance to develop product costing to understand impacts of material/design selections
  • Interface with vendors, manufacturing facilities, and various internal groups to resolve design and manufacturing issues of new and existing products
  • Provide peer mentoring and guidance to other engineers throughout the company

What You Need to Succeed in This Position

  • Bachelor of Science Degree in Engineering or closely related 4-year technical degree is required
  • 7+ years of medical device engineering experience preferred
  • PMP certification preferred
  • Regulated industry experience that includes, but not limited to, FDA 21CFR820.30, ISO 13485, ISO 14971, MDSAP and European MDD/MDR requirements.
  • Working knowledge with ISO 11607 regulations and transit testing to ASTM 4169 or similar testing standards
  • Experience with IEC 60601 (Medical Electrical Equipment Safety and Performance Requirements) and/or IEC 62304 (Medical Device Software Lifecycle Requirements) preferred.
  • Strong familiarity with the methods of Risk Management and Failure Mode Effects Analysis (FMEA)
  • Working knowledge of design history & technical file within an auditing environment.
  • Working knowledge of statistical analysis of data used to meet or define design criteria
  • Project management experience to effectively manage and complete multiple projects simultaneously
  • Involvement with invention disclosures or patents
  • Business case development for product costing as it pertains to design
  • Preferred experience using engineering programs such as SolidWorks, Minitab, TOPS, similar.
  • Teamwork, effective communication, and positive attitude required to fit & grow culture
  • Effectively handles global interactions and collaborations while managing cultural differences.
  • Models clinical safety and quality first mindset
  • Takes initiative and proactively mitigates risks
  • Continuous education focused to advance job knowledge in medical device design & development
  • Excellent computer skills including but not limited to Microsoft Office Suite
  • On site job located in Caledonia, MI with 15% expected travel