Spectranetics

Design Quality Engineer

Spectranetics$103K — $163K *
Healthcare
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Minimum 3+ years in FDA regulated medical device environments focusing on Design Assurance and Sustaining/Post Market Complaint investigations.
  • Proven knowledge in Risk Management (ISO 14971), FMEA/DFMEA, Design Verification/Validation, Root Cause analysis, and Defect Management.
  • Experience in implementing and supporting processes and tools for tracking/preventing product defects and ensuring design traceability.
  • Skilled in using Post Market Surveillance (PMS) insights and data analytics for continuous improvement in the product lifecycle.
  • Ability to share expertise on quality standards and regulatory requirements.
  • Bachelor's Degree in Quality, Engineering or a similar discipline.
  • Must meet minimum Physical, Cognitive, and Environmental job requirements.

Responsibilities

  • Ensure adherence to quality plans focused on sustaining and handling product complaints.
  • Contribute to design input processes and validation activities to meet design requirements.
  • Validate key design inputs, including usability, safety, and manufacturability.
  • Maintain updated Design History Files.
  • Provide input for Risk Management activities throughout the product lifecycle.
  • Conduct routine risk management updates.
  • Assess product quality performance and analyze post-market data for reports on efficacy and efficiency in design and realization processes.

Benefits

  • Comprehensive Philips Total Rewards benefits, including a generous PTO.
  • 401k with up to 7% company match.
  • HSA with company contribution.
  • Education reimbursement for professional development.
  • Employee stock purchase plan.
Full Job Description
Job Title
Design Quality Engineer

Job Description

The Design Quality Engineer is accountable for design quality, risk management, sustaining and complaint investigations for Philips Image Guided Therapy products.  

Your role:

  • Ensures that appropriate quality plans are followed with a focus on sustaining and product complaint investigations.
  • Provides input to design I/O process, design V&V activities, design transfer and product realization, and performance in the field to ensure that all design requirements are effectively met. 
  • Validates key design inputs: usability, reliability, performance, supportability, manufacturability, localizability, safety, security, privacy, serviceability, sustainability and costs
  • Maintain Desing history files updated.
  • Provides effective input for Risk Management activities, and of all design related activities during the product/system lifecycle
  • Perform routine risk management updates.
  • Performs technical assessment on product quality performance and post-market product quality analysis.
  • Performs post-market data analysis/statistics to report on product quality performance in the field and to the Business on the efficacy and efficiency of the design and product realization processes.  
  • Initiates field actions/CAPA when required.

You're the right fit if:

  • You have a minimum of 3+ years’ experience in FDA regulated medical device environments, with a focus on Design Assurance, Sustaining and Post Market Complaint investigations.
  • You have proven experience/knowledge in Risk Management (ISO 14971), FMEA/DFMEA, Design Verification/Validation, Root Cause analysis and Defect Management.
  • You have detailed experience in identifying, promoting, and supporting processes and design quality tools for use in tracking/preventing product defects, design traceability, and Design for Reliability.
  • You’re experienced in utilizing Post Market Surveillance (PMS) insights/data analytics to lead continuous improvement throughout all stages of the product lifecycle.
  • You’re able to share knowledge, insights regarding quality standards, and regulatory requirements.
  • You have a minimum of a Bachelor’s Degree (Required), in Quality, Engineering or similar disciplines.
  • You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this . 

How we work together:

We believe that we are better together than a part. For our Office-based teams, this means working in-person at least 3 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations. This is an Office role.

Philips Transparency Details:

  • The pay range for this position in Bedford, MA is $103,000 to $163,000.

The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.  

At Philips, it is not typical for an individual to be hired at or near the top end of the range for their role and compensation decisions are dependent upon the facts and circumstances of each case. 

In addition, other compensation, such as an annual incentive bonus, sales commission or long-term incentives may be offered.  Employees are eligible to participate in our comprehensive Philips Total Rewards benefits program, which includes a generous PTO, 401k (up to 7% match), HSA (with company contribution), stock purchase plan, education reimbursement and much more.  Details about our benefits can be found . 

Additional Information:

  • US work authorization is a precondition of employment. The company will not consider candidates who require sponsorship for a work-authorized visa, now or in the future.
  • Company relocation benefits WILL NOT be provided for this position.  For this position, you must reside in or within commuting distance to Bedford, MA
  • May require travel up to 10%.

This requisition is expected to stay active for 45 days but may close earlier if a successful candidate is selected or business necessity dictates.  Interested candidates are encouraged to apply as soon as possible to ensure consideration.

About Spectranetics

Spectranetics is a medical device company that develops, manufactures, and markets single-use medical devices used in minimally invasive procedures within the cardiovascular system. The company's products include laser atherectomy systems, thrombectomy systems, and lead management accessories. Spectranetics was founded in 1984 and is headquartered in Colorado Springs, Colorado. In 2017, the company was acquired by Royal Philips for $2.2 billion.
Learn more about Spectranetics
Size
900 employees
Industry
Founded
1980

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