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Senior Engineer, Product Development- Patient Safety

Job Description

ESSENTIAL DUTIES and RESPONSIBILITIES:

  • Serves as project leader, technical leader, or team player for projects including new product development, line extensions, product improvements, cost savings and sustaining projects.
  • Provides technical support to Manufacturing team as needed.
  • Develops timelines and project plans with cross-functional input.
  • Provides a sound working knowledge of engineering principals, concepts and practices.
  • Knowledgeable on FDA and ISO Design Controls, Risk Management and Design Transfer and follows TIDI procedures in accordance with regulations.   Completes all necessary documentation.
  • Interfaces with customers (marketing, end user customers and OEM customers) to translate user needs into design requirements and validate designs.
  • Creates projects documents, protocols, drawings and documentation to applicable internal and external standards.
  • Engages outside design firms, testing labs and technical consultants.
  • Demonstrates and actively supports TIDI Products, LLC Mission, Vision, Values, Value Discipline and Behaviors
  • Performs other tasks, as required or directed.

CORE VALUES & GUIDING PRINCIPLES:

  • Understands internal and external customers
  • Assures a safe work environment
  • Encourages individual development
  • Demonstrates teamwork and flexibility/adaptability
  • Demonstrates honesty
  • Keeps our commitments
  • Thinks systemically and ensure constancy of purpose
  • Leads with humility and respects every individual
  • Focuses on process, embraces scientific thinking, flow and pull value, assures quality at the source and seeks perfection 

Job Requirements

QUALIFICATIONS:

Education/Specialized Knowledge

  • BS Engineering Degree, (Mechanical or Biomedical preferred)
  • At least 5 years’ experience as an engineer in a medical device company.
  • Experience with products produced through industrial sewing is a benfit.
  • Experience in medical device development under FDA 21 CFR 820.30 Design Controls, ISO 13485 and ISO 14971 Risk Management. 
  • Working knowledge of U.S. and international standards as applicable to medical device development.
  • Minimum intermediate proficiency with AutoCad and Solidworks design software. 
  • Intermediate proficiency with Microsoft Outlook, Word, Excel, PowerPoint and Project.

Experience/Skills/Abilities and/or Training

  • Demonstrated engineering, analytical and technical skills
  • Demonstrated effective communication
  • Successful team player; demonstrated successful interpersonal and influence management skills
  • Track record of successfully collaborating with multiple functions and teams to drive successful project outcomes
  • Demonstrated project management skills.
  • Ability to travel up to 15% of the time. 
  • Energetic, self-motivated and can work independently; demonstrated strong work ethic.

Job Snapshot

Location US-IL-Lake Forest
Employment Type Full-Time
Pay Type Year
Pay Rate N/A
Store Type Engineering & Aerospace
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Company Overview

TIDI Products, LLC

TIDI exists to support caregivers and protect patients.​ ​TIDI has a history of providing forward-looking solutions to healthcare professionals—solutions that help reduce the risk of contamination and deliver the highest-quality patient care. ​ ​ Each day, caregivers turn to TIDI for a supply of user-friendly, compliance-enhancing, and risk-reducing solutions.​ The TIDI portfolio of brands includes Posey®, TIDIShield®, ​ C-Armor®, Grip-Lok®, Sterile-Z®, and Zero-Gravity®. ​ Learn More

Contact Information

US-IL-Lake Forest
Snapshot
TIDI Products, LLC
Company:
US-IL-Lake Forest
Location:
Full-Time
Employment Type:
Year
Pay Type:
N/A
Pay Rate:
Engineering & Aerospace
Store Type:

Job Description

ESSENTIAL DUTIES and RESPONSIBILITIES:

  • Serves as project leader, technical leader, or team player for projects including new product development, line extensions, product improvements, cost savings and sustaining projects.
  • Provides technical support to Manufacturing team as needed.
  • Develops timelines and project plans with cross-functional input.
  • Provides a sound working knowledge of engineering principals, concepts and practices.
  • Knowledgeable on FDA and ISO Design Controls, Risk Management and Design Transfer and follows TIDI procedures in accordance with regulations.   Completes all necessary documentation.
  • Interfaces with customers (marketing, end user customers and OEM customers) to translate user needs into design requirements and validate designs.
  • Creates projects documents, protocols, drawings and documentation to applicable internal and external standards.
  • Engages outside design firms, testing labs and technical consultants.
  • Demonstrates and actively supports TIDI Products, LLC Mission, Vision, Values, Value Discipline and Behaviors
  • Performs other tasks, as required or directed.

CORE VALUES & GUIDING PRINCIPLES:

  • Understands internal and external customers
  • Assures a safe work environment
  • Encourages individual development
  • Demonstrates teamwork and flexibility/adaptability
  • Demonstrates honesty
  • Keeps our commitments
  • Thinks systemically and ensure constancy of purpose
  • Leads with humility and respects every individual
  • Focuses on process, embraces scientific thinking, flow and pull value, assures quality at the source and seeks perfection 

Job Requirements

QUALIFICATIONS:

Education/Specialized Knowledge

  • BS Engineering Degree, (Mechanical or Biomedical preferred)
  • At least 5 years’ experience as an engineer in a medical device company.
  • Experience with products produced through industrial sewing is a benfit.
  • Experience in medical device development under FDA 21 CFR 820.30 Design Controls, ISO 13485 and ISO 14971 Risk Management. 
  • Working knowledge of U.S. and international standards as applicable to medical device development.
  • Minimum intermediate proficiency with AutoCad and Solidworks design software. 
  • Intermediate proficiency with Microsoft Outlook, Word, Excel, PowerPoint and Project.

Experience/Skills/Abilities and/or Training

  • Demonstrated engineering, analytical and technical skills
  • Demonstrated effective communication
  • Successful team player; demonstrated successful interpersonal and influence management skills
  • Track record of successfully collaborating with multiple functions and teams to drive successful project outcomes
  • Demonstrated project management skills.
  • Ability to travel up to 15% of the time. 
  • Energetic, self-motivated and can work independently; demonstrated strong work ethic.
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Senior Engineer, Product Development- Patient Safety Apply now