Lead Engineer at Katalyst Healthcares Life Sciences
Sandy, Utah, USA -
Full Time


Start Date

Immediate

Expiry Date

12 Nov, 25

Salary

0.0

Posted On

12 Aug, 25

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Program Management, Design, Higher Education

Industry

Mechanical or Industrial Engineering

Description

JOB DESCRIPTION:

Onsite Engineer plans, leads, reviews and front-ends Design Verification, Sustaining Engineering and New Product Development projects as a technical contributor cum project leader and engages in all aspects of product development.

Responsibilities:

  • Leads the Design Verification, Sustaining Engineering & New Product Development projects and applies the best engineering practices and tools.
  • Demonstrates good project management, contributes on projects as the R&D member, carrying out assigned responsibilities in a timely, diligent, safe and professional manner.
  • Develops and maintains good rapport with business leaders, other internal functions, technical consultants, outside vendors, and other stakeholders to accomplish project objectives and be a strong team-player.
  • Reviews the deliverables to ensure completeness, accuracy and appropriateness of the design output / test executed and ensure its compliance to Good Documentation Practices.
  • Provides training to the team on GDP/GLP, IQ/OQ process, Calibration & Preventive maintenance activities and ensures the quality of deliverables.
  • Involves in the review / creation of DV Protocols and provides valuable inputs in terms of test equipment selection, capability / accuracy, sample size optimization, acceptance criteria definition, etc.
  • Conducts Weekly Status Review Meeting with stakeholders, shares the progress of various projects supported / led, keeps a track on the self-utilization.
  • Seeks for continuous improvement through value propositions (e.g. test method optimization) by identification of possible opportunities for time reduction / cost reduction / quality improvement.
  • Promptly follows-up with stakeholders for review / approval / signatures of project artifacts (including Memos, MSA, DV Protocol & Reports, IQ/OQ Protocols & Reports etc).
  • Quality System accountability: Maintains all relevant Protocols, Procedures, Reports and Records to ensure strict compliance of R&D functional operation to meet the Quality System requirements.
  • Provides cross-functional coordination based on project needs.
  • Supports the organization’s intellectual property strategy by documenting data and independent, unique and patentable ideas that result from experimentations.
  • Performs any other tasks (like Sustaining Engineering / New Product Development activities), as assigned.

Requirements:

  • Bachelor’s or higher education in Mechanical Engineering or related engineering / technology streams (Mechatronics / Polymer science / BioMedical / Plastics, etc…).
  • 5–7 years of relevant experience in product development and design.
  • 2–3 years of experience specifically in medical devices/products.
  • Proven track record in leading cross-functional teams through QMS and regulatory product development processes.
  • Demonstrated success in project or program management.
  • Strong communication and leadership capabilities.
  • Ability to influence stakeholders and work across functions.
  • Experience managing technical projects and cross-functional teams.
  • Familiarity with product development and compliance processes.
Responsibilities
  • Leads the Design Verification, Sustaining Engineering & New Product Development projects and applies the best engineering practices and tools.
  • Demonstrates good project management, contributes on projects as the R&D member, carrying out assigned responsibilities in a timely, diligent, safe and professional manner.
  • Develops and maintains good rapport with business leaders, other internal functions, technical consultants, outside vendors, and other stakeholders to accomplish project objectives and be a strong team-player.
  • Reviews the deliverables to ensure completeness, accuracy and appropriateness of the design output / test executed and ensure its compliance to Good Documentation Practices.
  • Provides training to the team on GDP/GLP, IQ/OQ process, Calibration & Preventive maintenance activities and ensures the quality of deliverables.
  • Involves in the review / creation of DV Protocols and provides valuable inputs in terms of test equipment selection, capability / accuracy, sample size optimization, acceptance criteria definition, etc.
  • Conducts Weekly Status Review Meeting with stakeholders, shares the progress of various projects supported / led, keeps a track on the self-utilization.
  • Seeks for continuous improvement through value propositions (e.g. test method optimization) by identification of possible opportunities for time reduction / cost reduction / quality improvement.
  • Promptly follows-up with stakeholders for review / approval / signatures of project artifacts (including Memos, MSA, DV Protocol & Reports, IQ/OQ Protocols & Reports etc).
  • Quality System accountability: Maintains all relevant Protocols, Procedures, Reports and Records to ensure strict compliance of R&D functional operation to meet the Quality System requirements.
  • Provides cross-functional coordination based on project needs.
  • Supports the organization’s intellectual property strategy by documenting data and independent, unique and patentable ideas that result from experimentations.
  • Performs any other tasks (like Sustaining Engineering / New Product Development activities), as assigned
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