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Open nowPosted 4 hours agoWe saw it 112 min after it went up

Principal Engineer

Inteldot25 open roles

Where
New Albany, Ohio, United States
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Your applicationOpen nowPrincipal EngineerInteldot · New Albany, Ohio, United States

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The clock on this job

Early applications get read.

12.4% of postings close within 7 days. Measured by our own scanner across the market. Inteldot postings stay open a median of 8 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.4%7 days
  4. 20.0%14 days
  5. 35.5%30 days
  6. 58.6%60 days
This job: posted 4 hours ago

Inteldot median: 8 days open

The posting

Industry: Pharmaceutical / Biotechnology Location: On-site in Ohio, USA Employment Type: Project-Based / Contract

Position Summary

Inteldot is seeking an experienced Principal Engineer to work closely with team members to develop detailed engineering specifications, develop and support characterization testing, develop protocols and validation testing.

Key Responsibilities

  • Work cross-functionally with individuals and project teams in Operations, Engineering and Automation.
  • Create and assess product requirements to determine technical coverage and proper integration different subsystems.
  • Create and execute to project plans and schedules.
  • Develop, execute, and review architecture documents, design documents, specifications, development plans, characterization plan, verification and validation plans and other related process development documents for assigned projects.
  • Provide deep technical assistance for junior engineers.

Skills & Requirements

  • BS in Engineering with previous experience in a Pharma or medical device industry.
  • 10 years current experience with engineering processes and procedures.
  • Led projects from process development through PPQ approval process.
  • Strong background in engineering for combination products.
  • Experience with material & test specs generation, protocol & report writing, process & test development, prototyping, design verification, DOE/SPC process optimization & validation (IQ, OQ, PQ), FMEA.
  • Experience in drug/device combination product assembly and packaging.
  • Familiar with the following standards: Quality System Regulation 21CFR820, Risk Management ISO 14971, EU Medical Device requirements.
  • Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
  • Strong problem solving, risk assessment, and risk management skills.
  • Must be capable of working on multiple projects in a deadline driven environment.
  • Qualified candidates with strong Electrical Engineering, Mechanical Engineering, Systems/Software Engineering background
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