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Manufacturing Engineer

Job in Austin, Travis County, Texas, 78716, USA
Listing for: neteffects
Full Time position
Listed on 2025-12-27
Job specializations:
  • Engineering
    Quality Engineering, Manufacturing Engineer, Process Engineer
Salary/Wage Range or Industry Benchmark: 43 - 46 USD Hourly USD 43.00 46.00 HOUR
Job Description & How to Apply Below

Location
:
Austin, TX

Pay Rate
: $43.00 - $46.00/hr

Duration
: 6 months

Hours
: 8-5pm

Summary

As a member of the U.S. Orthopedics Operations Engineering team, you’ll lead the planning and execution of manufacturing transfers across our global network. You’ll coordinate technical readiness, validation activities, and process documentation to ensure smooth transitions between manufacturing sites—while maintaining world‑class standards for quality, safety, and compliance.

Responsibilities
  • Execute end‑to‑end manufacturing and site transfer projects, including planning, risk assessment, validation, and handover.
  • Coordinate all technical documentation, process flows, and equipment readiness activities at both sending and receiving sites.
  • Support process and equipment validation (IQ/OQ/PQ) and ensure compliance with FDA and ISO 13485 requirements.
  • Partner cross‑functionally with Quality, Regulatory, Supply Chain, Manufacturing, and R&D to ensure alignment and readiness.
  • Lead root cause analysis and technical problem‑solving throughout the transfer lifecycle.
  • Prepare and maintain project documentation, including validation protocols, reports, and change control packages.
  • Communicate project progress, risks, and mitigation strategies to stakeholders at all levels.
  • Capture and share lessons learned to continuously improve future transfer processes.

Success in this role requires technical expertise, attention to detail, and a collaborative mindset. You should be comfortable managing multiple priorities in a fast‑paced, regulated environment.

Required Qualifications
  • Bachelor’s degree in engineering, science, or related discipline.
  • Minimum of 4 years of experience in medical device manufacturing or other regulated industries.
  • Proven track record leading or supporting site or manufacturing transfers.
  • Or, proven track record of new product launches into existing sites.
  • Strong knowledge of process validation, change control, and manufacturing documentation.
  • Excellent problem‑solving, communication, and organizational skills.
  • Ability to work independently and drive results with minimal supervision.
Preferred Qualifications
  • Experience with orthopedic implants, instruments, or precision assembly.
  • Familiarity with lean manufacturing and Six Sigma methodologies.
  • Proficiency with ERP, PLM, or MES systems.
Benefits (employee contribution)
  • Health insurance
  • Health savings account
  • Dental insurance
  • Vision insurance
  • Flexible spending accounts
  • Life insurance
  • Retirement plan

All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. Rate of pay within the stated range will depend on the qualification of the applicant.

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