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Manufacturing Engineer

Job in Austin, Travis County, Texas, 78716, USA
Listing for: Sunrise Systems, Inc.
Full Time position
Listed on 2025-12-27
Job specializations:
  • Engineering
    Manufacturing Engineer, Quality Engineering, Process Engineer, Validation Engineer
Salary/Wage Range or Industry Benchmark: 45 - 47 USD Hourly USD 45.00 47.00 HOUR
Job Description & How to Apply Below

Pay Range

Base pay range: $45.00/hr - $47.00/hr

Senior Recruiter pay details provided by Sunrise Systems, Inc.

Senior Recruiter – Manufacturing Engineer, Sr.

Job Title: Manufacturing Engineer, Sr

Location: Austin, TX

Duration: 6 Months

Position Type: W2 Contract

Description

At Client, we design and manufacture technology that takes the limits off living. Are you ready to apply your engineering expertise to work that truly makes a difference? Join our U.S. Orthopedics team as a Contract Senior Manufacturing Transfer Engineer and play a key role in ensuring our orthopedic products are manufactured and delivered with excellence. This is an exciting short‑term opportunity for an experienced engineer to lead complex site and manufacturing transfer projects that directly impact patient outcomes.

What

You’ll Do

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 client’s world‑class standards for quality, safety, and compliance.

Key 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.
What You’ll Need

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 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.
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