Med Device Manufacturing Engineer II
Listed on 2026-07-09
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Quality Assurance - QA/QC
Production QC/QA
Job Title:
Manufacturing Engineer II
We are seeking a hands‑on Manufacturing Engineer to support a strategic two‑year equipment transfer and in sourcing initiative by relocating manufacturing equipment from another facility, bringing it online, and enabling the transition of externally supplied products to in‑house production.
Responsibilities- Lead and support commissioning, installation, and qualification of manufacturing equipment transferred from Costa Rica to the Warsaw facility.
- Perform equipment inspection, setup, and validation to ensure compliance with quality and regulatory standards.
- Execute and document equipment validation protocols (IQ/OQ/PQ).
- Troubleshoot and optimize machining and automated manufacturing equipment, including lathes and other production systems.
- Collaborate cross‑functionally with operations, quality, and validation teams to ensure timely production readiness.
- Support the in sourcing effort, enabling a smooth transition of product manufacturing from suppliers to internal operations.
- Maintain strong documentation practices aligned with medical device regulatory standards.
- Bachelor’s degree in Engineering (Mechanical, Manufacturing, or related field).
- 3–5 years of relevant experience in manufacturing engineering within the medical device industry.
- Experience with equipment commissioning, validation, and qualification (IQ/OQ/PQ).
- Hands‑on experience with machining equipment, lathes, and/or automated manufacturing systems.
- Strong understanding of quality standards and regulated manufacturing environments.
Skills & Qualifications
- Self‑starter with a proactive mentality and ability to work independently in a fast‑paced project environment.
- Strong communication and cross‑functional collaboration skills.
- Detail‑oriented with a proactive approach to problem‑solving.
- Comfortable in a hands‑on, shop‑floor‑focused role.
This role is based onsite with working hours from 8 am to 5 pm. The environment is fast‑paced and project‑focused, involving direct interaction with advanced manufacturing equipment and processes. The position offers visibility across engineering, operations, and quality teams within a leading medical device organization.
Job Type & LocationContract position based out of Warsaw, IN.
Pay and BenefitsPay range: $40.00–$48.00 per hour.
Benefits Summary- Medical, dental & vision
- Critical Illness, Accident, and Hospital
- 401(k) Retirement Plan – Pre‑tax and Roth post‑tax contributions available
- Life Insurance (Voluntary Life & AD&D for the employee and dependents)
- Short and long‑term disability
- Health Spending Account (HSA)
- Transportation benefits
- Employee Assistance Program
- Time Off/Leave (PTO, Vacation or Sick Leave)
Position anticipated to close on July 8, 2026.
Equal Opportunity EmployerActalent is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Reasonable AccommodationRequest a reasonable accommodation, such as modification or adjustment of the job application process or interviewing process due to a disability, by emailing actalentaccom
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