Senior Supplier Quality Engineer

LivaNova

Omaha (NE)

Hybrid

USD 110,000 - 120,000

Full time

14 days+

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Benefits offered by this job

Health benefits – Medical, Dental, Vision

Retirement & Savings Plan (401K)

Employee Stock Purchase Plan

Flexible Work Schedules

Job summary

LivaNova is seeking a Quality Engineer to lead supplier evaluations and ensure compliance with industry standards. This role offers remote flexibility, with responsibilities including technical leadership on component teams and conducting audits to maintain quality adherence.

The ideal candidate will hold a Bachelor's Degree in Engineering and possess over 8 years in Quality or Manufacturing Engineering, especially within regulated environments. Competitive salary ranges from $110,000 to $120,000, complemented by a discretionary bonus and comprehensive benefits.

Qualifications

8+ years of Quality or Manufacturing Engineering experience.
Experience in a regulated industry, preferably medical devices.
Strong understanding of statistical process control and risk management.

Responsibilities

Lead supplier selection, evaluation, and approval processes.
Provide technical leadership on component development teams.
Ensure compliance with ISO 13485 and MDSAP requirements.
Audit supplier Quality Management Systems.
Support procurement initiatives for cost-saving efforts.

Skills

Quality engineering principles

Project management

Interpersonal skills

Problem resolution

Education

Bachelor's Degree in Engineering

Job description

As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new day and our Mission to create ingenious solutions that ignite patient turnarounds. Our relentless commitment to patients and strong legacy of innovation in healthcare are the foundation of our future. If you're looking for a new chance, a new beginning, a new trajectory, LivaNova is where your talent can truly thrive. Join our talented team members worldwide to become a pioneer of tomorrow—because at LivaNova, we don’t just treat conditions — we aspire to alter the course of lives.

Location & Travel

This position is available as a Remote opportunity OR as a hybrid role, based at our site in Clear Lake, TX (Southeast Houston area)
This position may require business travel up to 25% of the time.

Job Duties

Leads the supplier selection, evaluation and approval process by assessing manufacturing/ technology capabilities, supplier risk levels, Quality Management System compliance, etc.
Serves as a core team member on component development teams by providing technical leadership and direction. Responsible for supplier process qualification, verification and validation activities
Reviews supplier process changes for completeness, accuracy, and safety/effectiveness including the identification of all impacts and timely management of these changes to ensure continued supply of parts
Acts as business process owner for all supplier related nonconformance report (NCR) management system, including material review board (MRB) activities, monitoring the timeliness and effectiveness of the system and activities;
Carries out supplier Quality Management System (QMS) and process audits
Collaborates with suppliers on process manufacturing process improvement, process validation (TMV, IQ, OQ and PQ) and value enhancement opportunities.
Ensures ongoing compliance per ISO 13485 and MDSAP requirements
Collaborates with Purchasing and procurement functions to support business strategy initiatives including cost saving efforts, alternate sourcing, outsourced processes etc.
Provides quality criteria (risk assessment, acceptance criteria, sample size, parameter definition) for receiving inspection activities;
Ensures that procedures and processes are maintained and updated to be consistent with regulatory changes including the development of more efficient QMS processes and global QMS processes;
Compiles and presents quality data to management as requested and in management review;
Contributes to successful regulatory audits by coordinating back room / front room activities or serving as a subject matter expert;
Supports enterprise resource planning controls and develop systems to ensure that parts and services are provided by approved sources
Performs other duties as may be required by management.

Minimum Qualifications

A Bachelor's Degree in Engineering is required
8+ Years of Quality or Manufacturing Engineering
Experience working in a regulated environment industry such as a FDA medical device manufacturer preferred.
Understanding of basic quality engineering principles including, but not limited to: quality leadership, implementation, acceptance sampling, statistical process control, lean business systems and other continuous improvement techniques, and risk management.
Pragmatic and result‑oriented: capable to prioritize and plan activities with specific attention to understand expectations of internal personnel and external stakeholders.
Good team player: open and honest when communicating among peers and management. Resolves most issues with peers, but understands what issues are important to escalation to management.
Project management skills including the ability to drive cross‑functional internal and external teams to completion of projects within planned timeframes. Strong interpersonal skills.
Sustained record of performance during tenure in previous position as shown through consistency with which metrics in their areas of responsibility meet performance objectives as established in Management Review and a track record of implementing improvements.

Pay Transparency

A reasonable estimate of the annual base salary for this position is $110,000 - 120,000 plus discretionary annual bonus. Pay ranges may vary by location and are awarded based on experience.

Employee Benefits Include