Senior Staff Engineer – Advanced Operations

Posted 12 Days Ago
Be an Early Applicant
Portage, MI, USA
In-Office
103K-171K Annually
Senior level
Healthtech
The Role
Leads process engineering for new product introductions, including design transfer, manufacturing process development, equipment selection and validation, risk assessments, control plans, inspection methods, testing, and production validation. Partners with engineering, quality, manufacturing, regulatory, R&D, marketing, and project management teams to support compliant product launches. Provides technical guidance and mentors engineers.
Summary Generated by Built In
Work Flexibility: Onsite

Stryker Medical’s Advanced Operations team plays a key role in bringing new products into manufacturing. As a Senior Staff Engineer, you will provide process engineering leadership during design transfer, equipment implementation, and process development activities, partnering across engineering, quality, manufacturing, and regulatory teams to support successful product launches in a regulated environment.


What You Will Do

  • Lead process engineering activities for new product introductions, ensuring manufacturing readiness and compliance with design transfer requirements.
  • Develop and implement manufacturing processes, methods, and controls that meet product quality, cost, and schedule objectives.
  • Create and support process risk assessments, control plans, manufacturing procedures, and production validation activities for new product launches.
  • Evaluate, select, procure, install, and validate manufacturing equipment and capital assets to support production requirements.
  • Analyze process and equipment performance through testing, data collection, measurement system analysis, and experimental studies to optimize manufacturing outcomes.
  • Develop inspection methods, test protocols, and manufacturing controls to ensure products meet defined specifications and regulatory requirements.
  • Provide technical guidance on manufacturing standards, design requirements, testing strategies, and regulatory expectations while mentoring engineers and project teams.
  • Partner with Research & Development, Quality, Manufacturing, Regulatory Affairs, Marketing, and Project Management teams to resolve technical challenges and achieve project milestones.

What You Will Need

Required Qualifications

  • Bachelor's Degree in Engineering or a related technical discipline.
  • Minimum 6 years of experience in process engineering, manufacturing engineering, advanced operations, or a related technical field.
  • Experience interpreting system drawings involving mechanical, electrical, and software interactions.

Preferred Qualifications

  • Experience in an FDA-regulated industry or other highly regulated manufacturing environment.
  • Experience reading and interpreting engineering drawings, including geometric dimensioning and tolerancing (GD&T).
  • Certification(s) in Project Management, LEAN, Six Sigma, Operational Excellence, and/or related.

  


$102,600 - $171,000 USD Annual


  


Travel Percentage: 20%

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability.

Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Skills Required

  • Bachelor's degree in Engineering or a related technical discipline
  • Minimum 6 years of experience in process engineering, manufacturing engineering, advanced operations, or a related technical field
  • Experience interpreting system drawings involving mechanical, electrical, and software interactions
  • Experience in an FDA-regulated industry or other highly regulated manufacturing environment
  • Experience reading and interpreting engineering drawings, including geometric dimensioning and tolerancing (GD&T)
  • Certifications in Project Management, LEAN, Six Sigma, Operational Excellence, or related areas

Inari Medical Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Inari Medical and has not been reviewed or approved by Inari Medical.

  • Fair & Transparent Compensation — Pay is considered competitive for many roles, with employees described as 'extremely happy' with total compensation including pay, stock, equity, and benefits. Feedback suggests above‑average salary levels across departments contribute to strong pay sentiment.
  • Healthcare Strength — Benefits include comprehensive medical, dental, and vision coverage, with 100% employer‑paid premiums for employees cited in multiple descriptions. Additional options like critical illness, accident, hospital indemnity, and wellness programs reinforce the healthcare offering.
  • Leave & Time Off Breadth — Time off is characterized by unlimited PTO, cited as a top benefit by employees. Paid holidays and flexible hours are also referenced, expanding the range of time‑off options.

Inari Medical Insights

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The Company
HQ: Irvine, CA
956 Employees

What We Do

Inari Medical, Inc. is a commercial-stage medical device company focused on developing products to treat and transform the lives of patients suffering from venous diseases.

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