Senior Process Engineer, Advanced Operations

Posted 2 Days Ago
Be an Early Applicant
2 Locations
In-Office
78K-130K Annually
Senior level
Healthtech
The Role
Develop and support new manufacturing processes and product introductions, ensuring quality, documentation, validation, GMP, and safety compliance. Select equipment and components, support capital acquisition and installation validation, analyze process capability, conduct PFMEA and MSA studies, create control plans and inspection documentation, review validation records, and train manufacturing personnel. The role also supports process transfers, launches, and continuous process reviews.
Summary Generated by Built In
Work Flexibility: Onsite

Stryker is one of the world’s leading medical technology companies and is dedicated to helping healthcare professionals perform their jobs more efficiently while enhancing patient care. The Company offers a diverse array of innovative medical technologies, including reconstructive, medical and surgical, and neurotechnology and spine products to help people lead more active and more satisfying lives. We are currently seeking a Senior Engineer, Process Development to join our OrthoTech Division. This is an onsite position in Portage, MI.

What you will do:

  • Provide engineering support for new product and process introductions, ensuring that all activities are completed and documented in accordance with the Stryker new product development procedures.

  • Ensure quality of process and product as defined in the appropriate operation and material specifications.

  • Select components and equipment based on analysis of specifications, reliability and regulatory requirements. Work with quality engineers to develop component specific testing and inspection protocols.

  • Lead/support capital acquisition activity from specifying equipment, contract negotiation, Installation and validation.

  • Analyze equipment to establish operating data, conduct experimental test and result analysis. Lead and/or participate in process review meetings.

  • Participate in Process Failure Mode and Effect Analysis, Control Plan, SOP and Production Part Approval Process generation associated with product transfers and launches.

  • Complete capability studies for in process inspection and generate subsequent Inspection documentation.   

  • Conduct MSA studies for new products and new processes.

  • Provide training for manufacturing team members.

  • Ensure adherence to GMP and safety procedures.

  • Review and approval of validation documentation.

What you need:

  • Bachelor’s degree in engineering required

  • 2+ years of applicable full-time work experience required

  • Working knowledge of PFMEA required

  • Excellent analytical skills, ability to plan, organize, and implement concurrent tasks required

  • Good knowledge of manufacturing processes, materials, product and process design required

  • Ability to read and interpret complex engineering drawings and understand geometrical dimensioning and tolerancing (GD&T) required

  • CAD experience

  


$77,700 - $129,500 USD Annual

  


Travel Percentage: 10%

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
  • 2+ years of applicable full-time work experience
  • Working knowledge of PFMEA
  • Excellent analytical skills
  • Ability to plan, organize, and implement concurrent tasks
  • Knowledge of manufacturing processes, materials, product design, and process design
  • Ability to read and interpret complex engineering drawings
  • Understanding of geometrical dimensioning and tolerancing (GD&T)
  • CAD experience

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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