Summary written by USA Jobs 24 from Stryker's advert and our data on 16,857 current US jobs. How we check every job
At a glance
Stryker is hiring a Senior Engineer, Quality Process in Phoenix, AZ. It is a full-time role in Software & IT, asking for at least 2 years of experience, first listed on November 13. The advertised pay is $69,500–$110,900 a year. The description mentions Six Sigma, Statistics and Excel. Stryker has 99 other openings in the US, 2 of them in Phoenix, AZ. Across all employers on USA Jobs 24 there are 25 Software & IT openings in Phoenix, AZ today; the typical one asks for 5 years and advertises about $187,000 a year at the midpoint.
How the pay compares
Stryker advertises $69,500 to $110,900 a year, a midpoint of $90,200 a year. Where an offer lands in a range usually depends on experience and on the exact location. That is lower than about 94% of the 53 software & IT jobs in Arizona that publish a yearly rate on USA Jobs 24, where the typical midpoint is $151,000 a year. To see roughly what this leaves after federal and Arizona tax, try our take-home pay calculator.
Skills in this advert
How often each skill named in this advert appears across the 4,401 software & IT jobs we list today. Statistics is the most widely requested (5% of jobs), while Six Sigma is the least common (2%). Widely requested skills are what employers expect as a baseline; rarer ones show what is special about this job.
Paste your resume and this advert into our resume match tool to see which of these words your resume already covers.
Before you apply
- Check it is still open. We found this job on Stryker's Workday site on November 13 and checked it again November 13, 5:17 AM ET. When an employer takes a job down, we remove it at our next daily update.
- Check the location works for you. This role is based in Phoenix, AZ. If you would need to move, ask whether relocation help is offered.
- Match the experience. The advert asks for at least 2 years of experience. If you are a little short, a close match on the skills in the advert can still win an interview.
- Tailor your resume. Use the advert's own words, such as Six Sigma, Statistics and Excel, wherever they are true for you. Our resume guide shows how.
- Know your number. Decide the lowest offer you would accept before the first call. Our salary negotiation guide explains how to ask for more.
- Apply only through Stryker's own site. Our Apply button goes straight to Stryker's Workday page. If anyone contacts you about this job and asks for money, gift cards or bank details, stop and check it with our scam checker. Read how to spot a fake job offer.
About hiring at Stryker
Stryker has 100 openings on USA Jobs 24 today across 36 states. Most are in sales & BD (45), healthcare & pharma (11) and software & IT (10). The biggest locations are Denver, CO (6), Dallas, TX (6) and Portage, MI (4). 5% of them are remote, 21% are open to entry-level candidates and 26% show pay. We collect Stryker's jobs every day straight from its own careers system (Workday), never from job boards or agencies.
The employer's advert
This is Stryker's own description of the job, copied word for word from its careers site. We have not edited it.
Show the full advert from StrykerHide the advert689 words
Stryker is hiring a Senior Quality Engineer in Phoenix, Arizona, to support Sustainability Solutions! In this role, you will be responsible for analyzing and resolving production issues through collaboration with engineering and material procurement teams. Furthermore, you will perform monitoring of process data and analysis of trends, financial results, and customer feedback. You will exhibit a commitment to quality first culture, compliance, and continuous improvement through the implementation of projects which optimize production, inspection, and quality system processes.
What you will do
- Work closely with operations and the business functions to ensure quality performance of product and processes
- Collaborate cross-functionally with internal and external teams to resolve quality issues
- Manages internal and supplier-driven Non-Conformances (NCs), ensuring timely investigation and closure
- Owns Corrective and Preventive Actions (CAPAs) through root cause analysis to closure
- Disposition of non-conforming product through MRB, issuing NCs as appropriate
- Initiates and leads in the development and improvement of the manufacturing processes for existing and new products.
- Review and approval of change management activities, challenges change effectiveness and drives strong review.
- Interpret KPI trends, act as necessary, driving a continuous improvement process.
- Support the execution and analysis of manufacturing complaints and product field actions
- Provide QA support during internal and external audits
- Advocate of Human Factor practices, proficient in the science of Human Factor identification and mitigation.
- Proficient in risk management practices and concepts and applies knowledge to manufacturing operations and identify opportunities and weaknesses
- Lead and participate in the Lean philosophy – standardization and elimination of waste
- Understanding of Human Error Prevention and the application of those principles to the manufacturing environment.
- Support process/equipment validation, qualification, and Measurement System Analysis (MSA)
- Support with product holds and executing containment plans
- Manage supplier relationships, including but not limited to, coordinating communications, monitoring performance, managing in house and external nonconformities and ensuring timely delivery of quality materials and services.
What you need
- B.S. in engineering, or related discipline
- 2+ years as a Quality Engineer in a manufacturing environment.
Preferred
- Proficient in understanding of Med Device manufacturing processes, ISO 13485, GMP.
- Lean Six Sigma training is a distinct advantage.
- Excellent communication skills and attention to detail.
- Proficient understanding of engineering and quality principles, including Risk Management, CAPA, Audits, and Statistics
- High level knowledge/experience of Risk Based and statistical techniques, in particular process risk, statistical sampling plans, Process Capability, Gauge R&Rs.
- High level of PC skills. Must be proficient with Microsoft Word, Microsoft Excel and PowerPoint packages.
- Experience in interacting with regulatory agencies (FDA, MoH, TUV, etc.) desired.
- Strong knowledge of Quality Concepts (e.g. Risk Management, CAPA, Audits, Statistics).
- Confident representing Quality in cross-functional settings
- Self-starter able to manage multiple tasks in a fast-paced environment
- Willing to work as part of a multi-site team; some travel required
United States of America Pay Ranges:
- Puerto Rico: $69,500 - $110,900 USD Annual
- USN: $77,700 - $129,500 USD Annual
- US5: $81,600 - $136,000 USD Annual
- US10: $85,500 - $142,500 USD Annual
- US15: $89,400 - $148,900 USD Annual
- US20: $93,200 - $155,400 USD Annual
- US30: $101,000 - $168,400 USD Annual
USA Jobs 24 copied this listing from Stryker's official careers site on November 13, 2026 and checked it again November 13, 5:17 AM ET. Stryker will never ask you to pay to apply or to buy equipment with a check they send you. If anyone does, it is a scam.
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