Skip to content
CV Rocket
Get started
How it worksThe enginePricingBlogContactSign in

Open nowPosted 25 hours ago

Quality Assurance - Quality Engineer I

Viant77 open roles

Pay
$80,000 – $100,000 a year
Where
Orchard Park, NY 14127, USA
Get the CV for this job

From $25 per CV, paid once. No subscription.

Your applicationOpen nowQuality Assurance - Quality Engineer IViant · Orchard Park, NY 14127, USA

  1. YouYes, apply to this one.

  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on Viant's own form.

The reply lands in your private mailbox

3×more interviews than doing it yourself with ChatGPT.

The clock on this job

Early applications get read.

13.3% of postings close within 7 days. Measured by our own scanner across the market. Viant postings stay open a median of 20 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.6%3 days
  3. 13.3%7 days
  4. 21.3%14 days
  5. 35.7%30 days
  6. 59.1%60 days
This job: posted 25 hours ago

Viant median: 20 days open

The posting

Quality Engineer I

Why Join Us?

Are you passionate about quality, problem-solving, and making a meaningful impact? Join Viant and help bring innovative, life-changing medical technologies to patients around the world. As a Quality Engineer I, you will work alongside experienced professionals, gain exposure to cutting-edge manufacturing and quality systems, and play a key role in ensuring the safety and reliability of products that improve lives. At Viant, we are committed to your growth and success because We're In It For Life.

About the Company Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, we help bring innovative healthcare technologies to market efficiently and reliably.

About the Site Located in Orchard Park, New York, our facility supports the development and manufacture of innovative medical device technologies. Team members work in a collaborative environment focused on quality, continuous improvement, and delivering products that enhance patient lives.

About the Role This is an excellent opportunity for an early-career quality professional looking to expand their experience in the medical device industry. You will partner with cross-functional teams across Manufacturing, Engineering, and Quality while developing expertise in regulatory compliance, process validation, continuous improvement, and new product development. Every day offers opportunities to learn, contribute, and make a difference.

In This Role, You Will Have the Opportunity To:

Support the quality and compliance of innovative medical device products. Collaborate with manufacturing, engineering, and customer teams to solve complex challenges. Drive continuous improvement initiatives utilizing SPC, FMEA, DOE, and process validation tools. Participate in new product introductions and help bring new technologies to market. Develop your expertise in regulatory requirements, quality systems, and supplier quality. Lead investigations, corrective actions, and efforts that improve product quality and reliability.

Responsibilities

Maintain compliance with FDA Quality System Regulations and ISO 13485 requirements. Participate in internal audits, management reviews, and quality system activities. Support customer quality and regulatory inquiries. Develop and deliver training related to quality systems and quality control activities. Provide quality engineering support for new product development and product launches. Lead or support continuous improvement activities utilizing tools such as SPC, FMEA, DOE, and process validation. Develop inspection, testing, and evaluation methods to improve product quality and reliability. Perform measurement system analyses and support calibration programs. Lead investigations and disposition activities for nonconforming materials and quality issues. Support supplier qualification, audits, corrective actions, and ongoing supplier quality activities.

Job Requirements Education Bachelor's degree in Engineering, Quality, Manufacturing, or a related technical or scientific field, or equivalent combination of certification and experience. CQE certification is a plus. Experience Minimum 2 years of experience in the medical device industry or another regulated manufacturing environment. Minimum 2 years of experience supporting new product development and quality engineering activities. Experience with FDA regulations, ISO 13485, and quality management systems preferred. Knowledge & Skills

Knowledge of quality engineering principles and tools including SPC, FMEA, DOE, root cause analysis, and process validation. Proficiency with Microsoft Excel and statistical analysis software; Minitab experience preferred. Familiarity with supplier quality processes, audits, and corrective action systems. Experience with Lean Manufacturing or Six Sigma methodologies is a plus. Skills & Competencies Strong analytical and problem-solving skills. Excellent verbal and written communication abilities. Ability to manage multiple priorities in a fast-paced environment. Ability to work independently while collaborating effectively across departments.

Benefits Benefits effective day one of hire:

Medical, dental, and vision coverage 401(k) plan with company match Generous paid time off and paid holidays Low-cost nutrition and mental health visits Tuition reimbursement and career development programs Company-paid life insurance Access to individualized financial planning Pet insurance Employee discount programs Home ownership program

Compensation We offer market competitive compensation. Potential salary range for this role is $80,000 - $100,000 annually. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. Apply Today Ready to build a rewarding career while helping improve patient lives around the world? Join a team that values innovation, collaboration, and continuous growth. We look forward to learning how your talents can contribute to Viant's mission. Apply today!

From $25, paid onceGet the CV for this job

What happens when you press

One press. We do the rest.

  1. A CV for this posting

    Written against Viant's own wording, from every piece of relevant proof in your profile.

  2. 25 readers review it

    Recruiter, hiring manager, skeptic and more read every draft, round after round. You get the best round.

    The review screen in CV Rocket: how each CV was read, round by round.

  3. We apply on Viant's form

    Our application engine gets through the hardest forms there are. Where a question needs you, AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

    An application in CV Rocket: every answer filled in on the employer's form.

  4. Every reply, sorted

    Viant's answer lands in your private mailbox, and we classify it on arrival: interview, question, rejection.

    The CV Rocket inbox: each employer reply classified as an interview, an action or a rejection.

  5. Reply with AI

    AI helps you write the email, checks it and sends it. We show you whether the recruiter read it.

  6. The interview in your calendar

    Full integration with your calendar. The invitation goes straight in.

    An interview invitation in the CV Rocket inbox, added to the candidate's calendar.
Get the CV for this job

From $25 per CV, paid once. No subscription.

Why it works

3×

more interviews than doing it yourself with ChatGPT.

ChatGPT writes a CV and never learns what happened to it. We see every reply. For each CV we know:

  • How it was written, and how the review scored it
  • When we applied, and how long after the posting went up
  • Which posting, which company, which city
  • Who got the interview, and who heard nothing

That is how we know which CVs get called.

Get the CV for this job

From $25 per CV, paid once. No subscription.

The numbers game

More applications. More interviews.

Every application goes out with its own CV, written for that posting and paid once. Send enough of them and the law of large numbers finds you the job.

Get the CV for this job
By hand5–10
With CV Rocket100
applications a day

Nearby

Live postings like this one

Same employer first, then the same role elsewhere.

Before you press

Straight answers

Get the CV for this job

From $25 per CV, paid once. No subscription.

What if my background isn't good enough?

We make the most of the background you have. The CV uses every piece of relevant proof your profile holds, and one of the 25 readers reads your whole profile and flags what the CV left out.

Do you really apply for me?

Yes, on the employer's own form, the hardest ones included. Where a question needs you, you answer it right there and AI suggests the best answer. Don't want us applying from our IP addresses? Use our Chrome extension: we apply straight from your own browser.

Is it a subscription?

No. You pay once per CV, from $25. Every application goes out with its own CV, written for that posting.

One job. One CV.
Paid once.

Pick the posting you want. We write for it, apply for you and catch the reply.

Get the CV for this job

From $25 per CV, paid once. No subscription.