Medical Device Quality Engineer
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Build our future together:
At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. The Medical Device Quality Engineer provides Quality Assurance support and guidance to ensure compliance in support of combination products for biological therapeutics developed in-house and in collaboration with partners and CMO’s.
When & where:
Location: East Greenbush, New York, United States
Work model: Monday-Friday, 8:00 am - 4:30 pm
Discover your role:
Reviews and supports Design and Development documentation for compliance to internal procedures and regulations.
Reviews activities related to Design Verification, Design Validation and Design Transfer during development of medical devices and combination products.
Provides quality and technical support for the evaluation of change assessments for medical devices and combination products.
Authors, leads and contributes to Risk Management activities including FMEAs.
Reviews and coordinates with QA and various laboratory groups for test method development and test method validations.
Ensures proper justification of statistical analysis and hypothesis testing.
Aids in establishing proper statistical controls in development and transfer to manufacturing processes.
Supports scientific, complaint and test failure investigations for medical devices and combination products.
Supports actions required because of updates to standards and/or new applicable standards.
Supports and contributes to CI initiatives for Med Device Quality.
Performs tata/statistical/trend analysis as needed.
Ensures work product meets regulations.
Writes Quality Procedures, as applicable.
This role requires:
Bachelor’s degree in engineering.
Experience working in either combination products or medical devices.
Associate Engineer: 0 – 2 years of experience
Engineer: 2 years of experience
Senior Engineer: 5 years of experience
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.
Where necessary, we disclose salary ranges for roles in all countries in which we operate. The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits. Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.
As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.
For jobs in Canada: this posting is for an existing position.
Salary Range (annually)
$66,200.00 - $143,900.00
Job details
How this role compares
Computed from every other active Quality role in our database, not just this employer's listings.
We currently track 1507 comparable Quality roles across 149 biopharma companies.
Salary context
262 of 1507 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 1507 comparable roles
+ 47 more countries
Seniority mix
737 of 1507 peers have a known seniority level
Therapeutic area mix
3 of 1507 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.