or apply directly on quip's site. We never take the application ourselves.
Is this posting real?
- This role has been open
- 7 days quip's roles stay open a median of 45 days
- Reposted
- No
- Salary listed
- Yes 100% of quip's roles list one
- Ghost-job risk at quip
- high 5 stale, 0 reposted of 7 open
- Hiring momentum
- 8 roles opened in the last 90 days ↑ up vs. the prior 90 days
- Last confirmed on the employer's board
- 2026-09-17
Measured from postings appearing on and disappearing from quip's own greenhouse board since 2026-08-03. Full hiring picture for quip.
About this role
As a Sr. Regulatory & Quality Systems Engineer at quip, you will lead the regulatory strategy for product integrity, ensuring compliance and safety from initial filings to post-market surveillance. Your responsibilities include managing FDA compliance for Class I devices, overseeing contract manufacturers' quality systems, and serving as the quality sign-off authority in new product development. This role requires a strategic mindset to build and enhance quip's regulatory and quality infrastructure as the company expands into new markets.
- benefits
- 5/5
- freshness
- 5/5
- career value
- 4/5
- role clarity
- 5/5
- pay transparency
- 5/5
Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of quip as an employer.
What you need
- 6+ years experience in Regulatory and/or Quality Engineering / Systems management
- Knowledge of FDA 21 CFR Part 820 and ISO 13485 or demonstrated ability to learn and lead compliance to these standards
- Familiarity with FDA Medical Device Reporting (21 CFR Part 803), UDI/GUDID (21 CFR Part 830), and establishment registration & listing (21 CFR Part 807) for Class I devices
- High cavitation injection molding and machining process experience
- Strong communication skills to present quality risks to executive leadership
- Ability to travel internationally 2-3 times per year to be on-site at suppliers
Nice to have
- Experience with IPX rated products that require defense against moisture ingress
- Experience with FDA regulations for dietary supplements or OTCs
- Experience with FDA, ADA, WERC account ownership
- Experience working with Asian suppliers and contract manufacturers
What you get
- Hybrid working environment, with an office located in the heart of DUMBO with breathtaking views of Manhattan Bridge
- Year round early “summer Fridays”
- WiFi enabled rooftop
- Competitive medical benefit package
- Commuter benefits for parking & transit
- Competitive paid parental leave policy for qualifying employees
Worth weighing
- Full-time on-site Monday–Thursday with remote work on Fridays
- No salary listed beyond the range of $150k-$165K
- Position not eligible for immigration sponsorship
- Role involves significant responsibility in regulatory compliance and quality systems management
Summarised from quip's posting. Read the full original.
Listed by quip on their greenhouse job board, last confirmed open on 2026-09-17. PitchMeAI is not the employer.
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