We are Nostics

We are a young and international team on a mission to change the world for millions around the globe by providing new, faster and reliable diagnostics.  Ready to join Nostics?

”Be aware: there are people/organizations pretending to work for us and conducting interviews and asking for personal information. We have been notified about someone by the name of Carlos Davis doing this and using the website nostics.us (which is NOT owned by us), but there might be others. Only apply directly through the links below. When in doubt, check our LinkedIn page to verify who really works at Nostics. Take care and we are looking forward to your application!

Vacancies

QA Manager

📍 Location: Amsterdam
🕒 Timing: As soon as possible
💼  40 hours/week

 

About Nostics

At Nostics, we’re building smarter, faster diagnostics for a healthier future. We are developing the world’s first clinical diagnostic platform powered by Surface Enhanced Raman Spectroscopy (SERS), enabling rapid, label-free identification of bacteria directly from patient samples in under 10 minutes. Our first product, DUTI (Direct UTI Identification), targets urinary tract infections: one of the most common primary care presentations and a major driver of inappropriate antibiotic prescribing.

We are a growing startup in Amsterdam, now preparing for regulatory submission.

 

The Role

We are looking for a QA Manager to lead quality at Nostics. You will own our quality management system under ISO 13485, the IVDR and FDA 21 CFR Part 820, and build a culture of compliance and continuous improvement.

This is a hands-on role for a pragmatic leader with solid IVD experience. You set direction, keep compliance proportionate to a startup, and in the first phase do much of the day-to-day QA work yourself.

 

Responsibilities

As QA Manager, you will:

·     Build, maintain and improve the QMS, including CAPA, nonconformances and change control

·     Act as Management Representative and advise management on quality risks and priorities

·     Run internal and supplier audits and host notified body audits

·     Keep the company audit ready and support regulatory submissions

·     Own our eQMS and use automation and AI tools where they help

·     Report quality KPIs and build the QA team as the company grows

 

Requirements

What we’d love you to bring:

·     A Master’s or Bachelor’s degree in life sciences, engineering or a related field

·     5+ years in quality management under ISO 13485, including at least 2 years in IVD under the IVDR

·     Experience hosting notified body audits and supporting CE submissions; FDA experience is a plus

·     Strong knowledge of ISO 13485, IVDR, 21 CFR Part 820 and ISO 14971

·     Proven leadership: you take ownership and hold colleagues and management to account

·     A pragmatic, hands-on approach and affinity with automation and AI

·     Qualified internal auditor (lead auditor preferred); fluent English, Dutch is an asset

 

What we offer

·     A key role in bringing a first-of-its-kind diagnostic to market

·     Ownership, direct access to the management team and room to build the QA team

·     A collaborative, science-driven team

·     Competitive salary, 8% holiday allowance and 30 holidays

·     Collective pension plan and a mobility allowance or free public transport card

 

Why join?

Antibiotic resistance is one of the defining health challenges of our time. Our diagnostics help clinicians make faster, better treatment decisions and reduce unnecessary antibiotic use. A strong QMS is what gets this product to patients safely.

 

Interested?

If you are a pragmatic quality leader with IVD experience and want to shape quality at the stage where it defines the company, we would love to hear from you.

Apply via the button below!

Apply

QA Specialist

📍 Location: Amsterdam
🕒 Timing: within two months, 3–6 months (flexible)
💼 16–40 hours/week

 

About Nostics

At Nostics, we’re building smarter, faster diagnostics for a healthier future. We are developing the world’s first clinical diagnostic platform powered by Surface Enhanced Raman Spectroscopy (SERS), enabling rapid, label-free identification of bacteria directly from patient samples in under 10 minutes. Our first product, DUTI (Direct UTI Identification), targets urinary tract infections: one of the most common primary care presentations and a major driver of inappropriate antibiotic prescribing.

We are a growing startup in Amsterdam, now preparing for regulatory submission.

 

The Role

We are looking for a QA Specialist to run our day-to-day quality processes together with our QA lead. You make sure documents are correct, records do not stall and audit files are ready when needed.

The role offers room to grow: as you develop, you take on more responsibility, such as owning CAPA and leading internal audits.

 

Responsibilities

As QA Specialist, you will:

·     Check, route and register documents in the eQMS

·     Support and track nonconformances, deviations, CAPAs and change records

·     Maintain training records and supplier quality files

·     Co-audit in the internal audit programme and prepare audit files

·     Act as key user of our eQMS and collect data for quality KPIs

 

Requirements

What we’d love you to bring:

·     A Bachelor’s degree in life sciences, engineering or equivalent

·     2+ years in QA in a regulated environment (ISO 13485 preferred; ISO 9001 or GMP welcome)

·     Hands-on eQMS experience

·     Precise and structured, with the confidence to hold colleagues to a process

·     Fluent English; Dutch is an asset

 

What we offer

·     Room to grow, with coaching from an experienced QA lead

·     Broad exposure to a full QMS in a company preparing for market

·     A collaborative, science-driven team

·     Competitive salary, 8% holiday allowance and 30 holidays

·     Collective pension plan and a mobility allowance or free public transport card

 

Why join?

Antibiotic resistance is one of the defining health challenges of our time. Our diagnostics help clinicians make faster, better treatment decisions and reduce unnecessary antibiotic use. Here you learn quality management from the ground up, in a company where your work visibly matters.

 

Interested?

If you are precise, like structure and want to grow in quality assurance at a MedTech startup, we would love to hear from you.

Apply via the button below!

Apply

Working at Nostics

Diverse workforce

Nostics is committed to recruiting and retaining a diverse workforce, and we look for candidates who have a high level of demonstrated cultural competency. People of color, people with disabilities, women, and lesbian, gay, bisexual, and transgender people are encouraged to apply. All applicants will be considered without regard to race, color, national origin, religion, sexual orientation, sex, marital or parental status, disability, gender identity or expression, age, or any other basis prohibited by law.

Office and lab-accessibility

We are based on the 5th floor with accessibility by elevator straight from the car-park. The office and lab are equal-floors accessible without stairs, steps or other hurdles. In case you have questions regarding accessibility please give us a call or ask us during the interview process. 

Commuting to work

We have a few parking spots available and we have a train station on a couple minutes walking distance. Commuting by car is possible but public transport is highly preferred.