20 beste vacatures voor de functie van quality manager in almere (nieuwe medewerkers gezocht)

Regulatory Affairs Manager (Expanded Access Programs)
myTomorrows —Amsterdam
- Fulltime
- Hybride werken
- Microsoft Word
- Microsoft Excel
- Engels
Senior Manager, Regulatory Affairs & Specifications (GB & EMENA)
McCain Foods Limited —Amsterdam
- Fulltime
- Master
- Bachelor
- Teammanagement
- Werk vanuit huis
Quality Assurance Manager
Optics11 —Amsterdam-Zuidoost
- Fulltime
- Engineering
- Master
- Bachelor
Snel solliciteren
Quality Lead, Distribution EMEA & Benelux
Santen —Amsterdam
- € 67.819 - € 93.251 per jaar
- Fulltime
- Hybride werken
- Engels
- Master
- Analytisch vermogen
Snel solliciteren
Kwaliteit- en Projectcoördinator
Epsa Procurement —Amsterdam
- € 4.800 - € 5.500 per maand
- Parttime
- Analytisch vermogen
- Bachelor
- Bedrijfskunde
Clinical FSP Quality Manager
IQVIA —Amsterdam
- Fulltime
- Bediening
- Computervaardigheden
- Engels
Global Quality Management System Digital Process Manager
Kraft Heinz Company —Amsterdam
- Kantoor
- Projectmanagement
- Agile
KAM Coördinator
Gebr. van der Lee VOF —Lelystad
- € 4.270 - € 5.700 per maand
- Fulltime
- Analytisch vermogen
- Organisatorische vaardigheden
QAQC Manager – Animal By-Products (ABP) & Waste
Argent Energy —Amsterdam
- Fulltime
- Hybride werken
- Analytisch vermogen
- Bachelor
- Continue verbetering
- Werk vanuit huis
Snel solliciteren
Global TPM/Supplier QA Product Manager
Abbott Laboratories —Weesp
- Fulltime
- Schrijfvaardigheden
- Engels
- Microsoft Office
Quality Engineer
GVB —Diemen
- € 3.553 - € 5.081 per maand
- Fulltime
- Hybride werken
- Mechanische ervaring
- Onderzoek
- Mechanische kennis
- Zorgverzekering
Sr. Kwaliteitsadviseur
UWV —Amsterdam
- € 4.616 - € 7.647 per maand
- Parttime
- Hybride werken
- Kantoor
- Analytisch vermogen
- Bachelor
- Reiskostenvergoeding
- Flexibele werkuren
10 dagen
QA/QC Manager
Sisk —Amstelveen
- Fulltime
- Civiele techniek
- Managementervaring
- Bouwmanagement
TPM QA Manager
Abbott Laboratories —Weesp
- Fulltime
- Managementervaring
9 dagen
R&D Compliance Officer
Alfen —Almere
- Online sollicitatie
- Hybride werken
- Informatica
- Engels
- Elektrotechniek
- Reiskostenvergoeding
10 dagen
Qualified Person
RnB Consultancy —Amsterdam
- € 6.000 - € 8.500 per maand
- Engels
- Bachelor
- Communicatieve vaardigheden
Snel solliciteren
kwaliteitspecialist
HEMA —Amsterdam Noord
- € 3.900 - € 5.500 per maand
- Fulltime
- Engels
- Analytisch vermogen
- Productkorting werknemers
- Reiskostenvergoeding
Logistics & Product Compliance Manager
Tesla —Amsterdam-Zuidoost
- Microsoft Excel
- Merchandising
- Engineering
10 dagen
Quality Assurance Coordinator - Kwaliteitscoordinator
Greif Nederland B.V. —Vreeland
- € 4.000 - € 4.500 per maand
- Fulltime
- Engels
- Analytisch vermogen
- Bachelor
- Reiskostenvergoeding
Snel solliciteren
6 dagen
Qualified Person (QP) – Cell Therapy
AstraZeneca —Amsterdam
- Fulltime
- Engels
- Master
- Analytisch vermogen

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Regulatory Affairs Manager (Expanded Access Programs)

myTomorrows
Amsterdam

Nu solliciteren

Vacaturegegevens

Fulltime

Kwalificaties

Microsoft Word
Microsoft Excel
Supplychain
Engels
Master
SharePoint
Gegevensverzameling
Communicatieve vaardigheden

Volledige vacaturetekst

About myTomorrows

myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options.

We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.

We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.

With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.

Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today.

The opportunity: Regulatory Affairs & Pharmacovigilance Manager

As the Regulatory Affairs and Pharmacovigilance Manager, you will be responsible for ensuring compliance of our processes with country-specific expanded access regulations globally. In this role, you'll be a key contributor to our regulatory and quality infrastructure, keeping us aligned with global legislation. You will be actively working together with Medical Affairs, Program Management, Quality Assurance, and Supply Chain and will report to the Director of Regulatory Affairs and Pharmacovigilance (Emily says hi).

What you will do in this role:

Support the development and execution of regulatory strategies for Expanded Access Programs (EAPs) involving biologicals, cell therapies, and synthetic drugs.
Act as the Regulatory Affairs and Pharmacovigilance expert for communications with clients (pharmaceutical companies) and submissions to Health Authorities, as well as cross-functional meetings and audits.
Prepare, compile, and submit regulatory dossiers for cohort and named patient Expanded Access Programs (EAPs) on behalf of clients.
Provide input and support for the regulatory strategy for setting up and executing EAPs (e.g., where, when, and how).
Collaborate with the Commercial team to support new EAPs.
Ensure timely and compliant handling of all regulatory and pharmacovigilance activities related to EAPs.
Stay up to date on relevant global laws, regulations, and guidelines impacting EAPs.
Assist in drafting, reviewing, and maintaining regulatory documentation and templates.
Liaise with the Pharmacovigilance service provider to ensure alignment and compliance.
Contribute to maintaining department documentation such as SOPs (Standard Operating Procedures), QIs (Quality Incidents), and CAPAs (Corrective and Preventive Actions).

What you bring to the table:

5+ years of relevant experience in Regulatory Affairs, including experience in Expanded Access.
Working knowledge of fundamental principles of Pharmacovigilance is required.
Solid understanding of national and international legislation and regulation relating to Expanded Access
A Bachelor’s or Master's degree in Life Sciences or a related field
Experience working directly with clients or external stakeholders in a professional setting
Strong communication skills (written and verbal) in English; able to convey complex topics clearly to both internal teams and external parties. Knowledge of additional languages is a plus
Comfortable collaborating across teams and working in a cross-functional environment
Proactive problem solver with the ability to identify potential regulatory or operational challenges early and suggest practical solutions
Familiarity with Microsoft 365 tools (e.g., Word, Excel, Teams, SharePoint)

What we offer:

Impactful work that helps patients gain access to potentially lifesaving treatments.
International work environment, scale-up energy and flat organizational structure which encourages creativity and accountability.
Competitive salary, annual performance bonus and an Employee Stock Option Plan.
Great career development opportunities in a fast-growing company.
Learning and development budget alongside internal knowledge sharing sessions.
Hybrid working model if you're in the Netherlands.
Policies to support working parents.
Healthy lunch at the thriving Amsterdam office.
Unlimited access to professional guidance by certified psychologists via OpenUp
Enjoy monthly events hosted by our vibrant Culture Club as well as an annual ‘myTomorrowland’ company-wide celebration!

Equal opportunities

myTomorrows is an Equal Opportunity Employer and, beyond upholding discrimination-free practices, we are committed to cultivating a workplace where difference and diversity are protected and celebrated. The best work comes from our best selves, and we go to great lengths in supporting our team members to be just that.

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quality manager vacatures in almere

Regulatory Affairs Manager (Expanded Access Programs)

Senior Manager, Regulatory Affairs & Specifications (GB & EMENA)

Quality Assurance Manager

Quality Lead, Distribution EMEA & Benelux

Kwaliteit- en Projectcoördinator

Clinical FSP Quality Manager

Global Quality Management System Digital Process Manager

KAM Coördinator

QAQC Manager – Animal By-Products (ABP) & Waste

Global TPM/Supplier QA Product Manager

Quality Engineer

Sr. Kwaliteitsadviseur

QA/QC Manager

TPM QA Manager

R&D Compliance Officer

Qualified Person

kwaliteitspecialist

Logistics & Product Compliance Manager

Quality Assurance Coordinator - Kwaliteitscoordinator

Qualified Person (QP) – Cell Therapy

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van quality manager in almere

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