20 beste vacatures voor de functie van kwaliteitsmanager in 2266 leidschendam (nieuwe medewerkers gezocht)

Quality Specialist Development
Pharming Group —Leiden
- € 72.000 - € 100.000 per jaar
- Master
- Communicatieve vaardigheden
3 uur
QA/QC Officer
Vergeer Holland —Reeuwijk
- € 3.457,00 - € 4.506,67 per maand
- Parttime
- ERP systemen
- Analytisch vermogen
- Computervaardigheden
QC Engineer Maasvlakte
Sif Group —Rotterdam
- € 4.300 - € 6.000 per maand
- Fulltime
- AutoCAD
- Engineering
- Engels
QA specialist
Gepo Vleeswaren —Nieuw-Vennep
- Parttime
- Analytisch vermogen
- Bachelor
- Communicatieve vaardigheden
QA/QC Coördinator
VINCI Energies —Rotterdam
- Engels
- Elektrotechniek
- Winstdeling
Product Assurance Engineer
ISISPACE —Delft
- € 2.947 - € 3.658 per maand
- Fulltime
- Hybride werken
- Bachelor
- Communicatieve vaardigheden
Snel solliciteren
ILS Quality & Compliance Engineer
Destinus —Katwijk aan Zee
- Fulltime
- Hybride werken
- Engineering
- Engels
- Bachelor
Snel solliciteren
QA Manager
ADM —Rotterdam
- Engels
- Bachelor
- Managementervaring
Supplier Quality Manager
Priva —De Lier
- € 5.800 - € 7.000 per maand
- Fulltime
- Hybride werken
- ERP systemen
- Engels
- Analytisch vermogen
- Reiskostenvergoeding
Snel solliciteren
QESH Manager
Group of Butchers —Delft
- € 4.631 - € 7.461 per maand
- Engels
- Productie
- Communicatieve vaardigheden
Snel solliciteren
Kwaliteitsadviseur
Klant Contact Diensten —Zoetermeer
- € 3.340 - € 5.178 per maand
- Parttime
- Hybride werken
- Microsoft Excel
- Kantoor
- Analytisch vermogen
Snel solliciteren
3 dagen
Product Assurance Process Engineer (Space Systems)
cosine —Sassenheim
- Hybride werken
- Budget voor professionele ontwikkeling
Snel solliciteren
Quality Systems Engineer
Cabot Corporation —Rotterdam
- Fulltime
- Engineering
- Analytisch vermogen
- Bachelor
Food Safety Manager
Roveg Fruit —Waddinxveen
- Fulltime
- Engels
- Master
- Bachelor
- Reiskostenvergoeding
Adviseur Kwaliteit en Veiligheid
Huize Winterdijk —Gouda
- Parttime
- Communicatieve vaardigheden
QAQC Coördinator Techniek
Ballast Nedam —Rotterdam
- € 4.750 - € 6.000 per maand
- Fulltime
- Hybride werken
- Elektra
- Bachelor
- Communicatieve vaardigheden
Snel solliciteren
Kwaliteitsmedewerker
MegaMix Randstad BV —Gouda
- € 4.000 - € 5.500 per maand
- E-mail
- Productie
- Reiskostenvergoeding
Snel solliciteren
8 uur
Regulatory Affairs Project Manager
Perrigo —Rotterdam
- Thuiswerk
- Engels
- Master
- Projectmanagement
1 uur
Supplier Quality Engineer
Priva —De Lier
- € 3.600 - € 4.800 per maand
- Fulltime
- Hybride werken
- ERP systemen
- Engels
- Analytisch vermogen
- Reiskostenvergoeding
Snel solliciteren
Manager Supplier Quality Engineering
Priva —De Lier
- € 4.800 - € 6.100 per maand
- Fulltime
- Hybride werken
- ERP systemen
- Engels
- Analytisch vermogen
- Reiskostenvergoeding
Snel solliciteren

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Quality Specialist Development

Pharming Group
Leiden

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Vacaturegegevens

€ 72.000 - € 100.000 per jaar
3 uur geleden

Secundaire arbeidsvoorwaarden

Pensioen

Kwalificaties

Leveranciersmanagement
Supplychain
Biotechnologie
Master
Kwaliteitsborging
Farmacie
Communicatieve vaardigheden

Volledige vacaturetekst

Contribute to the development of innovative therapies for patients with rare diseases

Are you an experienced Quality Assurance professional with a strong GMP background and experience in the pharmaceutical or biopharmaceutical industry? Would you like to play a key role in the development of innovative therapies that make a real difference in patients' lives worldwide? If so, we would love to hear from you.

About Pharming

Pharming is a global biotechnology company dedicated to developing innovative therapies for people living with rare diseases. Our mission is to improve patients' lives by addressing significant unmet medical needs. Quality, collaboration, and innovation are at the heart of everything we do.

Your work environment

As a Quality Specialist Development, you will be part of the Quality Assurance team within Pharming Technologies B.V. and serve as the dedicated QA Business Partner for one of our CMC Development Teams (Chemistry, Manufacturing & Controls). In this highly collaborative role, you will provide strategic quality oversight and expert guidance throughout the product lifecycle, from development and validation through technology transfer and commercialization. You will play a key role in influencing project decisions, and ensuring alignment with Pharming's quality standards and applicable EU and US GMP requirements.

You will work closely with colleagues across QA, CMC, Manufacturing, QC, Regulatory Affairs, Supply Chain, and R&D, while also collaborating with external partners, including contract manufacturers, laboratories, and suppliers.

What will you do?

Provide strategic QA guidance to the CMC Development Team throughout development, technology transfer and commercialization activities;
Support and review development, technology transfer, validation, and commercial manufacturing activities;
Contribute to the maintenance and continuous improvement of the Quality Management System, including quality documentation and quality agreements;
Perform supplier qualifications and audits, and assess quality and compliance risks across internal and external stakeholders;
Advise project teams on GMP, quality, and compliance topics, acting as a trusted coach and subject matter expert;
Drive and support quality improvement initiatives while working closely with PQA Operations.

What do you bring?

Bachelor's or Master's degree in Pharmacy, Biotechnology, (Bio)Chemistry, Biopharmaceutical Sciences, Engineering, or a related field;
At least six years of experience in a pharmaceutical or biopharmaceutical environment, including several years in Quality Assurance;
Strong knowledge of EU and US GMP regulations and experience in pharmaceutical development, validation, and/or commercial manufacturing;
Experience with audits, supplier management, and quality systems such as SAP, MasterControl, or similar platforms;
Excellent communication skills, a proactive mindset, and the ability to influence stakeholders at different levels of the organization.

What can you expect from us?

A challenging role within an innovative international biotechnology company.
The opportunity to contribute directly to the development of therapies for patients with rare diseases.
A competitive salary ranging from €72,000 to €100,000 gross per year, including 8.33% holiday allowance (based on a full-time position);
Annual bonus scheme;
33 vacation days per year (based on a full-time position);
An excellent pension plan;
Opportunities for personal and professional growth;
A collaborative, purpose-driven environment where your work helps bring innovative therapies to patients around the world.

Interested?

Are you excited about this opportunity and do you recognize yourself in this profile? We look forward to receiving your application.

Please note: Due to the holiday period, applications will be reviewed from mid-August onwards. We appreciate your interest and will contact you as soon as possible regarding the next steps in the recruitment process.

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kwaliteitsmanager vacatures in 2266 leidschendam

Quality Specialist Development

QA/QC Officer

QC Engineer Maasvlakte

QA specialist

QA/QC Coördinator

Product Assurance Engineer

ILS Quality & Compliance Engineer

QA Manager

Supplier Quality Manager

QESH Manager

Kwaliteitsadviseur

Product Assurance Process Engineer (Space Systems)

Quality Systems Engineer

Food Safety Manager

Adviseur Kwaliteit en Veiligheid

QAQC Coördinator Techniek

Kwaliteitsmedewerker

Regulatory Affairs Project Manager

Supplier Quality Engineer

Manager Supplier Quality Engineering

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van kwaliteitsmanager in 2266 leidschendam

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