20 beste vacatures voor de functie van kwaliteitsmanager in leiderdorp, zh (nieuwe medewerkers gezocht)

QA Specialist
NecstGen —Leiden
- € 3.413 - € 5.409 per maand
- Fulltime
- Engels
- Master
- Analytisch vermogen
- Reiskostenvergoeding
Snel solliciteren
Manager Quality & Training op Schiphol
Trigion —Schiphol
- € 7.000 - € 9.000 per maand
- Parttime
- Management
- Kantoor
- Analytisch vermogen
- Gezondheidsprogramma
Manager Quality, Health, Safety, Security and Environment
Swissport International AG —Schiphol
- Vanaf € 5.000 per maand
- Fulltime
- Hybride werken
- Engels
- Leidinggevende ervaring
- Organisatorische vaardigheden
- Reiskostenvergoeding
- Zorgverzekering
Kwaliteitscoördinator
Schakenbosch —Leidschendam
- Tot € 5.410,39 per maand
- Parttime
- Verzorging
- Analytisch vermogen
- Bachelor
- Zorgverzekering
14 dagen
Senior Kwaliteitsmanager in Projecten
Yunex Traffic —Zoetermeer
- € 4.539 - € 5.332 per maand
- Parttime
- Kantoor
- Communicatieve vaardigheden
- Reiskostenvergoeding
Kwaliteitsmanager (parttime) (v/m/x)
Conxillium Group —Capelle aan den IJssel
- € 3.300 - € 5.250 per maand
- Fulltime
- Hybride werken
- Kantoor
- Bachelor
- Communicatieve vaardigheden
- Bedrijfsfitness
- Budget voor professionele ontwikkeling
QA Specialist III Deviation and Front-Line Support
Kite Pharma —Hoofddorp
- Weekendbeschikbaarheid
- Hybride werken
- Management
- Laboratoriumervaring
- Microsoft Office
Kwaliteitsmanager
Bali Food —Den Haag
- € 15,50 - € 19,50 per uur
- Parttime
- Engels
- Projectmanagement
- Organisatorische vaardigheden
- Kosteloos parkeren
- Productkorting werknemers
Snel solliciteren
Quality assurance medewerker
Mosadex —Leiden
- € 4.000 - € 5.500 per maand
- Fulltime
- Hybride werken
- Bachelor
- Zonder diploma
- APIs
Snel solliciteren
Materials & Welding Engineer
NEM Energy —Zoeterwoude
- Fulltime
- Hybride werken
- Laboratorium
- Engels
- Bachelor
Snel solliciteren
KAM-Coördinator
Comtest Engineering —Zoeterwoude
- € 4.000 - € 5.000 per maand
- Parttime
- Engels
- Communicatieve vaardigheden
Snel solliciteren
Pharmaceutical Quality Assurance Manager (Kwaliteitsmanager)
Van Pharma B.V. —Zoetermeer
- Hybride werken
- Engels
- Analytisch vermogen
- Bachelor
Snel solliciteren
9 dagen
(Sr) Validation Engineer
HAL Allergy —Leiden
- Engels
- Analytisch vermogen
- Bachelor
Junior Quality Engineer (3-shifts)
Logoplaste —Zoetermeer
- Fulltime
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Reiskostenvergoeding
Snel solliciteren
Quality Control Scientist (Biotech & In Vitro Immunology)
MAT Research —Leiden
- Fulltime
- Doctor
- Master
- Analytisch vermogen
Snel solliciteren
Manager, Regulatory Affairs EMEA
Thermo Fisher Scientific —Bleiswijk
- Fulltime
- Engels
- Projectmanagement
- Bachelor
QA specialist Bakkerij
Hoogvliet —Bleiswijk
- € 3.100 - € 3.800 per maand
- Parttime
- Fysiek solliciteren
- Analytisch vermogen
- Bachelor
- Reiskostenvergoeding
- Personeelskorting
Manager - IT Quality and Computerized Systems Validation
Bristol-Myers Squibb —Leiden
- Fulltime
- Hybride werken
- Microsoft Excel
- Engineering
- ERP systemen
Regulatory & Homologation Manager – Europe (Passenger Vehicles / New Energy)
BYD Europe —Hoofddorp
- Spaans
- Engels
- Master
Senior Quality Advisor
Subsea 7 —Zoetermeer
- Continue verbetering
- Managementervaring
- Communicatieve vaardigheden
8 dagen

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QA Specialist

NecstGen
Leiden

Snel solliciteren

Vacaturegegevens

Fulltime
€ 3.413 - € 5.409 per maand

Secundaire arbeidsvoorwaarden

Reiskostenvergoeding
Pensioen

Kwalificaties

Biotechnologie
Engels
Master
Analytisch vermogen
Kwaliteitsborging
Communicatieve vaardigheden

Volledige vacaturetekst

Are you an enthusiastic QA Specialist? Do you enjoy working in a scale-up environment? Do you have GMP experience? Are you based in the Leiden area? Then keep reading!

Who are we?

NecstGen is a leading CDMO (Contract Development and Manufacturing Organization) focused on process development and GMP manufacturing of cell and gene therapies. We are an independent, non-profit organization with a state-of-the-art facility in Leiden, specifically designed to develop, manufacture, and deliver these complex therapies to patients.

NecstGen is an independent subsidiary of the Leiden University Medical Center (LUMC). Thanks to this independent position, we can fully focus on innovation and accessibility in cell and gene therapy. Our location at the Leiden Bio Science Park, one of Europe’s largest life sciences clusters, offers direct access to a network of experts, partners, and emerging talent.

By investing in advanced manufacturing technologies and strategic collaborations, we support academic institutions, start-ups, and biopharmaceutical companies in scaling up their innovative therapies. Our expertise and flexible approach enable organizations to execute complex manufacturing processes efficiently and according to the highest quality standards.

Working at NecstGen means:

Contributing to the future of healthcare with innovative cell and gene therapies.
Working in a modern, high-tech environment with the latest equipment.
Being part of a close-knit and motivated team where collaboration and growth are central.
The opportunity for professional development in a fast-growing sector with many career advancement opportunities.
Working at a strategic location in the Leiden Bio Science Park, at the heart of an international network of experts and companies.

What will you do?

As a QA Specialist you will:

Support effective implementation, monitoring, reporting, maintenance and administration of the quality management system;
Support monitoring and reporting, of compliance of the organization and its activities with GMP and other relevant legislation and regulations;
Act as trainer, coach and expert on QA related matters and systems for other NecstGen colleagues;
Ensure effective and timely handling of quality issues (deviations, complaints) and monitor the application and efficiency of corrective and preventive actions;
Support creation of SOPs, policies and other QA related documentation (writing, review, approval) in alignment with applicable GxP guidelines. Identify documents which need to be created or updated and ensure this is organized;
Support (review and approval) of Risk Assessments, qualification/validation protocols and reports of analytical methods, equipment and facility, QC testing documentation, specifications, materials and release documentation, batch records etc, to ensure compliance with applicable guidelines and procedures;
Assist compilation of documentation for QP disposition;
Represent QA department in projects;
Propagate continuous improvement by identifying and communicating areas for improvement. Initiate, formulate and implement new processes and procedures within area of expertise;
Participate in the Supplier Qualification process;
Support the organization, hosting and reporting of inspections and audits and coordination of related CAPAs;
Conduct internal audits, and inspections at suppliers and third parties to whom GMP activities are outsourced; qualification and monitoring of those suppliers and third parties.

Who are you?

MSc in Biotechnology, chemistry, biopharmaceutics or equivalent;
Proficiency in cGMPs, GDPs and regulations promulgated by the EMA or equivalent regulatory Agencies;
Three years of recent experience in (bio)pharmaceutical environment with at least one year of recent experience in Quality Assurance;
Experience within a sterile manufacturing environment, preferable ATMPs (biologicals, vaccines, injectables, parenteral);
Good communication skills in English (in writing and verbally);
Willingness to travel: occasional travelling may be required to support the auditing program.

What do we offer you?

A monthly salary between €3,413 and €5,409 (based on a 36-hour workweek);
A 13th-month bonus paid in November;
26 vacation days for a full-time (36-hour) position;
A premium-free pension scheme;
Travel allowance for commuting (from 10 km) of €0.23 per km and full reimbursement of public transport costs;
Various flexible employment benefits in addition to the above.

Questions?
Don't hesitate to contact Diederik Pardon at [email protected] for more information.

Snel solliciteren

Verfijn je zoekopdracht

kwaliteitsmanager vacatures in leiderdorp, zh

QA Specialist

Manager Quality & Training op Schiphol

Manager Quality, Health, Safety, Security and Environment

Kwaliteitscoördinator

Senior Kwaliteitsmanager in Projecten

Kwaliteitsmanager (parttime) (v/m/x)

QA Specialist III Deviation and Front-Line Support

Kwaliteitsmanager

Quality assurance medewerker

Materials & Welding Engineer

KAM-Coördinator

Pharmaceutical Quality Assurance Manager (Kwaliteitsmanager)

(Sr) Validation Engineer

Junior Quality Engineer (3-shifts)

Quality Control Scientist (Biotech & In Vitro Immunology)

Manager, Regulatory Affairs EMEA

QA specialist Bakkerij

Manager - IT Quality and Computerized Systems Validation

Regulatory & Homologation Manager – Europe (Passenger Vehicles / New Energy)

Senior Quality Advisor

Ik wil de nieuwste vacature-alerts ontvangen voor de functie van kwaliteitsmanager in leiderdorp, zh

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