Kite, a Gilead company, is dedicated to achieving one of the most ambitious goals of 21st century medicine: curing cancer. This mission is at the heart of everything they do, from early research to product development. Kite has been at the forefront of cancer immunotherapy and today are a leader in engineered T cell therapy, changing the paradigm of cancer treatment with what is potentially the biggest breakthrough since the introduction of combination chemotherapy more than 60 years ago. With an unrelenting drive and a singular focus on cell therapy, our team is executing on our strategy to bring life-saving therapies to patients.
With their brand-new production site in Hoofddorp and the R&D laboratories in Amsterdam, Kite is dreaming big. Now you can get the chance to be a part of this journey!
Your new role
We are searching for a motivated Validation Engineer to join Kite Pharma in the global fight against cancer. You will be involved in creating and executing qualification protocols (IOQ / PQ), including identification and resolution of non-conformances/deviations. You will also provide equipment, system and facility qualification guidance and strategy during project planning and development phases. Alongside this you will be responsible for reviewing technical documentation including protocols & summary reports for IOQ / PQ testing, including the validation of SOPs. In addition, you will perform temperature mapping and other miscellaneous validation activities. You will also be responsible for managing contractors performing equipment and system qualifications and reporting the status and progress of qualification activities or projects to the leadership team. Other responsibilities include:
Perform investigations and implement corrective actions related to CAPAs and deviations
Develop technical specifications
Support the execution of engineering projects
Execute periodic reviews
Perform Risk assessments
Other duties as assigned
What you’ll need to succeed
The successful candidate will hold a MBO 4 with at least 6 years relevant experience as a Validation Engineer in a Pharmaceutical environment or HBO with at least 4 years’ experience. Experience in GMP environment is a must and if you have experience with cell therapy it is considered a plus. Previous experience in validation is required.
What you’ll get in return
Hays Detachering | This is a project that will start with a contract for 6 months through Hays. Extension to stay within the department is anticipated. At this position, you will get a salary of €65,880 per year, based on 40 hours of work and your travel expenses are covered.
What you need to do now
If you are interested in this role as Validation Engineer II, click ‘Apply now’ to send an up-to-date CV, or give us a call! Is this job isn’t quite right for you, but are you still looking for a new position? Please contact us for a confidential discussion on your career.
Senioriteitsniveau
Senior medewerker
Soort baan
Fulltime
Functie
Productie, Wetenschap en Productie
Bedrijfstakken
Biotechnologisch onderzoek en Geneesmiddelenproductie
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