Process Engineer I

Your new company

Our client is a company that 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. They have 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.

Your new role

We are searching for a highly affective Process Engineer for whom compliance thinking and wanting to implement improvements is second nature. The successful candidate will provide process and product expertise for GMP manufacturing, technology transfers and process validations for cell therapy products. You will do this by performing root-cause investigations and deviation resolution for complex problems and collaborating with technical and operational stakeholders, writing SOP’s, batch records and other operational-related documents. You will participate in the evaluation of new technology and process automation for the introduction to GMP manufacturing. You will investigate and coordinate the resolution of deviations through comprehensive use of Root Cause Analysis tools. You will also devise and implement CAPAs to address root causes and ensure effectiveness.

What you'll need to succeed

The ideal candidate for this role has completed a BSc in Biochemical Engineering, Chemical Engineering, Biotechnology or equivalent an Engineering degree is a strong plus. Over the past years, has gained 2-3 years’ relevant process engineer experience within a Pharmaceutical/GMP Manufacturing Site. Furthermore, they will have:

Prior work experience in cell culture, cell therapy and/or aseptic processing.
Proven technical knowledge & experience with cGMP compliance.
Experience in leading investigations, writing deviation reports, change controls, and corrective actions.
Excellent communication skills and can work in cross-functional teams to obtain project deliverables.
Knowledge of scientific and engineering principles.
Self-motivated, detail-oriented and can think critically and demonstrate troubleshooting and problem-solving skills.

What you'll get in return

Hays Detachering | This is a project that will start with a contract for 12 months through Hays. Extension to stay within the department is anticipated. In this position, you will get a competitive salary and your travel expenses are covered.

What you need to do now

If you are interested in this role as Process Engineer, click ‘Apply now’ to send an up-to-date CV, or give us a call! If this job isn’t quite right for you, are you still looking for a new position? Please contact us for a confidential discussion about your career.

#LI-DNI

Klik hier om het privacybeleid van Hays te lezen, welke gedetailleerde informatie bevat over hoe we uw persoonlijke gegevens gebruiken en beschermen, en uw rechten in verband hiermee.