Laboratory & Quality IT System Engineer
- Rotterdam
- Contract
- Life Sciences
This vacancy has now expired
Are you local to the Netherlands and would you like to join a leading biopharmaceutical company in their mission to make a difference, changing lives through their scientific pursuits? Our client, a discoverer and developer of innovative medicines, are recruiting for a Laboratory & Quality IT System Engineer to join their brand-new build cell therapy project on a 6-8 month contractual basis.
Laboratory & Quality IT System Engineer Responsibilities:
- Provide support and enhancements for the administration of benchtop instrumentation applications, PC hardware, and IT administrative tools within a GxP environment. Support would encompass various instrument types such as cell counters, plate readers, and flow cytometers throughout the site which include laboratory and manufacturing buildings.
- Provide support of assets and utilise client systems to support changes, incidents, problems, and asset management activities for the support of benchtop equipment and lab and quality systems, as well as provide on-call support, as needed, for commercial operations.
- Liaise with global partners within the clients organisation to align on solutions and implementation plans for benchtop instrumentation and performs system installations, configurations, administrative and support functions including system validation lifecycles and training and provide supporting activities within the quality management system (Infinity).
- Provide local administrative support and liaison with global partners for the site quality systems and quality control supporting applications completing tasks such as application periodic reviews, user access reviews, and account administration.
- The ability to participate in small size projects and enhancements.
- Knowledge of Data Integrity guidance, GxP compliance, Software Development Life Cycle, and Good Documentation Practices
- Understanding of SOPs, cGMPs and other compliance requirements and regulatory guidelines (FDA, EU) and the ability to work and manage within a regulatory environment.
- Proven implementation and life cycle planning of lab and quality systems such as (LES, Empower, DCA, NuGenesis or similar), support of cyber security actions, upgrade of instrument PCs and peripherals.
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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Andre
I manage this role.