Laboratory Equipment IT Engineer, Regeneron Cell Medicines

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Laboratory Equipment IT Engineer, Regeneron Cell Medicines, Cambridge

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Client:Location:

Cambridge, United Kingdom

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

6892504e8e0f

Job Views:

5

Posted:

29.06.2025

Expiry Date:

13.08.2025

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Job Description:

We are seeking a motivatedLaboratory Equipment IT Engineerto support and maintain Building Management, Clinical Manufacturing Equipment and data acquisition/monitoring systems that support Clinical Manufacturing and Research and Development (R&D). This role is a part of Regeneron Cell Medicines (RCM), a newly formed R&D unit within Regeneron to advance cell therapies and combination approaches in oncology and immunology. We hope you are excited to serve as the technical SME as well as operate at the system administration, engineering, and management levels.

As an Laboratory Equipment IT Engineer, a typical day might include the following:

Supporting all manufacturing and QC equipment within RCM’s 30,000 SF Phase 1 clinical manufacturing facility

Maintaining System documentation, including converting User Requirement Specifications to a Detail Design Specification, writing Configuration Test Plans, and summary reports

Leading IT Applications systems security access and periodic audit trail reviews

Performing investigations relating to manufacturing deviations and anomalies associated with automation systems and control system software

Support engineering and validation projects as well as provide support to manufacturing activities with process control and process monitoring equipment software design, commissioning, and testing to meet end user requirements

Supporting automation activities by updating/authoring system specifications, user and functional requirements specifications, as well as generating and implementing necessary FAT and SAT protocols

Designing and developing test plans and implementing software/hardware improvements to automated process control and process monitoring equipment according to change control procedures

Ensuring systems' data is backed up / archived as required to ensure system can meet defined RTO and RPO; perform recovery of data as needed

Creating and maintaining configuration specifications for cGMP software for process control, monitoring and testing

Ensuring systems remain in compliant state including process change control requests for system configurations, including requirement and/or design specifications, test plans, technical evaluation and quality risk assessments

Supporting system integration with existing systems (ex. LIMS, Historian) as required by business needs

This role might be for you if you:

You enjoy working in a fast-paced environment and can be flexible with changing priorities

You thrive in a team-based, multi-functional, collaborative environment

You possess a problem-solving mentality

You have excellent verbal and written communication skills

In order to be considered for this role,you must have at least a Bachelor's degree in Information Technology or related field and 3-5 years of relevant experience in a manufacturing/lab/IT setting. Must have experience in a pharmaceutical or biopharmaceutical manufacturing facility. Must have experience with automated systems for environmental monitoring and compliance; Rees is preferred. Experience working in a GMP environment is very advantageous.

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