Hours: 37.5 hours per week
Business Unit: Diagnostics
Open To: Internal and external Applicants
Ref No.: HRJOB10364/1
The Role
Our Informatics team works closely with our internal operational testing teams and partners to provide efficient, customized, and innovative data capture and return solutions that meet their requirements for program-related data.
We are currently seeking an Informatics Developer to join our expert team. The role focuses on customizing data management systems like LIMS to meet reporting needs, generating SQL queries, and formatting and validating data. It involves supporting data reconciliation, returns, and archival, while ensuring secure electronic data storage. Responsibilities include following clinical laboratory practices, participating in data management training, ensuring data quality, and generating change requests for documentation and computerized systems. The role also encompasses supporting archival processes as an Electronic Data Archivist.
Key Requirements
Applicants must have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full-time employment in the UK.
1. Educated to at least a bachelor's degree level (or equivalent) in bioinformatics, computer science or a related discipline.
2. Demonstrable computation and software development skills.
3. Proficient coding skills in one or more scripting languages (Python, R, Bash, Groovy, etc.).
4. Proficient database administration and query design skills (e.g. SQL/PL-SQL, MySQL, Oracle).
5. Working knowledge of Server Operating Systems (Windows/Linux).
6. Knowledge of the key stages of system implementation lifecycle (requirements, design, development, testing).
(The following criteria may be applied if a large pool of applicants exist)
1. MSc (or equivalent) in bioinformatics, computer science or a related discipline.
2. Commercial experience within a data management role in a biotechnology or pharmaceutical company.
3. Familiarity with genomics and computational biology.
4. Experience designing & developing FDA or CE-Mark certified software solutions to support clinical assay delivery.
5. Previous experience working within a quality system and/or regulatory experience/knowledge (e.g. CFR part 11, Data Integrity best practices).
6. Experience with systems integration/middleware.
7. Experience using or customizing a LIMS system.
Apply Now
Apply online and tailor your CV to outline how you meet the role criteria. Please upload your CV in PDF format where possible.
Closing Date: We will no longer be accepting applications after 5pm on Sunday 13 April 2025.
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