Validation Engineer 1 jobs in United States
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Ecocareers ยท 3 months ago

Validation Engineer 1

Confidential company is seeking a Senior Validation Engineer to support digital initiatives within the Bioanalytical and Molecular Assays department of CASL. The role involves enhancing data integrity solutions and integrating systems to achieve efficient data delivery for metabolomic and genomic platforms.

Staffing & Recruiting

Responsibilities

Client is seeking a Senior Validation Engineer to support digital initiatives within the Bioanalytical and Molecular Assays department of CASL
This role will report directly to the Senior Manager of Operations and will be responsible for delivery of efficiencies to the Watson LIMS database, along with establishment of robust data integrity solutions for metabolomic and genomic platforms
Partner with Operations team to support Data Integrity Risk Assessment (DIRA) initiative, which will summarize potential risks and identify gaps in validated data-generating systems
Work toward achievement of a seamless sample-receipt-to-data-delivery model by integrating shipment manifests and EDC with Watson LIMS, and by leveraging custom reporting features of Watson LIMS
Introduce/coordinate metabolomic capabilities for LC-MS team by: Authoring Risk Assessment and partial User Test Cases for the high-resolution Orbitrap platform
Introduce/coordinate NGS (exosome-profiling) for molecular team by: Authoring Risk Assessment and partial User Test Cases for the Illumina NextSeq2000 platform
Represent BMA for data storage and movement solutions within client AWS cloud environment to achieve data integrity for large metabolomic and genomic datasets

Qualification

Computer Systems ValidationWatson LIMSKneatVeevaServiceNowChange ControlContinuous ImprovementDeviationsCommunication skillsTeam collaboration

Required

Master's degree in engineering or related field or relevant experience; a combination of education and experience may be considered
5 - 8 years of experience working in a regulated (GLP/GCLP/GMP) Pharmaceutical/Biotechnology environment
Strong understanding of Computer Systems Validations and instrument lifecycle processes
Subject Matter Expert in Watson LIMS
Understanding of the principles surrounding data integrity and digital compliance
Proficiency in Kneat, Veeva, and ServiceNow
Experience with Change Control, Continuous Improvement, and Deviations

Preferred

Strong communication skills (verbal and written)
Demonstrated ability to work independently and collaboratively on cross-functional teams
A desire to make an impact as part of a high-growth, transformational company that is Bold, Relentless, Curious, and Collaborative

Company

Ecocareers

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Funding

Current Stage
Early Stage
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