Veracity Software Inc
Master Data Specialist
Veracity Software Inc - Trenton, New Jersey, United States
Work at Veracity Software Inc
Overview
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Overview
**12 Months Contract**
50/50 hybrid role, 3 days onsite one week, 2 days onsite the next.
Responsible for the creation and execution of computer system validation documents, as well as providing operational support and guidance related to system use and improvement.
Duties/Responsibilities
Create and execute computer system validation documents (i.e., UAT, URS, OQ, PQ, etc.) as applicable and guide QC end users on the development of system enhancements with user requirements and business drivers.
Provide electronic systems operational support and troubleshooting to end users.
Create, deploy, review, and maintain electronic systems Master Data. Perform data verification, system integration (LIMS, ERP, and MES) for electronic systems.
Own project, CAPA, and deviation/investigation related tasks and/or continuous improvement efforts.
Propose and implement improvements to electronic systems to optimize business processes and improve efficiency. Collaborate with end users to develop business cases.
Support strategic initiatives by anticipating mid- to long-term business needs and constraints.
Perform troubleshooting and problem solving independently.
Train and mentor others on electronic systems use and operation.
Translate business requirements into technical design requirements and communicate with partner organizations (e.g., IT) for system solutions.
Facilitate design, testing, and deployment of solutions.
Support health agency inspections as equipment area subject matter expert.
Perform other tasks as required to support electronic systems.
Reporting Relationship This position will report to QC management.
Knowledge, Skills, Abilities
Understanding, following, interpreting, and applying Global Regulatory and cGMP requirements.
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Advanced technical, problem-solving skills, and logical thinking.
Effective communication with peers, management, and cross-functional teams.
Mentoring, coaching, influencing, negotiating, and personnel interaction skills.
Education/Experience/Certifications
Bachelor's degree in science or related engineering field.
6+ years of relevant experience with LIMS, ELN, and laboratory data analysis systems, preferably in a regulated environment.
Experience with validation and maintenance of laboratory information systems.
Knowledge of analytical and microbiological test methods and environmental monitoring programs (preferred).
Technical writing skills.
Seniority level Mid-Senior level
Employment type Full-time
Job function Other
Industries IT Services and IT Consulting
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50/50 hybrid role, 3 days onsite one week, 2 days onsite the next.
Responsible for the creation and execution of computer system validation documents, as well as providing operational support and guidance related to system use and improvement.
Duties/Responsibilities
Create and execute computer system validation documents (i.e., UAT, URS, OQ, PQ, etc.) as applicable and guide QC end users on the development of system enhancements with user requirements and business drivers.
Provide electronic systems operational support and troubleshooting to end users.
Create, deploy, review, and maintain electronic systems Master Data. Perform data verification, system integration (LIMS, ERP, and MES) for electronic systems.
Own project, CAPA, and deviation/investigation related tasks and/or continuous improvement efforts.
Propose and implement improvements to electronic systems to optimize business processes and improve efficiency. Collaborate with end users to develop business cases.
Support strategic initiatives by anticipating mid- to long-term business needs and constraints.
Perform troubleshooting and problem solving independently.
Train and mentor others on electronic systems use and operation.
Translate business requirements into technical design requirements and communicate with partner organizations (e.g., IT) for system solutions.
Facilitate design, testing, and deployment of solutions.
Support health agency inspections as equipment area subject matter expert.
Perform other tasks as required to support electronic systems.
Reporting Relationship This position will report to QC management.
Knowledge, Skills, Abilities
Understanding, following, interpreting, and applying Global Regulatory and cGMP requirements.
Ability to work in a fast-paced team environment, meet deadlines, and prioritize work.
Advanced technical, problem-solving skills, and logical thinking.
Effective communication with peers, management, and cross-functional teams.
Mentoring, coaching, influencing, negotiating, and personnel interaction skills.
Education/Experience/Certifications
Bachelor's degree in science or related engineering field.
6+ years of relevant experience with LIMS, ELN, and laboratory data analysis systems, preferably in a regulated environment.
Experience with validation and maintenance of laboratory information systems.
Knowledge of analytical and microbiological test methods and environmental monitoring programs (preferred).
Technical writing skills.
Seniority level Mid-Senior level
Employment type Full-time
Job function Other
Industries IT Services and IT Consulting
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