BIOVIA ELN Developer
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Job Location:
Jersey, NJ - USA
Monthly Salary:
Not Disclosed
Posted on:
Yesterday
Vacancies:
1 Vacancy
Job Summary
Role Overview:
Experienced BIOVIA ELN Developer to design configure and implement Electronic Laboratory Notebook solutions for scientific R&D environments. The ideal candidate will have strong hands-on experience with BIOVIA ELN and related integrations ensuring compliance scalability and seamless collaboration across teams.
Key Responsibilities:
Configure and customize BIOVIA ELN workflows templates and protocols to meet business requirements.
Integrate ELN with other systems such as LIMS PLM ERP and scientific instruments.
Develop and maintain scripts APIs and connectors for data exchange.
Ensure compliance with GxP FDA 21 CFR Part 11 and other regulatory standards.
Troubleshoot and resolve technical issues related to ELN configuration and performance.
Collaborate with scientists IT and QA teams to gather requirements and deliver solutions.
Create and maintain documentation SOPs and operational guidelines.
Provide training and support to end-users and stakeholders.
Required Skills & Experience:
Strong hands-on experience with BIOVIA ELN configuration and customization.
Knowledge of scientific workflows and R&D processes in pharma/biotech or chemicals.
Experience with system integration (LIMS ERP instruments) and API development.
Familiarity with SQL scripting languages and web technologies.
Understanding of regulatory compliance (GxP Part 11).
Excellent problem-solving and communication skills.
Ability to work independently and in a collaborative environment.
Preferred Qualifications:
Experience with other BIOVIA products (Pipeline Pilot LIMS).
Relevant certifications in BIOVIA or ELN technologies.
Exposure to cloud-based deployments and security best practices
Experienced BIOVIA ELN Developer to design configure and implement Electronic Laboratory Notebook solutions for scientific R&D environments. The ideal candidate will have strong hands-on experience with BIOVIA ELN and related integrations ensuring compliance scalability and seamless collaboration across teams.
Key Responsibilities:
Configure and customize BIOVIA ELN workflows templates and protocols to meet business requirements.
Integrate ELN with other systems such as LIMS PLM ERP and scientific instruments.
Develop and maintain scripts APIs and connectors for data exchange.
Ensure compliance with GxP FDA 21 CFR Part 11 and other regulatory standards.
Troubleshoot and resolve technical issues related to ELN configuration and performance.
Collaborate with scientists IT and QA teams to gather requirements and deliver solutions.
Create and maintain documentation SOPs and operational guidelines.
Provide training and support to end-users and stakeholders.
Required Skills & Experience:
Strong hands-on experience with BIOVIA ELN configuration and customization.
Knowledge of scientific workflows and R&D processes in pharma/biotech or chemicals.
Experience with system integration (LIMS ERP instruments) and API development.
Familiarity with SQL scripting languages and web technologies.
Understanding of regulatory compliance (GxP Part 11).
Excellent problem-solving and communication skills.
Ability to work independently and in a collaborative environment.
Preferred Qualifications:
Experience with other BIOVIA products (Pipeline Pilot LIMS).
Relevant certifications in BIOVIA or ELN technologies.
Exposure to cloud-based deployments and security best practices
Key Skills
- CCTV
- Computer Science
- Corporate Marketing
- E Learning
- Arabic English Translation
