Strategy & Consulting - Global Network - Industry X - LabVantage LIMS

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We are looking for professionals with previous experience working with LabVantage LIMS at the Pharmaceutical industry, to join our team and work with global clients.

We have openings for Solutions Architects, Business Analysts and CSV Leads.

As a Solutions Architect you will be responsible for designing, developing, and implementing LIMS solutions that optimize laboratory operations and integrate seamlessly with various data management systems. Key Responsibilities: Design and Architecture, Solution Implementation & Integration, Stakeholder Collaboration, Technical Leadership, Documentation & Compliance, Support and Optimization, among others.

As a Business Analyst, you will assist in defining, developing, and validating requirements and LabVantage LIMS applications/interfaces to meet business processes and application requirements. Main responsibilities: Develop Validation Plans and Change Controls for LabVantage LIMS, develop Validation testing strategy, work closely with other teams to implement LIMS projects effectively and efficiently, assist with understanding the business requirements, analyze and help translate into functional requirements for assigned LIMS projects, among others.
 

As a Validation Lead (CSV) you have to come up with creative solutions to problems, clearly communicating your solutions, mostly in the form of visual models, wireframes, prototypes, and interfaces. Main responsibilities: coordinating validation activities for the respective system, setting up the validation approach for the project as per the applicable regulations, procedures, and guidelines, project planning, produce high-quality designs to prototype, test, evaluate and demonstrate interactions with customers, stakeholders, and developers, among others.

• Bachelor’s or Master’s degree in Computer Science, Information Systems, Life Sciences, or related field.

• Fluency in English is a must.

• Deep understanding of pharmaceutical laboratory regulatory constraints and process.

• Experience with LabVantage LIMS.

• Experience in clinical, pharmaceutical, and/or manufacturing industries.

• Experience with FDA, ISO, GxP, and HIPAA regulations is a plus.

• Availability to travel may be required

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