Lims Business Analyst

6 months ago


Montréal, Canada CellCarta Full time

**LIMS Business Analyst**

**Summary**

**Main Responsibilities**
- Collaborating with lab operations to develop and execute user acceptance tests for business requirements
- Collaborating with IT to design and prepare adequate user requirements, functional and technical documentation
- Provides training and developing user guides
- Drafts user and functional requirements and user stories documentation
- Drafts, reviews and updates SOPs
- End user training support
- Analyze business processes and summarize them in both visual and written formats
- Gather business requirements and support the business in the definition of correct requirements to meet business needs
- Prepare functional requirements documentation Performing business / functional testing in agile sprints
- Provides business and IT teams thought leadership and guidance in developing realistic project plans, resource plans, cutover and deployment plans, data migration plans
- Writing and reviewing general SOPs, in collaboration with stakeholders across sites as needed to ensure harmonization of processes
- Harmonized global processes and master data structures
- Application capabilities optimization based on configurable capabilities, vendor supportable solutions as a goal, customization as a last resort
- End to end global process-based solutions

**Education**
- B.S.c. Sciences, or MSc. Sciences in biomedical sciences or a related field combined with hands-on lab experience with multiparametric flow cytometry

**Main Requirements**
- Analytical mindset, capable of understanding complex problems, abstracting and representing them in a structured way
- 2+ years CRO or pharma industry experience, with a Laboratory Information Management System (StarLIMS experience ideal)
- Previous laboratory and training experience in a Contract Research Organization (CRO), clinical lab or pharma, operating to Good Laboratory Practice (GLP) standards
- Previous experience in Lab Application development, validation, testing and implementation an important asset
- Excellent communication, organizational and leadership skills
- Excellent knowledge and experience working in a GLP/GCLP environment
- Attention to detail
- Professional level of English: spoken and written to ensure clear communication with staff members
- Ability to coordinate, manage and complete tasks and projects with mínimal oversight
- Ability to multitask over multiple projects
- Capable of collaborating with teams both cross-functionally and remotely, across a wide range of time zones and cultures
- Possesses the behavioral attributes of the competencies in the CellCarta competency model: critical thinking and analysis, business insight, decision making, drive for results, operational expertise, project management and process improvement, people management, collaboration and teamwork
- General computer skills: Word, Excel, PowerPoint and Outlook
- Experience in project managing tools such as Jira is a plus

**Working Conditions**
- Employee must follow company safety precautions in the conduct of their work and follow SOPs at all times.
- Teleworking is acceptable, but occasionally (up to a couple days a week), presence on-site will be required to have a better communication line with the CellCarta laboratories.
- Occasionally, work schedule may be adapted to accommodate business needs, especially when collaboration between sites is needed.

**Benefits**

We offer a wide range of benefits including:

- Competitive Wages;
- Vacation and Personal Days;
- Comprehensive Group Insurance Plans;
- RRSP Contribution with Employer Matching;
- Employee Annual Incentive Plan (EAIP);
- Dialogue Telemedicine Service and Employee Assistance Program (EAP);
- OPUS & Cie Contribution;
- Parking Reimbursement;
- Referral Program;
- Career advancement opportunities.

**About CellCarta**

CellCarta is a leading provider of specialized precision medicine laboratory services to the biopharmaceutical industry. Leveraging its integrated analytical platforms in immunology, histopathology, proteomics, and genomics, as well as related specimen collection and logistics services, CellCarta supports the entire drug development cycle, from discovery to late-stage clinical trials. The Company operates globally with facilities located in Canada, USA, Belgium, Australia, and China.

Joining CellCarta means working with dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world

**Join us as we make an impact on patient therapy**

9rGsjhUPDa



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