MIGx is a general consulting company with an exclusive focus on the healthcare and life science industries, with their particularly demanding requirements on quality and regulatory aspects. We have been managing challenges and solving problems for our clients in the areas of compliance, business processes and many others.

MIGx interdisciplinary teams from Switzerland, Spain and Georgia have been taking care of projects in the fields of M&A;, Integration, Application, Data Platforms, Processes, IT management, Digital transformation, Managed services and compliance.

Project Description Our company is rapidly growing and now we are looking for a Business Analyst/Life Sciences Consultant with a Life Science / Pharma R&D; focus to join our team of professionals. For this role you should have a minimum of 3 years of experience in a relevant business analyst, technical, scientific or SME role within the pharmaceutical or biotech industry.

Join MIGx as a Business Analyst/Life Sciences Consultant and help shape the future of pharmaceutical R&D.; Work with global teams to drive digital transformation and data excellence in life sciences.

Responsibilities

Work closely with cross-functional teams to gather and analyze business requirements

Create technical specifications and other documentation

Product Owner and/or Product Manager experience (PB mgt, definition of Features, US, etc.)

Analyze and model complex process/data flows to support pharmaceutical R&D; or CMC initiatives

Support system implementation, integration, data quality initiatives and validation efforts

Participate in requirement workshops and User Acceptance Testing





Using subject matter expertise to support and guide internal teams

Act as a trusted advisor to clients, offering insights on digital transformation in life sciences

Participate in workshops, gap analyses, and process improvement initiatives.

Requirements - Must have

Experience with drug development lifecycle, clinical trials, regulatory requirements, manufacturing (e.g., GxP, FDA, EMA)

Subject matter expertise in an area of Pharmaceutical R&D; or CMC

Experience with data modeling, requirements engineering, and process mapping

Familiarity with Pharma R&D; systems (e.g., CDMS, CTMS, PV, RIM, LIMS, ELN, or eTMF systems)

Proficiency in data visualization tools like Power BI, Tableau, Spotfire

Requirements - Nice to have

Experience with data lifecycle management, metadata strategy, and data stewardship

Familiarity with any of biostatistics, bioinformatics, clinical data, research data, RWD or lab informatics

Experience of CMC processes (e.g. product stability validation, batch tracing) and systems

Knowledge of data standards (e.g., CDISC, HL7, IDMP) and data governance

Proficiency in a programming language like R, SAS or Python

Experience with requirements management tools (e.g., Jama, DOORS) and Software Development Lifecycle instruments (e.g., Jira, Azure DevOps)

Understanding of “Data as a Product” principles and data product ownership

Experience with Data Mesh, graph databases, and ontology development to support next-gen data architectures

Experience with Data Modeling: Relational, Dimensional, Graph

Experience with data-focused solutions in the cloud e.g. Azure: Synapse, Databricks

📌 Business Analyst / Life Sciences Consultant (Madrid)
🏢 MIGx
📍 Madrid