PbAbout the profile /b /ppbAbout MIGx /b /ppMIGx is a global 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. /p pMIGx interdisciplinary teams from Switzerland, Spain and Georgia have been taking care of projects in the fields of MA, Integration, Application, Data Platforms, Processes, IT management, Digital transformation, Managed services and compliance. /p pbProject Description /b /ppOur company is rapidly growing and now we are looking for a Business Analyst/Life Sciences Consultant with a Life Science / Pharma RD 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. /p pJoin MIGx as a Business Analyst/Life Sciences Consultant and help shape the future of pharmaceutical RD. Work with global teams to drive digital transformation and data excellence in life sciences. /ppbr/ppbResponsibilities /b /ppbr/pulliWork closely with cross-functional teams to gather and analyze business requirements /liliCreate technical specifications and other documentation /liliProduct Owner and/or Product Manager experience (PB mgt, definition of Features, US, etc.) /liliAnalyze and model complex process/data flows to support pharmaceutical RD or CMC initiatives /liliSupport system implementation, integration, data quality initiatives and validation efforts /liliParticipate in requirement workshops and User Acceptance Testing /liliUsing subject matter expertise to support and guide internal teams /liliAct as a trusted advisor to clients, offering insights on digital transformation in life sciences /liliParticipate in workshops, gap analyses, and process improvement initiatives. /li /ulpbr/ppbRequirements - Must have /b /ppbr/pulliExperience with drug development lifecycle, clinical trials, regulatory requirements, manufacturing (e.g., GxP, FDA, EMA) /liliSubject matter expertise in an area of Pharmaceutical RD or CMC /liliExperience with data modeling, requirements engineering, and process mapping /liliFamiliarity with Pharma RD systems (e.g., CDMS, CTMS, PV, RIM, LIMS, ELN, or eTMF systems) /liliProficiency in data visualization tools like Power BI, Tableau, Spotfire /li /ulpbr/ppbRequirements - Nice to have /b /ppbr/pulliExperience with data lifecycle management, metadata strategy, and data stewardship /liliFamiliarity with any of biostatistics, bioinformatics, clinical data, research data, RWD or lab informatics /liliExperience of CMC processes (e.g. product stability validation, batch tracing) and systems /liliKnowledge of data standards (e.g., CDISC, HL7, IDMP) and data governance /liliProficiency in a programming language like R, SAS or Python /liliExperience with requirements management tools (e.g., Jama, DOORS) and Software Development Lifecycle instruments (e.g., Jira, Azure DevOps) /liliUnderstanding of “Data as a Product” principles and data product ownership /liliExperience with Data Mesh, graph databases, and ontology development to support next-gen data architectures /liliExperience with Data Modeling: Relational, Dimensional, Graph /liliExperience with data-focused solutions in the cloud e.g. Azure: Synapse, Databricks /li /ul