Senior Digital Life Science Consultant- (Regulatory Affairs)
Pubblicato il 08-08-2026 - Productlife Group in Bardi
ph3Overview /h3 pLifeBee, is a ProductLife Group Company and leading international strategic and digital consulting firm, supporting Life Science companies in their journey towards digitalization, technological innovation, operational excellence, and proactive compliance.
The focus is on the GxP regulated areas of Chemical, Bio-Pharmaceutical, Medical Devices, and Nutraceutical companies, particularly in Production, Quality Assurance, Laboratories, Logistics, Serialization, Industrial Operations, Regulatory Affairs, and Pharmacovigilance.
ProductLife Group (PLG) is a dedicated life sciences outsourcing and consulting company.
The group has its HQ in Paris and affiliates around the globe with teams in all key regions: North America, Europe and APAC.
If you are passionate about Digital Transformation and Life Sciences and are keen to make an impact and lead international high?profile customers through their digitalisation journey, you have read!
/p h3Your Role /h3 pAccording to your experience and expertise, you will have the ownership of and be responsible for increasingly complex activities aimed at the successful delivery of numerous projects, supporting both local and international clients in the Pharmaceutical and Life Sciences sector.
/p h3Responsibilities /h3 ul liAdvising customers, through frequent and close interaction, in analysing and designing the most suitable solutions to their needs so as to help them achieve their goals.
/li liImplementing, customizing and integrating market?leading and cutting?edge software applications for Life Sciences.
/li liPlanning and executing project streams, drafting specifications, tests and validation technical documentation.
/li liEnhancing close collaboration with local and global software vendors.
/li liProviding added value to our customers, through qualified technical and functional support and training.
/li liOverseeing and supporting technical validation activities.
/li /ul h3Qualifications /h3 ul liSTEM degree preferred (e.g., computer science, bioinformatics, computer engineering, biomedical engineering, mathematical engineering, statistics, physics).
/li li2 years of relevant experience (or more) gained in a Consultant role.
/li liKnowledge of IT systems, coding languages, and MS Office productivity tools.
/li liKnowledge of Life Sciences Software solutions, regulations and guidelines.
/li liAnalytical and problem solving approach.
/li liFluency in Italian and English is required.
/li /ul h3Nice to Have /h3 ul liKnowledge of programming languages (e.g., SQL, Javascript, Python, C#).
/li liKnowledge of Industry (preferred in Life Science Market) Software Solution, particularly in RIMs, QMS, MES/EBR, BPM, LIMS, Workflow Management, Document Management, Business Analytics, Machine Learning, Artificial Intelligence.
/li liKnowledge of Regulatory software solutions such as Veeva RIMS (modules: Submissions, Submissions Archive Registrations), Extedo RIMS ("Pulse"), Aris Global RIMS, Ennov.
/li /ul h3Benefits /h3 ul liFull?time permanent employment contract.
/li liHybrid working policy.
/li liContinuous technical and professional development training.
/li liBenefits package (welfare, private health insurance).
/li liMeal vouchers.
/li liExcellent internal growth opportunities.
/li liCompetitive salary.
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