22 set - Follonica
NNIT
UK, Denmark, Italy, Germany, Poland, Czech, Ireland, SwitzerlandType of contract: PermanentTutti i potenziali candidati sono incoraggiati a leggere l'intera descrizione del lavoro prima di candidarsi.Location(s): UK, Denmark, Italy, Germany, Poland, Czech, Ireland, SwitzerlandLanguage(s): EnglishMobility: Some TravelApplication Deadline: 30/10/2026Senior Consultant - Regulatory AffairsNNIT is one of the world’s leading consultancies for the past twenty years serving the Life Science industry around the world. We strive to enable our customers to achieve their business goals through digitalization within Quality Assurance, Regulatory Affairs, Clinical, Pharma Production and Laboratory processes.Your ResponsibilitiesYou will join our Regulatory Affairs team as a Senior Consultant. You will contribute to forming a variety of tasks and functional responsibilities within the Regulatory Affairs business unit such as taking ownership of client engagements and specific projects, contribute to business development and sales activities and contribute to and deliver Requests for Proposal (RFP’s) as required.On Average You Will Split Your Time75% delivering in consultancy projects in advisor, project lead or architect roles, and acting as engagement delivery lead.10% in business development, presales and though leadership activities10% in the development and delivery of RFP’s to ensure NNIT successfully engages new and additional projects5% in coaching and mentoring of more junior consultants in the Regulatory Affairs teamEssential RequirementsYour qualifications and experience:A Bachelor’s Degree (or similar) in a field related to Pharmaceutical Compliance or Regulation. Other relevant academic qualifications can be considered if you also have highly significant consulting and/or industry based experience inRegulatory Affairs within Life Sciences.Significant experience in Regulatory Affairs within a Pharmaceutical company or as a consultant.Proven consulting based experience is an essential requirement for the role,
ideally within a large recognised consultancy with a life sciences division or specialism.A proven level of experience in the area of IDMP including some of the following:Experience in IDMP data transformationData enrichment for PMS, RIMS and XEVMPDExperience with RIM systems related to IDMPFully aware and cognizant of current EMA updates on IDMPExperience presenting IDMP topics to larger audiencesProficiency in PMS and Postman APIExperience in managing interactions with clients, partners and vendors and an interest in driving and expanding NNIT client relations as part of business development, pre-sales and project delivery activities.First class documentation, communication, and interpersonal skills, with an ability to liaise effectively and professionally with individuals at all levels.Preferred RequirementsA Masters level qualification in a relevant area of study such as Pharmaceutical Compliance or Regulation.Regulatory experience within the Pharmaceutical industry.Consulting experience within a recognised consulting firm.Experience working within Regulatory Affairs for a pharmaceutical company.Experience with Power BI application.Phyton coding and scripting experience.Why should you join NNIT & What we offer to you?A dynamic workplace with good working conditions, social activities, team events and work life balance.Opportunity to work in a multicultural company with a friendly and dynamic work environment.Competitive salary, additional bonus and agevolazioni package (contribution to your home internet, fitness funding, and others).An Informal and friendly working culture between NNIT colleagues.Opportunity to work with the most significant life sciences clients.Diversity of projects, and the possibility of shaping your own career path.Personal development model which defines your long-term career goals.We are hiring into our European team in the following countries: UK or EuropeFluency in oral and written English is a must. xysqume A second language (German, Danish, Italian or French) is desired but not essential.Travel must beexpected, but will be kept to necessary business trips (
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