NNIT

Principal Consultant – Regulatory Affairs

Fès-Meknès

CDI / Temps pleinHybrideLicence / Bac+3Anglais, Allemand, Italien, FrançaisPharmaceutique

L’essentiel du poste

Résumé par Postule AI

Principal Consultant role at NNIT, a leading life sciences consultancy, combining 60% project delivery in Regulatory Affairs with 40% business development, strategy, and team leadership. Requires 10+ years of regulatory affairs experience in pharma/consulting, strong sales acumen, and senior-level consulting credentials. Based in Europe with travel up to 10%.

Vos missions

  • Deliver consultancy projects as advisor, project lead, or architect (60% of time)
  • Drive business development, presales, and thought leadership initiatives (20%)
  • Develop commercial offerings, methodologies, and consultant training materials (10%)
  • Develop and deliver RFPs to secure new client engagements (5%)
  • Coach and mentor consultants at all levels in Regulatory Affairs (5%)

Profil recherché

  • You have 10+ years of regulatory affairs experience in pharma or consulting
  • You combine strong technical expertise with sales and business development skills
  • You thrive in senior leadership roles mentoring teams on complex projects
  • You are fluent in English and interested in European-based opportunities
  • You have experience with RIM systems, IDMP, or Master Data Management

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About the Role

Join NNIT's Regulatory Affairs team as a Principal Consultant, leading strategy development and execution for our growing business unit. This is a senior leadership position combining consulting delivery, business development, and team mentorship within the life sciences industry.

Key Responsibilities

  • Deliver consultancy projects (60%) in advisor, project lead, or architect roles, acting as engagement delivery lead
  • Drive business development, presales, and thought leadership activities (20%)
  • Develop consultancy commercial offerings, delivery methodologies, and training materials (10%)
  • Develop and deliver Requests for Proposal (RFP's) to secure new projects (5%)
  • Coach and mentor consultants across all levels in the Regulatory Affairs team (5%)

Essential Requirements

  • Bachelor's Degree in Pharmaceutical Compliance, Regulation, or related field with significant Regulatory Affairs experience in pharmaceutical companies or consulting
  • Proven consulting experience, ideally within a large recognized consultancy with life sciences specialization
  • Strong sales and business development aptitude in a consulting environment
  • Experience managing client, partner, and vendor interactions
  • Excellent documentation, communication, and interpersonal skills

Preferred Qualifications

  • Master's level qualification in Pharmaceutical Compliance or Regulation
  • Deep MedTech and BioTech industry or consulting experience
  • RIM systems, IDMP, and Master Data Management experience
  • Experience bringing new products to market
  • People management and project leadership on complex, multi-stakeholder projects

What We Offer

  • Dynamic workplace with excellent working conditions, social activities, and work-life balance
  • Multicultural, friendly environment with significant life sciences clients
  • Competitive salary, bonus, and benefits (home internet contribution, fitness funding)
  • Career development model and diverse project opportunities
  • Travel limited to necessary business trips (<10%)

Location & Languages

European positions available in UK, Denmark, Germany, Ireland, Italy, Poland, Spain, or other European locations. Fluency in English (required); German, Danish, Italian, or French (desired).

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