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About the Role
Develop innovative solutions in Strategy, Risk & Transactions – Advisory – Regulatory & Compliance. Shape the future of regulation by developing solutions for complex regulatory challenges for clients across various industries.
Responsibilities
- Advise clients in Pharma, Biotechnology, and Medical Technology on regulatory issues along the pharmaceutical value chain.
- Develop pragmatic and robust solutions for regulatory operating models, supply chain setups, and quality processes, especially in complex international constellations.
- Analyze and evaluate regulatory requirements in the GMP, GDP, and GxP environment and derive concrete courses of action for clients.
- Develop and evaluate EU and international operating models, including Wholesale Distribution Authorisation (WDA), Manufacturing & Import Authorisation (MIA), and the responsibilities of Responsible Person (RP) and Qualified Person (QP).
- Independently conduct gap assessments, risk analyses, and compliance reviews.
- Translate regulatory requirements into actionable processes, governance structures, and decision proposals.
- Take ownership of work packages in consulting projects, structure regulatory issues, and prepare results for management.
- Present and communicate findings effectively.
- Work in a structured manner with a high degree of responsibility for own work packages.
Requirements
- Successfully completed degree in Pharmacy, Natural Sciences, or another Life Sciences discipline with very good academic performance.
- Relevant professional experience of 3-5 years in the pharmaceutical industry, biotechnology, medical technology, or consulting, ideally with a focus on Regulatory Affairs, Quality, Supply Chain, or GxP Compliance.
- Sound knowledge of European GMP, GDP, and GxP requirements.
- Experience with WDA, MIA, QP/RP responsibilities, Quality Agreements, or regulatory operating and responsibility models is advantageous.
- Strong consulting skills in structuring, evaluating, and practically implementing complex regulatory requirements.
- Strong presentation and communication skills.
- Structured way of working and high sense of responsibility for own work packages.
- Willingness to travel.
- Very good German and English language skills.
Skills
- Regulatory Affairs
- Quality Assurance
- Supply Chain Management
- GxP Compliance
- GMP
- GDP
- WDA
- MIA
- QP/RP Responsibilities
- Quality Agreements
- Operating Models
- Risk Analysis
- Compliance Review
- Presentation Skills
- Communication Skills
- Project Management
Location
- Berlin
- Düsseldorf
- Munich
Work Type
- Full-time
- Hybrid
- Mobile Working
- EU Remote Working
Experience Level
- Senior Consultant
- 3-5 years of professional experience
Education Level
- Degree in Pharmacy, Natural Sciences, or another Life Sciences discipline
Benefits
- Best-in-class training at Deloitte University and individual qualification programs.
- Comprehensive development opportunities through structured career planning, inclusive leadership, secondment programs, project-based job rotation, and support for social engagement and corporate volunteering.
- Work-life balance through mobile working & part-time, sabbaticals, and family services.
- Health & fitness focus through regular health days, partnerships with fitness providers, and support for sports and team events.
- Attractive employer benefits including bike and car leasing, company smartphone for private use, and flexible working models like trust-based working hours and EU remote working.
- Diverse opportunities for contribution and active promotion of an inclusive corporate culture through employee networks.
About the Company
- Part of Strategy, Risk & Transactions – Advisory – Regulatory & Compliance.
- Works with clients across all industries including Finance, Public, Energy, Life Sciences, and Automotive.
- Develops solutions for complex regulatory challenges.
Equal Opportunity
- Equal opportunities for everyone, regardless of age, disability, ethnic origin and nationality, gender, religion, sexual orientation, or social origin.