Regulatory Specialist managing site activation and compliance for clinical trials at IQVIA. Responsible for regulatory documents and project timelines ensuring adherence to operational procedures.
MA
Hybrid Senior Consultant – Governance, Risk & Compliance
Posted 4 months ago
About the role
- Leading consultant for governance, risk & compliance in IT and quality management. Working in projects in the manufacturing industry with a hybrid model in Germany.
Responsibilities
- Lead or sub-project lead in projects related to quality management and IT in the manufacturing industry
- Validation of IT systems in the areas of enterprise, customer, production and quality management
- Planning and execution of internal and external audits as well as gap analyses
- Ensuring collaboration between quality control, quality assurance and IT
- Active participation in acquisition processes and development of focus areas in IT compliance
Requirements
- Degree in engineering, computer science, medical informatics, natural sciences, or an equivalent qualification
- Experience in project management
- Solid understanding of regulatory requirements in the pharmaceutical industry
- Analytical and conceptual thinking
- Strong industry knowledge and a solution-oriented approach
- Confident communication in German and English
- Flexibility for remote work and on-site assignments
Benefits
- 30 days of annual leave and additional days off for special occasions
- Time value account for extended time off
- Internal training curriculum and supplementary learning formats
- Buddy program and internal networks
- Subsidized Urban Sports Club membership
- Exclusive discounts through Corporate Benefits
- Flexible mobility options (JobRad/company bike, company car or BahnCard)
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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