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Regulatory Affairs Manager
2 weeks ago
Take on the role of Regulatory Affairs Manager at CIM A/S, where you'll focus on ensuring our software solutions meet the strict regulatory standards of the pharmaceutical industry.
About Our Company
CIM A/S is a pioneering company providing cutting-edge software solutions to the global pharmaceutical industry. Our comprehensive suite includes standard and custom solutions for data collection, decision support, traceability, digital print, vision inspection, and automated testing.
Your Job Summary
As a Regulatory Affairs Manager, you'll lead cross-functional teams to develop and implement regulatory-compliant software solutions that meet customer expectations.
Main Responsibilities
- Drive project execution, ensuring compliance with regulatory demands and customer requirements.
- Collaborate with project managers, software developers, and customer validation teams to deliver high-quality solutions.
- Support the creation and maintenance of validation documentation for software products.
Key Skills and Qualifications
- Hold a degree in a technical field and have a strong interest in technology.
- Possess experience with the validation process and knowledge of regulatory requirements.
- Familiarity with technical project delivery methodologies.
Why Join Us?
We offer a dynamic work environment with flexible schedules, allowing you to achieve a healthy work-life balance. Our office locations in Aarhus and Hørsholm provide ample opportunities for collaboration and growth.
Core Values
- Credibility and commitment to excellence.
- A systematic approach to work, combined with attention to detail.
- Exceptional communication skills and fluency in English.
- Ability to effectively interact with diverse stakeholders and navigate complex situations.
- A collaborative mindset and active participation in team growth.
Equal Employment Opportunity
CIM A/S welcomes applications from all qualified individuals, regardless of their background, age, gender, religion, or ethnicity.