Shaping the digital future of life sciences with up to data!
For more than 30 years, we have been a trusted partner for pioneering digital solutions for laboratory management and reporting. As a driver of innovation, we help leading companies in the life sciences, pharmaceutical, chemical and biotech industries optimize their processes with cutting-edge IT applications.
We are a team of specialists who are passionate about driving digital transformation in the pharmaceutical industry. Our core competency is the digitization of study data processing for regulatory submissions - an area in which we aim to set new IT standards.
At up to data, we foster an environment where creativity and innovation can flourish. Through exciting digitization projects, we grow together and make a meaningful contribution to improving the quality of life for people around the world.
For the successful launch of our innovative software platform StudyGen 360, we are looking for an experienced
Your Impact
As Technical Project Manager, you'll be the driving force behind our software development projects, expertly bridging technical innovation, regulatory requirements, and customer expectations. Working closely with our R&D team, you'll lead the evolution of StudyGen's capabilities while ensuring compliance with pharmaceutical industry standards.
Key Responsibilities
Software Development Leadership:
- Lead technical development of StudyGen platform in complex enterprise projects
- Coordinate with R&D to define and implement new features and architectural improvements
- Manage full software development lifecycle in a regulated environment
- Guide technical decision-making processes and architecture evolution
- Ensure compliance with GxP regulations and industry standards
Project Management Excellence:
- Drive enterprise-level implementation projects for pharmaceutical clients
- Create and maintain project plans, timelines, and resource allocation
- Monitor project risks and implement mitigation strategies
- Coordinate between development teams, product management, and stakeholders
Requirements
Technical Expertise:
- Comprehensive understanding of modern software architecture and cloud technologies
- Strong development background in C#, JavaScript (React), and Razor
- Solid grasp of software testing methodologies and quality assurance
- Knowledge of agile development practices and tools
- Experience with regulatory requirements in pharmaceutical software development
Professional Experience:
- Minimum 2 years experience in technical project management of software development
- Experience with formal project management methodologies
- Experience leading development teams in enterprise software projects
- Understanding of GxP compliance and validation requirements
Personal Skills:
- Exceptional communication abilities with technical and non-technical stakeholders
- Analytical thinking and problem-solving skills
- Ability to manage multiple priorities in a fast-paced environment
- Excellent English skills, both written and verbal (German is a plus)
Benefits
- Opportunity to shape pharmaceutical software development in a growing company
- Work with cutting-edge technologies in challenging enterprise projects
- Competitive salary package
- Flexible work arrangements with modern office facilities
- International project exposure and networking possibilities
- Modern work environment with latest tools and technologies
- Regular team events and knowledge sharing sessions
- 28 days annual leave with flexible scheduling options
Ready to Take on This Exciting Challenge?
If you're passionate about leading technical innovation in pharmaceutical software and ready to drive complex enterprise projects to success, we want to hear from you. Join us in shaping the future of bioanalytical research through technology.
Apply now with your CV and a brief cover letter explaining why you would be the perfect fit for this role.
