At a Glance
- Tasks: Lead IT projects in R&D and ensure compliance with global regulations.
- Company: Viatris is a global healthcare company dedicated to empowering healthier lives.
- Benefits: Enjoy competitive salaries, career progression, and a diverse, inclusive work environment.
- Why this job: Make a real impact in healthcare while working in a collaborative culture.
- Qualifications: Bachelor's degree in IT or science; experience in pharma and Veeva systems preferred.
- Other info: Diversity and sustainability are core values at Viatris.
The predicted salary is between 48000 - 72000 £ per year.
At VIATRIS, we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs. Viatris empowers people worldwide to live healthier at every stage of life.
We do so via:
- Access – Providing high quality trusted medicines regardless of geography or circumstance;
- Leadership – Advancing sustainable operations and innovative solutions to improve patient health;
- Partnership – Leveraging our collective expertise to connect people to products and services.
Our global portfolio includes best-in-class, iconic brand-name products as well as global key brands; generics, including branded and complex generics; and other offerings across a wide range of therapeutic areas. We are committed to helping create healthier communities worldwide through education, outreach and better access to treatment.
For those driven to live their lives with purpose, Viatris helps employees realise their full potential by creating a collaborative culture that fosters courage and resilience. Viatris is more than just a place to work. This is a place to make a difference in the world.
The R&D and Regulatory Systems Manager position works with business partners in CMC, Regulatory Affairs, Medical Devices and other R&D functions to understand technology needs, ensure global processes and systems are compliant and representative of cross functional business needs. The successful candidate will demonstrate strong global CMC and Regulatory domain expertise, have hands on business analysis & IT project management experience including detailed requirements elicitation. Successful candidate will bring knowledge of configuring, integrating, and migrating Veeva RIM Registrations and Submissions Vaults.
Every day, we rise to the challenge to make a difference and here’s how the Manager, IT, R&D & Regulatory Systems role will make an impact:
- Provide strong working knowledge of the digital capabilities used to support global R&D business processes.
- Understand CMC, medical devices and regulatory processes and identify health authority trends and policies that could impact current systems.
- Monitor emerging global health authority requirements to assess business and system impact including developing and implementing requirements to ensure compliance.
- Collaborate with key business users to identify business needs and translate these needs to user requirements. Translate user requirements into technical requirements and implement solutions to meet requirements.
- Provide business analysis techniques including business and functional requirements gathering, process modeling, interviewing, user stories, prototyping, data flows, and root cause analysis.
- Successfully manage IT projects for R&D to implementation by coordinating activities of project personnel to ensure the project successfully delivers in scope, on schedule and within budget.
- Support project execution tasks to configure, integrate and migrate Veeva RIM Registrations and Submissions Vaults.
- Work with teams globally for end-to-end implementation of various R&D systems and ensure compliance with regulations by FDA, EMA and other health agencies.
- Drive compliance with IT Quality processes and Viatris SDLC processes, including IT change management and quality/testing procedures.
- Collaborate with solutions lead and business partners to ensure technologies are meeting business requirements.
- Support the vendor relationship for assigned R&D systems, ensuring that system issues are promptly communicated.
For this role, we’re looking for a candidate who has an effective combination of the following qualifications, skills and experiences:
- Bachelor's degree in a science, IT, or a relatable field. Advanced degrees are a plus.
- Prior experience in the pharmaceutical industry and a strong understanding of global R&D CMC, Medical Devices & Regulatory Affairs business processes.
- Experience with validated GxP environments, including Implementation, documentation, and Change Management is necessary.
- Hands on experience implementing, configuring and integrating Veeva Vault RIM platform including Registration, Submissions & Archive Vaults. Veeva certification desired.
- Broad technical knowledge, including experience with SaaS in a regulated environment.
- Experience in business processes for CMC, medical devices and for regulatory submission planning and tracking, registration management, commitment management and content management.
- Strong business analysis and project management skills as well as attention to detail.
- Ability to operate in a dynamic challenging environment and manage multiple activities, priorities, and deadlines.
- Excellent verbal and written communication skills.
- Works well in and appreciates the value of a global diverse work environment.
- Is able to see the larger picture and able to identify and successfully communicate key issues in complex situations.
At Viatris, we are dedicated to building a truly diverse, inclusive and authentic workplace, so if you’re excited about this role but your past experience doesn’t fully align with every requirement, we still encourage you to apply. You may just be the right candidate for this or other roles.
At Viatris, we offer competitive salaries, benefits and an inclusive environment where you can use your experiences, perspectives and skills to help make an impact on the lives of others. You will also have the opportunity to access excellent career progression opportunities and work-life balance initiatives.
Diversity & Inclusion at Viatris: At Viatris, diversity and inclusion are essential to our mission. The diversity we foster in all aspects of our business can be one of our greatest strengths in redefining healthcare not as it is, but as it should be.
Sustainability at Viatris: Corporate social responsibility is fundamental to the Viatris mission. We work to advance responsible and sustainable operations and leverage our collective expertise to empower people to live healthier at every stage of life, recognizing that our actions affect the stakeholders and communities we serve.
Viatris is an Equal Opportunity Employer.
Manager, IT, R&D & Regulatory Systems employer: Viatris
Contact Detail:
Viatris Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Manager, IT, R&D & Regulatory Systems
✨Tip Number 1
Familiarise yourself with Veeva Vault RIM platform, as hands-on experience with this system is crucial for the role. Consider taking online courses or certifications related to Veeva to demonstrate your commitment and knowledge.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who work in R&D and regulatory affairs. Attend industry conferences or webinars to connect with potential colleagues and learn about current trends and challenges.
✨Tip Number 3
Brush up on your project management skills, particularly in IT contexts. Familiarity with methodologies like Agile or Waterfall can be beneficial, so consider obtaining a relevant certification to enhance your profile.
✨Tip Number 4
Stay updated on global health authority regulations and trends that impact R&D processes. Subscribe to industry newsletters or follow relevant organisations on social media to keep your knowledge current and show your proactive approach during interviews.
We think you need these skills to ace Manager, IT, R&D & Regulatory Systems
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in IT project management, business analysis, and knowledge of regulatory systems. Use keywords from the job description to demonstrate your fit for the role.
Craft a Compelling Cover Letter: In your cover letter, express your passion for healthcare and how your skills align with Viatris' mission. Mention specific experiences that showcase your expertise in CMC, medical devices, and regulatory affairs.
Showcase Relevant Skills: Emphasise your hands-on experience with Veeva Vault RIM platform and any certifications you hold. Highlight your ability to manage multiple projects and your strong communication skills, as these are crucial for the role.
Proofread and Edit: Before submitting your application, carefully proofread your documents for any spelling or grammatical errors. A polished application reflects your attention to detail and professionalism.
How to prepare for a job interview at Viatris
✨Understand the Role Thoroughly
Before your interview, make sure you have a solid grasp of the Manager, IT, R&D & Regulatory Systems role. Familiarise yourself with Viatris' mission and how this position contributes to their goals in healthcare. This will help you articulate how your skills align with their needs.
✨Showcase Your Technical Expertise
Given the emphasis on Veeva Vault RIM platform experience, be prepared to discuss your hands-on experience with it. Highlight specific projects where you configured, integrated, or migrated systems, and be ready to explain the challenges you faced and how you overcame them.
✨Demonstrate Strong Communication Skills
As the role involves collaboration with various teams, it's crucial to showcase your communication abilities. Prepare examples of how you've effectively translated user requirements into technical specifications and how you've managed stakeholder expectations in previous projects.
✨Prepare for Scenario-Based Questions
Expect questions that assess your problem-solving skills in real-world scenarios. Think about past experiences where you had to manage multiple priorities or navigate complex regulatory environments, and be ready to discuss your approach and the outcomes.