Product Owner Global Regulatory Affairs (m/f/d)
Join to apply for the Product Owner Global Regulatory Affairs (m/f/d) role at Grünenthal Group
Product Owner Global Regulatory Affairs (m/f/d)
Join to apply for the Product Owner Global Regulatory Affairs (m/f/d) role at Grünenthal Group
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Our Corporate Functions teams make sure everything at Grünenthal runs smoothly by bringing together people with a wide range of skills – from experts in finance, IT, HR, law and compliance through to business strategists and creative media minds. If you’re a great collaborator and a strong communicator, you’ll feel right at home here. Join our team and join forces with colleagues across our business to maximise our company’s positive impact on patients and their families.
What The Job Looks Like
Each day you'll enjoy a variety of challenges, such as:
* Co-create the Development data and IT solution landscape and roadmap for GRA
* Partner with internal and external stakeholders and driving innovation
* Ensure that all IT products are compliant with internal security, risk management policies and practices, external regulatory and statutory requirements
* Orchestrate our stage gate/demand process to bring ideas to new IT solutions, helping Development to identify and promote the most beneficial ideas
* Guide a product-oriented IT team that owns E2E all GRA IT solutions
* Act as program manager and ensure excellence in project set-up and execution
* Ensure E2E availability and quality of GRA Solution Services
* Communication/reporting of R&D IT projects / Solution Services to all relevant stakeholder for the domain
What You'll Bring To The Table
To make the most of this role and truly thrive, you should have:
* Minimum 8 years of experience, working in life science technology environment, preference in scientific technology
* Masters’ degree or equivalent experience in science, engineering, computing, bioinformatic, or similar
* Experience in IT strategy development, solution design, project delivery and service management
* Good understanding & experience with RIM Functional Processes – Registrations Management, Submission Planning, Submission Content Planning, Document Management, Publishing etc.
* Good understanding of Regulatory business process & requirements (Marketing Authorization, Renewals, Variations, Labeling, etc.) – EU & US
* Fluent in business English, German is a plus
* Proven skills in project/product mgmt. teamwork, leadership
* Excellent analytical, organizational, communication and presentation skills at senior level for working with cross-functional teams and stakeholders, strategic thinker and outstanding collaborator
* A customer-centric mindset and a passion for innovation and problem-solving
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Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Legal, Business Development, and Information Technology
* Industries
Pharmaceutical Manufacturing, Hospitals and Health Care, and Biotechnology Research
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