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Grünenthal Group

Grünenthal Group

www.grunenthal.com

2 Jobs

4,600 Employees

About the Company

Grunenthal is a global leader in pain management and related diseases. As a science-based, fully-integrated pharmaceutical company, we have a long track record of bringing innovative treatments and state-of-the-art technologies to patients worldwide. Our purpose is to change lives for the better - and innovation is our passion. We are focusing all of our activities and efforts on working towards our vision of a world free of pain. Grunenthal is headquartered in Aachen, Germany, and has affiliates in 28 countries across Europe, Latin America and the US. Our products are available in approx. 100 countries. In 2024, Grunenthal employed around 4,300 people and achieved revenues of EUR 1.8 bn. More Information on www.grunenthal.com Jobs & Career: http://careers.grunenthal.com/ Imprint: https://www.grunenthal.com/en/footer-links/imprint Privacy: https://www.grunenthal.com/en/footer-links/privacy-statement-social-media This company profile is managed by Global Communications. In our commitment to transparency and the principles outlined in our digital ethics charter, Grunenthal wishes to inform you that generative artificial intelligence technologies are occasionally used to enhance content on this channel. Each content piece has been reviewed and edited by a team member before publication to ensure accuracy.

Listed Jobs

Company background Company brand
Company Name
Grünenthal Group
Job Title
Product Owner Global Regulatory Affairs (m/f/d)
Job Description
**Job Title** Product Owner Global Regulatory Affairs (m/f/d) **Role Summary** Owns and drives the development, delivery, and ongoing optimization of IT solutions that support Global Regulatory Affairs (GRA). Acts as bridge between regulatory, development, IT, and other cross‑functional stakeholders to ensure regulatory processes are fully digitalized, compliant, and efficient. **Expectations** - Minimum 8 years of life‑science or scientific technology experience. - Master’s degree (or equivalent) in science, engineering, computing, bioinformatics, or related field. - Proven expertise in IT strategy, solution design, project delivery, and service management. - Strong grasp of regulatory processes (EU/US marketing authorization, renewals, variations, labeling, etc.) and RIM functional processes (registrations, submission planning/content, document management, publishing). - Fluency in business English; German is an advantage. - Senior‑level communication, analytical, and leadership skills; customer‑centric mindset. **Key Responsibilities** - Co‑create and maintain the GRA IT solution landscape and roadmap. - Partner with internal and external stakeholders to identify, prioritize, and innovate new IT solutions. - Ensure all IT products comply with internal security, risk management policies, and external regulatory/statutory requirements. - Orchestrate stage‑gate/demand processes, guiding the product‑oriented IT team through end‑to‑end ownership of GRA solutions. - Act as program manager: set up projects, manage execution, and maintain quality and availability of GRA solution services. - Communicate progress, risks, and outcomes of R&D IT projects to all relevant stakeholders. - Champion continuous improvement and customer‑centric innovation across the regulatory IT domain. **Required Skills** - IT strategy & architecture development - Product and project management (Agile/Scrum preferred) - Regulatory affairs knowledge (EU/US) - RIM process expertise (registration, submission planning/content, document management, publishing) - Risk management & compliance oversight - Cross‑functional leadership & stakeholder engagement - Analytical problem solving and decision making - Excellent written and verbal communication, presentation at senior level - Customer‑centric mindset and passion for innovation **Required Education & Certifications** - Master’s degree (or equivalent) in science, engineering, computing, bioinformatics, or related discipline. - Professional certifications in product/project management (e.g., PMP, PRINCE2, CSPO) are a plus.
Brussels, Belgium
On site
Senior
16-10-2025
Company background Company brand
Company Name
Grünenthal Group
Job Title
Global Medical Lead Early Assets
Job Description
**Job Title:** Global Medical Lead Early Assets **Role Summary:** Lead and coordinate medical strategy, patient engagement, and evidence generation for early‑stage therapeutics in Duchenne Muscular Dystrophy (DMD) and related rare diseases. Collaborate across R&D, Commercial, and Medical Affairs to define product hypotheses, alignment with stakeholder needs, and integrated evidence plans that support regulatory, payor, and clinical uptake. **Expectations:** - Build and maintain networks with Key External Experts (KEEs), Patient Advocacy Groups (PAGs), and scientific societies. - Translate patient and KEE insights into actionable product development and positioning. - Provide expert medical oversight, scientific storytelling, and evidence generation strategies aligned with commercial objectives. - Ensure compliance with regulatory, legal, and ethical standards. **Key Responsibilities:** - Establish and manage patient organization and scientific society networks for DMD. - Develop and execute engagement plans for PAGs and KEEs; organize advisory boards. - Collaborate with early‑product leads to define Target Product Profiles (TPPs) and product hypotheses. - Partner with R&D diligence teams to clarify value propositions and positioning. - Lead scientific discussions, study program design, and lifecycle management initiatives. - Create scientific/medical narratives and messaging consistent with patient journey and unmet needs. - Monitor competitive landscape and deliver updates and training. - Align evidence generation plans with regulatory submission, clinical practice, and commercial launch. - Identify and fill evidence gaps for regulators, payers, prescribers, and patients. - Outline clinical trials, real‑world studies, HEOR, biomarker research, and integrate insights across functions. **Required Skills:** - Deep knowledge of clinical practice, guidelines, and standards in rare diseases, especially DMD. - Experience engaging PAGs and KEEs, with DMD-specific experience a plus. - Strong medical and scientific acumen; ability to translate complex data into clear narratives. - Expertise in early product evaluation and drug development lifecycle. - Knowledge of regulatory, compliance, legal, and evidence generation requirements. - Excellent stakeholder relationship building, communication, and collaboration. - Familiarity with biological pathways of DMD and existing therapeutic options preferred. - Ability to develop Integrated Evidence Plans and coordinate with U.S. regulatory priorities. **Required Education & Certifications:** - MD, PhD, PharmD, or related advanced degree in a life‑sciences discipline. - Relevant professional certifications in medical affairs, clinical research, or regulatory affairs (e.g., CMHA, RRT) preferred.
Brussels, Belgium
On site
Senior
16-10-2025