At a Glance
- Tasks: Lead life cycle management and submissions for innovative healthcare products.
- Company: Join a leading healthcare organisation with a focus on innovation.
- Benefits: Flexible working options and opportunities for career growth.
- Other info: Collaborate with cross-functional teams in a fast-paced environment.
- Why this job: Make a real impact in regulatory affairs while managing a dynamic team.
- Qualifications: Experience in EMEA Regulatory Affairs and strong knowledge of EU procedures.
The predicted salary is between 70 - 70 Β£ per hour.
Your new company Are you an experienced Regulatory Affairs professional looking to take ownership of life cycle strategy across a dynamic EU portfolio? We're partnering with a leading healthcare organisation to find a Regulatory Affairs Consultant, life cycle management, to join their growing team. This is a fantastic opportunity to play a key strategic and operational role across product life cycle management, working at the intersection of CMC, regulatory strategy, and cross-functional collaboration. You'll contribute to both innovation and maintenance of existing products while managing a small team.
Your new role Key Responsibilities Life cycle Management & Submissions Lead end-to-end life cycle management activities including variations, renewals, labelling updates, and aggregate reports. Prepare and submit variation applications via EU procedures (MRP/DCP, Workshare), including complex submissions and super-groupings. Develop submission strategies, including reference member state selection and regulatory pathways Support marketing authorisation applications for early-stage innovation projects Regulatory Strategy Provide strategic regulatory input and technical CMC guidance to cross-functional stakeholders Partner with product development teams to define regulatory requirements, risks, and timelines Contribute to the design and execution of development programmes across the EMEA region Compliance & Governance Ensure compliance with EU and global regulatory requirements and maintain inspection readiness Stay up-to-date with evolving regulatory frameworks, advising the business on impact and opportunity Oversee and maintain accuracy of regulatory systems and documentation Support audits and ensure SOP adherence and continuous process improvement.
What you'll need to succeed Proven experience in EMEA Regulatory Affairs, ideally within lifecycle management Strong knowledge of EU regulatory procedures (MRP/DCP, variations, PSUSA/aggregate reports) Demonstrated ability to develop and execute regulatory strategy across complex submissions Must have strong working knowledge of worksharing and super grouping Experience in line management or mentoring junior team members Excellent stakeholder engagement and cross-functional collaboration skills.
What you'll get in return Flexible working options available.
What you need to do now If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you, but you are looking for a new position, please contact us for a confidential discussion about your career.
Regulatory affairs Manager post approval MRP DCP in Reading employer: Hays Life Sciences
Join a leading healthcare organisation that values innovation and collaboration, offering a dynamic work environment where you can take ownership of life cycle strategy across a diverse EU portfolio. With flexible working options and a strong focus on employee growth, this company fosters a culture of continuous improvement and support, making it an excellent employer for those looking to make a meaningful impact in regulatory affairs.