Senior Regulatory Affairs Manager
Essity Aktiebolag (publ) / Biomedicinjobb / Mölndal
2026-06-17
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hela Sverige This is a senior, global regulatory leadership role within Central Function Digital Transformation and Business Enablement (DT&BE) , working with Personal Care, with a strong focus on medical devices in continence care. Based in Gothenburg, you will lead a team of regulatory managers and specialists while acting as the key regulatory business partner for the category.
You will operate across the full product lifecycle — from early innovation and regulatory strategy to market maintenance — ensuring compliance with European and US medical device regulations. Working in a complex matrix organization, you will collaborate closely with R&D, Quality, Marketing, and regional regulatory teams to enable compliant, efficient, and business‐focused decision‐making.
The position is located in Gothenburg and reports to the Global Regulatory Affairs Director.
What You Will Do
• Regulatory Leadership: Lead, coach, and develop a team of regulatory managers and specialists in a global, matrix organization
• Regulatory Strategy: Define and drive regulatory strategies for medical device products from early development through lifecycle management
• Business Partnership: Act as the regulatory business partner for the category, advising stakeholders on regulatory impact, risks, and opportunities
• Project Support: Provide regulatory guidance in innovation and change projects, ensuring compliant and timely execution
• Compliance Management: Ensure products, technical documentation, and labeling remain compliant with evolving global regulations
• Stakeholder Collaboration: Coordinate with regional regulatory teams and external stakeholders to enable successful market access
• Process Improvement: Drive harmonization of regulatory ways of working and contribute to continuous improvement initiatives
Who You Are
You are a seasoned regulatory affairs professional with leadership capabilities and a strategic mindset. You bring deep expertise in medical device regulations, thrive in complex global environments, and are able to balance compliance requirements with business needs. With a collaborative and pragmatic approach, you confidently guide teams and stakeholders through regulatory challenges while driving high-quality, timely outcomes.
You have:
• A university degree in a scientific or technical discipline relevant to regulatory affairs
• Solid experience in regulatory affairs for medical devices, with strong knowledge of European and US regulations
• Proven ability to work effectively in global, matrix‐driven organizations and manage complex regulatory topics
• A confident communicator with strong project management skills, able to perform under pressure and navigate audits, complaints, and tight timelines
• Full professional proficiency in English
Så ansöker du Sista dag att ansöka är 2026-06-28
E-post:
magnus.blixt@essity.com Omfattning Detta är ett heltidsjobb.
Arbetsgivare Essity Aktiebolag (publ) (org.nr 556325-5511)
Mölndals bro 2 (
visa karta)
431 31 MÖLNDAL
Arbetsplats Essity Hygiene and Health AB (Mölndal)
Jobbnummer 9968825