Essity – a leading global hygiene and health company and the home of brands like Libero, TENA, Libresse, Tork, Sorbact and JOBST is offering an exciting and challenging opportunity for you who want to contribute with your expertise, energy and creativity. We are looking for an additional colleague to join our company as Clinical Evaluation Manager within the Global Marketing and Innovation (GMI) Unit. You
GMI drives company value creation with with global, winning, sustainable innovation and brand building to achieve and sustain category leadership positions. Within GMI we are approximately 750 employees in 12 countries. This role is based in our Mölndal office, in the Global Clinical Affairs department, and report to the Director Clinical Affairs.
Located just a couple of minutes from Mölndal train station in Gothenburg, Essity offers you to be part of an international business setting with over 1000 employees and many contacts across different functions, units and countries. Flexibility is important to us, which is why we believe in a hybrid workplace philosophy. Our office environment is modern with a very special culture focusing on collaboration, innovation, well-being and care, development and commitment. We offer onsite learning, a healthy canteen, social events and many other employee benefits.
Watch our film of why we work at Essity: We are Essity - and we care
About the role
We are looking for a driven and scientifically grounded Clinical Evaluation Manager to join our team. This is a newly established role where you will be instrumental in shaping how we , evaluate, substantiate and communicate clinical evidence for our product portfolio. You will be the subject matter expert in clinical evaluations, ensuring the clinical documentation, including claims, is sufficiently substantiated and aligned with the commercial strategy as well as regulatory requirements, particularly MDR. This role is central to our evidence strategy and plays a key part in product development, life science management incl post-market surveillance, and regulatory compliance.
Examples of tasks
Independently develop and maintain related key documents i.e. Clinical Evaluation Plans and Reports, Literature Search Plans/Reports, State of the Art analyses, and PMCF Plans/Reports.
Perform systematic literature reviews.
Collaborate cross-functionally with stakeholders such as R&D, Regulatory Affairs, Medical Affairs and Commercial .
Provide strategic input on clinical evidence generation and substantiation of claims for new and existing products.
Manage external partners such as Medical Writers and CROs.
Be the Clinical Evaluation subject matter expert in audits and inspections.
Drive the development and refinement of processes and SOPs related to clinical evidence.
Who you are
You are a curious and detail-oriented professional with a strong ability to synthesize complex information. You thrive in a cross-functional environment and are comfortable navigating between scientific rigor and business needs, and you have ability to build relationships and communicate effectively. You have the integrity and confidence to stand by evidence-based conclusions, even when challenged. You enjoy reading, analyzing, and summarizing large volumes of scientific literature and are passionate about ensuring patient safety and product credibility.
You have
Higher academic degree (preferably PhD) in relevant field, e.g. life science or medical. Proven experience in clinical evaluations, ideally within the medical device industry.
Strong knowledge of MDR and related regulatory frameworks .
Experience conducting systematic literature reviews and writing scientific reports.
Excellent communication skills and the ability to collaborate across functions.
High capacity for independent work, critical thinking, and scientific writing.
Fluency in English, both written and spoken.
Application
Interested? If you are up for the challenge and think this sounds like you, apply online today! Kindly note that due to GDPR we will not accept applications via mail.
Please note that since we are in the vacation period, selection of candidates will start from beginning of August.
We may conduct background checks in the final stages of the recruitment process to verify your qualifications and fit for the role
What We Can Offer You
Our purpose, Breaking Barriers to Well-being, provides meaning to everything we do. Working at Essity means a chance to improve well-being for people and opportunities to drive positive change for the society and the environment. As an employee at Essity, you will belong to an organization where you feel valued and supported to grow and challenged to generate business results in a collaborative and open atmosphere. Innovate for Good | Excel Together | Be You with Us
