We are DEBRA. We were established in 1978 by Phyllis Hilton, whose daughter Debra had epidermolysis bullosa (EB), as the world’s first EB patient support organisation. Today we are national charity that supports over 4k members, which includes people living with all forms of EB, their families, and carers, plus healthcare professionals and researchers who work with EB. We are also one of the world’s largest investors into EB research. We employ over 300 colleagues and can count on the support of over 1200 volunteers who support us across our network of charity shops located throughout England and Scotland. Will you join us on our journey to a world where no one suffers with EB?
is a world where no one suffers with epidermolysis bullosa
is that we live in a world where no one suffers with epidermolysis bullosa (EB) and we provide life-long care, while seeking cures, for all those affected/impacted by living with EB.
Our values are based around care, inclusivity, and making a difference. These values are the foundation of our culture are help make DEBRA a great place to work
We offer a competitive salary, along with rewards & benefits which include
Auto Enrolment Pension with DEBRA contribution
Life Assurance Scheme
Employee Assistance Program
Personalised Recognition Awards
Opportunities for Apprenticeships and Internships
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“The issues for those living with EB are compelling and emotive and this is what has drawn us all towards supporting such a worthwhile cause. I feel that my life has been enriched by the experiences I have had since becoming Patron of DEBRA, mainly through the patients I have met at a variety of functions. I never knew how much the human body could withstand in terms of suffering until I understood more about how people with EB live with their condition”
“I feel very relevant to DEBRA, having spent so much time having dressings changed, having healing skin pulled off because that’s what dressings do, having itch beyond all comprehension. I understand something of the pain and suffering that people with EB endure every day. I want to do what I can to fight EB and raise the profile of the condition.”
“It is such a supportive place to work, no matter what function you are in, everyone pitches in to help you be your best. It gives me a great sense of pride to know that I am helping, in my small way, to deliver something amazing to the sufferers of EB, and their families.”
“With over 15 years’ experience at DEBRA, I enjoy working with the teams at DEBRA, alongside working with the management or the excellent volunteers, every day is challenging but extremely rewarding. It is a privilege to meet people with EB, reminding me why I am passionate, and take pride in my work.”
“Since I started working for DEBRA, I have gained so much knowledge on EB and this is why I love coming to work every day to helps the EB community and find a cure for this horrible disease”
“I enjoy and look forward to going to work because of my amazing team”