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The Company
Eisai is a leading research based pharmaceutical organisation with an extensive portfolio across the Oncology, Neurology and Pain therapy areas.
By joining Eisai, you will be working for an organisation with a human healthcare philosophy, which means that we put the patient first in everything we do.
Your new role
As the Qualified Person (QP), you will be responsible for supporting the Associate Director Quality Operations in the implementation and maintenance of EML’s Quality Assurance activities relating to product support used for the manufacture, packaging, testing, storage and distribution of marketed products. Ensuring that operations are compliant with current GMP and Eisai Corporate expectations. Enhancing quality policies, systems and procedures as appropriate.
Carry out legal duties of a Qualified Person (QP) as specified under EC directive 2001/83/EC as amended and 2001/20/EC.
What are we looking for?
What we offer in return
Eisai offers a competitive salary and excellent wider benefits package that includes,
What you need to do next
If you are interested in this position, please click ‘apply now’ at the top of this advert. Upon submitting your application, you will be asked to complete your profile and upload a copy of your CV along with any additional information to support your application.
If you have any questions, please contact us on [email protected]
Eisai Recruitment Statement
Diverse perspectives and experiences are critical to our success, and we welcome applications from all people from all backgrounds with the experience and skills needed to perform this role. We look forward to receiving your application.
Eisai EMEA EDI Commitment Statement
We believe that diverse and inclusive teams promote wellbeing, learning and innovation, helping Eisai serve our patients, their families, our employees, and
society.
Our commitment is: