Venn Life Sciences, part of Open Orphan plc, is an Integrated Drug Development Partner offering a unique combination of pre-clinical and CMC drug development expertise, clinical trial design and management. This enables us to create, plan and execute drug and medical device development programs effectively and seamlessly for our clients.
“Our vision” is to play a pivotal role in the development of new products enabling disease prevention and treatment. We do this by creating an environment that generates opportunities for employees to stretch their potential and fully exercise their talents thereby consistently providing outstanding service to our clients. We nurture an environment of respect, pro activity, teamwork and above all keep the patient at the heart of what we do.
We are currently looking for a Clinical QA Manager with hands-on experience to join our team. The successful candidate will have the opportunity to work from one of our European offices and/or home-working with regular visits to our office in Breda.
Reporting to the Head of Quality Assurance, the successful candidate will be responsible for ensuring the robustness and effectiveness of a specific part of the organization’s Quality Management System (QMS) governing the assigned area of regulated operations, across divisions, for Clinical Research. The job also includes the execution of contracted QA services, such as audits on Venn projects or consultancy projects, as assigned.
If you are seeking a rewarding and challenging career this could be the perfect opportunity for you.
How to apply:
Please forward your CV (in English) by email to firstname.lastname@example.org
PLEASE NOTE THAT DUE TO THE HIGH VOLUME OF APPLICATIONS WHICH WE RECEIVE WE WILL ONLY BE ABLE TO REPLY TO CANDIDATES WHOM WE ARE INVITING FOR INTERVIEW.
We do not require the services of agencies for this role.