Walker James Group are currently representing a global biopharmaceutical company as they seek to add an experienced Qualified Person to their team.
Our client is a leader in their field, with an incredibly well established and respected product portfolio that has provided a platform for continued and sustained growth. With further treatments in development, they have an impressive outlook for 2025 and beyond which is also the driver behind significant investment at this particular site, as they seek to expand their capability and production output, which in-turn will be hugely impactful for their patients.
As a Qualified Person (QP) you will take a leading role across quality actions for the site, supporting in the regulatory compliance and QP certification of batch releases in accordance with UK and EU requirements. Furthermore you will:
* Be well versed in Quality Assurance, working closely alongside product development teams to stringently manage the introduction and disposition of clinical materials.
* Offer leadership and mentoring throughout, your actions will foster a culture of 'Commitment to Quality' which will be underpinned by the necessary framework instilled across the Quality function.
* Assist throughout regular audits for varying governance.
* Be eligible to act as a QP within the pharmaceutical industry as well as having proven experience operating at a technically high level within a sterile manufacturing environment.
On offer is a competitive salary which is complemented by an extensive benefits package, incl. annual bonus, generous pension and wellness allowance amongst others.
You will be joining this business at a really exciting time in their journey. This site alone has seen repeated recognition in the 'Best Workplaces' awards, attributed to a diverse and inclusive culture whilst creating an environment where employees feel valued and empowered to be impactful in their work.
Please note this is a hybrid role where the expectation will be for a minimum of 3 days per week on site.