YOUR ROLE
Our central Health, Safety, Environmental and Quality team have an exciting opportunity for a skilled and qualified Healthcare Responsible Person to join their team. This position is ideal for someone eager to advance their career, as we offer comprehensive training and development. You will be responsible for managing two of our Healthcare locations.
WHAT ARE YOU GOING TO DO?
Reporting into the Quality Assurance Manager you will provide technical support and advice to local operational teams focused on quality standards and regulatory guidance. You will manage and conduct training in line with all required ISO standards and healthcare licensing requirements and ensure that the guidelines for GMP and GDP are complied with, and WDA and MIA licenses are maintained. You will safeguard the client and site by ensuring that the quality of medicines, medical devices and other consumer products are not compromised and support and guide site quality managers and controllers in maintaining compliance within their operations.
You engage with operational teams to identify failures and containment issues, by analysing root cause and supporting in remedial actions, acting as a key point of contact for client quality escalations you will collaborate with operational teams to ensure customer complaints are resolved and identify quality improvements, championing a positive change culture. You will conduct bona fide checks, review, and agree quality and technical agreements with clients and suppliers and ensure full compliance with GMDP ensuring contractual and relevant KPIs are monitored, reviewed, and achieved.
WHAT ARE WE LOOKING FOR?
To be successful in your application you will be an experienced and qualified responsible person already operating on a WDA license within a healthcare or third-party logistics environment. You will have detailed knowledge of good distribution practice and good manufacturing practice guidelines, previously working within ISO9001, ISO13485, MDR and IVDR standards and practiced in GDP and GMP requirements for validation, transportation, and packaging.
You will have an inquisitive and logical mindset, skilled at imparting and training best practices across a diverse group of colleagues. It would be desirable, however not essential if you have experience of working within a GMP facility, managing pharmaceutical quality systems or hold a certification as a lead auditor.
WHAT DO WE HAVE TO OFFER?
With a genuine culture of reward and recognition, we want our employees to grow, develop and be part of our journey. We offer a benefits package that includes competitive annual leave entitlement with a fantastic holiday buy scheme, pension and life assurance along with access to an employee benefits platform that offers discounts on gym memberships and money off vouchers for a diverse range of retail, travel and hospitality brands. There’s no doubt that you will be compensated for your hard work and commitment so if you’d like to work for one of the top Logistics providers in the world then please do get in touch to find your next role.
ABOUT TOMORROW
We value your professional and personal growth. That’s why we share plenty of career opportunities for you to thrive within CEVA. Join CEVA for a challenging career.
CEVA Logistics UK&I is committed to attracting, acquiring and retaining the best possible candidates in an equal and inclusive way that is consistent with employment legislation and best practice. We aim to select the best available person for every vacancy irrespective of age, disability, colour, race, nationality, ethnic or national origin, religion or belief, political beliefs, sex, sexual orientation, gender reassignment and marital or civil partnership status.
Please note that candidates will be subject to the necessary right to work checks for the UK and Ireland. IND2
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