Who Are We?
We touch the lives of over 200 million patients every day, and billions every year. After all, everyone needs healthcare or medication at some point.
Yet until today, you may not have heard of us.
We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.
We are looking for a Senior Quality Specialist to join our Quality team based in our Baldoyle office. The QA Specialist is responsible for the sale, compliant and efficient execution of job duties in a team environment.
A Day in the Life of a Senior Quality Specialist
You will perform assigned tasks in accordance with procedural requirements and scheduled timelines. Notifying supervisor and other impacted stakeholders if procedural requirements or timelines are not being met.
You will understand cGMPs and procedural requirements for your area of responsibility and be a resource to operators and other personnel to ensure compliance to these requirements.
You will assess and understand events that may not be in accordance with procedures or cGMPs.
You will make decisions consistent with job responsibilities, regulations and procedures and policies whilst providing appropriate comments when needed.
You will perform routine review of documentation generated by personnel to support commercial and development products.
You will author documents that ensure cGMP compliance, such as Standard Operating Procedures, investigations, reports and forms.
Monitor documentation errors and work with personnel to correct documentation, as needed, and develop preventive actions to reduce or eliminate recurrences.
You will draft, review, and approve qualification documentation for production equipment, cleaning validation protocols, Product Quality Reviews SOPs and other documentation.
You will initiate, facilitate, monitor, trend Change Control, Complaints, Deviations, CAPAs and other Quality System documents as required.
You will observe established escalation process for issues impacting established production-related SLAs (Service Level Agreements) and / or fulfilment of production goals.
You will observe all safety and compliance procedures and actively highlight any safety concerns to help drive the reduction of accidents or near misses.
Who We Are Looking For
Are you .
Passionate about delivering results in full whilst sticking to deadlines?
Someone who ensures that their work is right first time?
Do you have .
Prior pharmaceutical or Quality Assurance experience?
Knowledge of cGMP requirements and practices?
Strong analytical skills and knowledge of quality systems such as Trackwise SAP?
Experience using LIMS and Microsoft Office?
Sub Function Quality Assurance Methods Function Quality Already Working TEVA?
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority.
You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply : Internal Career Site
The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR / IT partner.
Teva’s Equal Employment Opportunity Commitment
At Teva, we pride ourselves on being a company where we can all thrive, and where everyone feels comfortable being their true self.
Diversity and inclusion sits at the heart of everything we do. By valuing difference, we can be a better employer for our colleagues, and provide a better service for our customers and patients.
That’s why we’re constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice.