Senior Manager R&D Quality

Who we are

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. 
We're Teva, a global pharmaceutical company, committed to increasing access to high-quality healthcare to patients around the world.

We would like to invite applications for the role of Senior Manager R&D Quality located at our Waterford site.

The Senior Manager R&D Quality role is part of a team providing Quality Assurance (QA) leadership to the day to day activities of the Research and Development (R&D) and Teva Digital Health (DH) units. This role is involved in working with a dynamic and fast moving R&D Environment and offers the chance to gain a wide range of experience. There is the option for people management as part of this role. This role is desirable for someone who is already a QP or is interested in gaining that qualification. 

A Day in the Life of our Senior Manager R&D Quality

• Reporting on the performance of the quality system, reviewing and approving batch documentation, investigation reports, change requests, SOP’s, qualification reports and ensuring they are completed right first time and in full in accordance with Good Manufacturing Practice requirements
• To develop, maintain, implement and improve quality standards and systems which give assurance that products comply with clinical dossiers, specifications and cGMP’s. To take ownership where needed
• Responsible to support clinical trial batch release / new product submissions / launch.  
• Carrying out audits to ensure that all operational processes are in compliance with the required standards conforming to Company GMP, GLP, SOP’s, Specifications, Clinical/Submission dossier/ Technical Documentation requirements. Auditing of vendors/suppliers/CMO’s as required.
• Ensuring that the quality system requirements are effectively established and efficiently maintained in accordance with the regulations.

Who we are looking for

Are you…. 

• Educated to Degree or Masters Level in a science related subject.

Do you have?

• Extensive experience in Quality Assurance/Quality Auditing at senior level. 
• Extensive R&D experience in an FDA / HPRA approved facility.
• Expertise in regulatory requirements with respect to at least one of Pharmaceutical / Medical Devices / Combination Products
• Qualified Person status/eligibility is preferable.
• Knowledge of cGMP, GLP, Regulatory Bodies and Customer requirements
• Decision making experience 
• Planning & Organising Skills

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