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. 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 would like to invite applications for the role of Analytical Researcher R&D at our Waterford Site-Perm role.

The role is an exciting opportunity to work within the dynamic and ever-changing environment of R&D as part of the product development team for a global leader in the pharmaceutical sector. Teva Respiratory R&D is seeking a highly innovative, data-driven and self-motivated individual with proven ability in analytical pharmaceutical product development. If you’re dedicated, energetic and detail-oriented, this could be the perfect role for you.

 

A day in the life of our Analytical Researcher R&D

 

 

Lead/involved in scientific/technical investigations and develop approaches to solve wide ranging, difficult and complex problems. Lead/involved in product development teams and/or processes, characterization, investigations and root cause analyses. Compilation and review of detailed technical documents. Ensure that all work is carried out in compliance with the required standards conforming to company, cGMP, GLP, SOP, regulatory, H&S and environmental requirements. Work with cross-functional departments such as Manufacturing, QC, QA, Regulatory Affairs and Operations to address deficiencies, fillings of new regulatory applications etc. Effective and timely communication-both written and verbal Contribute to production of Module 3 regulatory submissions and associated correspondence with regulatory agencies. Deliver customer service (both internal & external) through project timelines in accordance with company procedures & regulatory guidelines.
  Who we are looking for

 

 

Are you…. 
 

Educated to BSc degree level in a Science Discipline (Chemistry background preferred) with proven industry experience

 
Do you have…
 

Experience working to current Good Manufacturing Practice and/or Good Laboratory Practice and implementing policies and procedures in line with regulatory guidelines. Multivariate Data Analysis skills. Experience with analytical method validation  Chromatography experience using analytical methods (HPLC/UPLC) Knowledge of global regulatory and compliance requirements. Strong verbal and written communication; collaboration and team building skills. Good planning and organising skills & adaptable to changing priorities. 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