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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 Analytical Researcher at our Waterford Site-Perm position.
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 strength 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 ResearcherLead/perform analytical method development and validation for drug substance/drug product (HPLC/UPLC, GC, KF, UV, FT-IR ). Liaise and coordinate with the formulation team to deliver analytical support for early development/DOE/stability batches. Participate in technical investigations and develop approaches to problem solving challenges which arise in early developmentWrite/reviewing technical documents for regulatory submissions and associated correspondence with regulatory agencies.Work with third party contract lab facilities to develop and transfer analytical methods.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' e.g Operations, QC, QA, Regulatory Affairs and Operations to address deficiencies, fillings of new regulatory applications etc.
Who we are looking forEducated to degree or Masters Level in Chemistry, (or related subject) with Strong industry experience preferably in an R&D environment.Do you have… Experience of development and validation of analytical methods for UPLC / HPLC / GC/Raw materials. Ideally 1-2 years of experience in pharma environmentKnowledge of global regulatory and compliance requirements.Writing/reviewing technical documents.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 CommitmentAt 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.
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