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 Lead Analytical Scientist at our Waterford site. This is a 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 and the ability to manage and drive projects. If you’re dedicated, energetic and detail-oriented, this could be the perfect role for you!
A Day in the Life of our Lead Analytical Scientist
Lead development and validation of analytical methods for analysis of drug substance/drug product. Lease and coordinate with the formulation team to deliver analytical support for early development/DOE/stability batches. Lead technical investigations and develop approaches to solve wide ranging, interesting and complex problems. Manage outsourced analytical activities at contract facilities and provide technical guidance for method development and pharmaceutical performance testing. Write/review technical documents for regulatory submissions and associated correspondence with regulatory agencies. 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. Taking ownership and responsibility from start to finish of individual projects and tests.
Who we are looking for
Are you….
Educated to Degree or Masters Level (PhD advantageous) in chemistry (or related subject) with strong’ industry experience (5 years plus),
Do you have?
Experience leading the development and validation of analytical methods for UPLC/HPLC and GC is essential. . An understanding of requirements for implementing a QbD approach to method validation and method lifecycle management. Experience delivering technical presentations. Knowledge of global regulatory and compliance requirements. Previous experience of writing/reviewing technical documents. Good planning and organising skills & adaptable to changing priorities. Strong communication and interpersonal skills with previous experience in cross-collaboration 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.