Analytical Researcher
Date: Sep 19, 2024
Location: Waterford, Ireland, X91
Company: Teva Pharmaceuticals
Job Id: 58419
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 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 Researcher
* Lead/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 development.
* Write/review 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) to address deficiencies and filings of new regulatory applications.
Who we are looking for
Are you…
* Educated 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 a pharma environment.
* Knowledge of global regulatory and compliance requirements.
* Experience in writing/reviewing technical documents.
* Good planning and organizing skills & adaptable to changing priorities.
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 sit 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.
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