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Analytical Researcher
Date: Sep 4, 2025
Location:Waterford, Ireland, X91
Company: Teva Pharmaceuticals
Job Id: 63744

WHO WE ARE

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

THE OPPORTUNITY

We would like to invite applications for the role of an permanent Analytical Researcher position at our Waterford Site.
This provides 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!

Key Responsibilities:

• Heavily involved, or occasion leading, scientific/technical investigations and develop approaches to solve wide ranging, difficult and complex problems.
• Working closely with product development teams and/or processes, characterisation, investigations and root cause analyses.
• Compilation and review of detailed technical documents.
• Ensuring that work is carried out in compliance with the required standards conforming to company, cGMP, GLP, SOP, regulatory, H&S and environmental requirements.
• Working cross-functionally with significant communication channels between departments such as Manufacturing, QC, QA, Regulatory Affairs and Operations to address deficiencies, fillings of new regulatory applications etc.
• Contributing to production of Module 3 regulatory submissions and associated correspondence with regulatory agencies.
• Delivering excellent customer service (both internal & external) through project timelines in accordance with company procedures & regulatory guidelines.

YOUR EXPERIENCE AND QUALIFICATIONS

Do You Have:

• Career experience within a Pharmaceutical laboratory setting.
• Experience working to current Good Manufacturing Practice and/or Good Laboratory Practice and implementing policies and procedures in line with regulatory guidelines.
• Knowledge of global regulatory and compliance requirements.
• Excellent planning and organising skills & adaptable to changing priorities.

Are You:

• Bringing a breadth of data analysis skills.
• A confident communicator both verbally and in writing.
• Valuing colleague collaboration and team building.

If so, we’d value hearing from you!

• Heavily involved, or occasion leading, scientific/technical investigations and develop approaches to solve wide ranging, difficult and complex problems.
• Working closely with product development teams and/or processes, characterisation, investigations and root cause analyses.
• Compilation and review of detailed technical documents.
• Ensuring that work is carried out in compliance with the required standards conforming to company, cGMP, GLP, SOP, regulatory, H&S and environmental requirements.
• Working cross-functionally with significant communication channels between departments such as Manufacturing, QC, QA, Regulatory Affairs and Operations to address deficiencies, fillings of new regulatory applications etc.
• Contributing to production of Module 3 regulatory submissions and associated correspondence with regulatory agencies.
• Delivering excellent customer service (both internal & external) through project timelines in accordance with company procedures & regulatory guidelines