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 are currently seeking a talented and motivated scientist to join our team. In this role, you will take on the responsibility of developing and validating characterization methods for a diverse range of drug products and medical devices. The position provides exciting opportunities for professional growth and skill development in areas such as Extractables & Leachables (E&L), mass spectrometry, and analytical method validation. If you are dedicated, energetic, and detail-oriented, this could be the ideal role for you.

How you’ll spend your day Execution of Extractable and Leachable (E&L) studies, incorporating LC/UV/MS and GC/FID/MS analytical technology Development and validation of analytical methods incorporating Mass Spectrometry detection (LC/UV/MS and GC/FID/MS) Support the characterisation of polymer materials used in medical devices and packaging, including inhalation and injectable drug products, for both small molecules and biopharmaceuticals Assist in the interpretation of Mass Spectrometry (MS) data as part of compound identification studies Compilation and review of detailed technical documents Deliver high levels of customer service (both internal & external) Your experience and qualifications Degree, Masters or PhD qualification in Chemistry (or related discipline), with at least 2 year’s work experience with method development and validation Experience in analytical method development and validation with mass spectrometry is highly desirable Experience with MassHunter software would be advantageous Excellent communicator (both oral and written) Experience of working to current Good Manufacturing Practice (GMP) or Good Laboratory Practice (GLP) and implementing policies and procedures in line with regulatory guidelines Knowledge of global regulatory and compliance requirements Good planning and organising skills & adaptable to changing priorities Contract

A fixed-term contract until the employee's return from maternity leave.

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Teva’s Equal Employment Opportunity Commitment Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.