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Analyst - R&D

Date: May 15, 2019

Location: Waterford, IE, X91

Company: Teva Pharmaceuticals

Company Info

Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to improving health and increasing access to quality health solutions worldwide. Our employees are at the core of our success, with colleagues in over 80 countries delivering the world's largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we've built a promising pipeline centered around our core therapeutic areas.  We are continually developing patient-centric solutions and significantly growing both our generic and specialty medicines business through investment in research and development, marketing, business development and innovation. This is how we improve health and enable people to live better, healthier lives. Join us on our journey of growth!

Job Description

We would like to invite applications for the role of R&D Analyst Product Development Respiratory R&D

The role is important to maintain Teva’s strength in combination product development and to help deliver on the Respiratory long range plan. Respiratory R&D is seeking a highly innovative, data-driven and self-motivated individual with strength in the analysis & characterisation of respiratory products or with other product platforms. If you’re dedicated, energetic and detail-oriented, this could be the perfect role for you!

Key responsibilities

  • Provide analytical support to the R&D team on time and in full to meet the objectives of the department
  • Perform inhalation testing to support stability, characterisation, product development etc. for (HFA and Dry Powder) using existing and innovative technologies and automated equipment
  • Reporting / Reviewing test details and results using electronic laboratory notebooks and / or spreadsheets as required.
  • Validation of analytical & test methods for raw materials and respiratory finished products.
  • Transfer methods to and from other TEVA Global groups and contract facilities
  • Identify and make recommendations for improvements as part of a team within or outside department in order to eliminate non value added activities and ensure continuous improvement
  • Compilation and review of technical protocols and reports
  • Contribute to and support the R&D team in delivery a high standard of service to both internal and external customers
  • Provide guidance, support and training in areas of expertise and knowledge to other analysts to ensure they are equipped to carry out tasks assigned to them
  • Ensure that all work is carried out in compliance with the required standards conforming to company, cGMP, GLP, SOP, specifications, validation, regulatory affairs, H&S and environmental requirements


  • 3rd Level degree in Chemistry or Pharmaceutical Science related discipline with proven laboratory experience.
  • Experience in HPLC/UPLC analysis including troubleshooting is essential.
  • Knowledge of global regulatory and compliance requirements.
  • Experience of working to current Good Laboratory Practice and implementing policies and procedures in line with regulatory guidelines.
  • Strong verbal and written communication; collaboration and team building skills.
  • Excellent planning and organising skills & adaptable to changing priorities.
  • Ability to take responsibility and work on one’s own initiative.


Research & Development

Sub Function

Drug Analysis and Formulation

Reports To

In process of validation

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.

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