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Analytical Researcher Product Development Respiratory R&D

Date: Mar 11, 2019

Location: Waterford, IE, X19

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

Role outline: The role is of critical importance 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 analytical pharmaceutical product development. If you’re dedicated, energetic and detail-oriented, this could be the perfect role for you.


The ideal individual will have specialised skills and experience gained from working at the forefront of respiratory product development (or a related area). They will have experience in multivariate data analysis plus a strong appreciation of the technical and regulatory challenges associated with developing robust products for global markets.

Responsibilities

  • Lead scientific/technical investigations and independently develop approaches to solve wide ranging, difficult and complex problems.
  • Lead product development teams and/or processes, characterization, investigations and root cause analyses.
  • Represent respiratory analytical sciences at international global fora.
  • Specialist in compilation and review of detailed technical documents.
  • 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 such as Manufacturing, QC, QA, Regulatory Affairs and Operations to address deficiencies, fillings of new regulatory applications etc.
  • Effective and timely written and verbal communication.
  • Contribute to production of Module 3 regulatory submissions and associated correspondence with regulatory agencies.
  • Deliver customer service (both internal & external) through project timelines in accordance with company procedures & regulatory guidelines.

Qualifications

Education / Experience

  • Preferably a Doctorate or Masters qualification in chemistry (or related subject) with demonstrable industry experience preferably in respiratory product development.
  • Strong Multivariate Data Analysis skills.
  • Proven project management, planning and influencing skills.
  • Knowledge of global regulatory and compliance requirements.
  • Experience of working to current Good Manufacturing Practice and/or 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.

Function

Research & Development

Sub Function

Drug Development and Preclinical Studies

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, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws.

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