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Director R&D Department

Date: Jun 23, 2022

Location: Waterford, IE, D13

Company: Teva Pharmaceuticals

Who Are We?

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 Director R&D to lead the transition of our pMDI portfolio to green propellants based at our site in Waterford

We are searching for talented and motivated individuals that thrive on working in a team oriented, entrepreneurial environment that is dynamic and fast paced. If you are a dedicated, energetic and detail-oriented professional, this could be the perfect role. With your strong scientific credentials, this is a great opportunity to make an impact working with diverse groups across multiple functions in a class leading team. Are you ready for the challenge of working in Teva’s product development group?

A Day in the Life of our Director R&D Department

  • Lead the transition to green propellants for Teva’s global pressurised metered dose inhaler (pMDI) portfolio
  • Lead pMDI products from clinical development through to product registration and beyond
  • Expert level knowledge of global regulatory guidelines for respiratory products
  • Author regulatory submission documents (ANDI, NDA, IND)
  • Lead multidisciplinary teams, comprised of CMC, device engineering, manufacturing operations and any consultants and/or external contractors.
  • Provide enlightened strategic input on the direction of development to senior management and recommend technologies and capital investment.

Who we are looking for

 Are you….

  • Are you educated to PhD Level in (chemistry, pharmaceutical science, chemical engineering, or related field) with extensive experience in a leadership position in the pharmaceutical industry? MBA Would be advantageous.

Do you have….

  • Significant experience leading development of pMDI products from clinical development through to product registration and beyond
  • Demonstrated ability to author regulatory submission documents (ANDI, NDA, IND)
  • Track record of leading multifunctional teams and development projects is essential.
  • Proven project management, planning and influencing skills.
  • Very strong verbal and written communication; collaboration and team building skills; ability to connect with all levels of the organisation.

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

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 sits 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. That’s why we’re constantly looking for ways in which we can learn from each other, embrace what makes us unique and contribute to a fairer society free from discrimination and prejudice