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Global IT Manager

Date: May 7, 2019

Location: Waterford, IE, WA7 3FA

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 are currently searching for a Global IT Manager to join our Global IT Team, based at our office in Waterford.  As Global IT Manager you will be responsible to provide scope validation strategies for global systems such as ELN, SDMS, Fusion, etc.  Key individual will align closely with R&D and help determine effective and efficient mechanisms to build compliance and quality into the technical solutions.  The role will work closely with QA IT, R&D, and internal team to reduce lengthy validation processes and optimize them for quick delivery.  In addition to validation and technical aspects, the individual will step in as project management duties for projects related to system enhancements, site implementations, and new technology adoption.


Key Responsibilities: 

 

  • Provide production support to Global R&D sites for ELN and SDMS
  • Validation, Technical, and PM support for current and new workflow enhancements
  • Interface directly with various Business, QA and IT functional areas.
  • Provide compliance and quality guidance to project team during and post implementation regarding CSV requirements.
  • Provide guidance on system design and technical configurations where capable
  • Provide guidance to Test Script Writer/Tester
  • Provide guidance to project teams regarding the development of validation strategies
  • Review and contribute to SOP revisions
  • Execute Periodic Reviews of Computer Systems

Qualifications

  • Bachelor’s Degree preferably in Computer Science, Information Systems Management, Computer Engineering, Electrical Engineering, or a related field, degree in life sciences, or equivalent combination of relevant education and experience.
  • Proven experience working in a highly regulated environment within the Pharmaceutical Industry.
  • Extensive knowledge and experience of cGMP and its implementation to laboratory instrumentation and laboratory processes.
  • Experience in writing validation documents is essential.
  • Experience in 21 CFR Part 11, GAMP
  • Experience in SDLC (Agile or Waterfall)
  • Successful experience working in a team environment and with a multi-disciplinary and global team.
  • Strong compliance and quality mind, with ability to mirror technical knowledge, and science.
  • Excellent customer service skills.
  • Excellent Organizational Skills.
  • Strong problem-solving skills.
  • Willingness to travel.

Function

Information Technology

Sub Function

IT Business Application

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.