1+ months

Pharmaceutical Technology Specialist I

Salt Lake City, UT 84111
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Company Info

 

Teva is a global pharmaceutical leader and the worlds 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 worlds largest medicine cabinet to 200 million people every day. We offer a uniquely diverse portfolio of products and solutions for patients and we have 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!

 

If youre like people at Teva, you dare to be different. Were making well-being a way of life for our customers and our colleagues. Join us in helping to make healthcare more accessible to more patients, while supporting one of the most innovative teams in the industry.

 

Tevas Salt Lake City, Utah production sites  are two of our complex manufacturing and supply chain operations. We are strengthening and adding to our critical teams with great talent and capabilities. Teva, a global organization, with a brand of evolving success.  Be part of it!

 

We offer a competitive benefits package including Medical, Dental, Vision and Prescription coverage starting on the first day. We also offer Disability and Life Insurance, Paid Time Off, 6% match on the 401(k), Employee Stock Purchase Plan and Tuition Assistance.
 

Job Description

 

Position Summary

 

Under general supervision, the Pharmaceutical Technology Specialist I determines the critical aspects of manufacturing equipment with regard to product and process, and writes protocols and other records related test results.  Prepares final reports that identify the results of protocol testing and the conditions of release.  Assists in conducting efficiency studies and in the identification of process improvement opportunities.  Participates in project coordination activities.


Key Responsibilities 


    Carries out responsibilities in accordance with the organizations policies, procedures, and state, federal and local laws.
    Provides assistance in troubleshooting to manufacturing and packaging areas.
    Interfaces with Quality Assurance and Research & Development (R&D) on process requirements for new and current products.
    Assists with on-site transfer projects and product scale-up activities.
    Recommends improvements in manufacturing and control systems.
    Assures that protocols are approved through proper channels; writes and revises validation protocols.
    Executes validation protocols per related SOPs and assures that acceptance criteria related to validation protocols are met.
    Assures that all test data is gathered and recorded in accordance with cGMP requirements.
    Analyzes data to ascertain if it meets related protocol acceptance criteria; writes deviation reports as required upon failures to meet protocol acceptance criteria.
    Writes reports and assures that they are approved through proper channels.
    Provides support in investigations and other troubleshooting activities.
    Prepares batch record documentation.
    Develops and communicates project timelines and status.
    Complies with all GMP and safety requirements, SOPs and Company policies and procedures.
    Performs related duties as assigned. 
 

Qualifications

 

Education/Experience

 

  • Bachelors degree in Science or related field from an accredited college or university and one (1) experience; or an equivalent combination of education and experience.  
  • Requires a minimum one (1) year of process technician or laboratory experience in a manufacturing environment.
  • Knowledge of or ability to learn pharmaceutical manufacturing principles, practices and applications 
     
Function
Manufacturing
Sub Function
Technical Transfer
Reports To

Senior Principal Pharmaceutical Technology Specialist 

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.

Posted: 2020-08-26 Expires: 2020-10-24

Join us at the forefront of pharmaceutical research and production. With state-of-the-art facilities, highly skilled colleagues, and a high-powered organizational culture, Teva offers you countless possibilities to make a real difference in people's lives and add value to your career.

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Pharmaceutical Technology Specialist I

Teva Pharmaceuticals
Salt Lake City, UT 84111

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