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Chemist I

Date:  Mar 3, 2023
Location: 

Salt Lake City, Utah, United States, 84116

Company:  Teva Pharmaceuticals
Job Id:  44048

Who are we?

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

Under general supervision, performs cGMP laboratory analyses of Finished products and in process materials. Performs stability testing for Finished products. Performs maintenance and calibration of analytical instruments.

 

Essential functions include:

  • Carries out responsibilities in accordance with the organization’s policies, procedures and state, federal and local laws.    
  • Operates general analytical instruments during the testing of finished products using HPLC, UPLC, GC-FID, UV-VIS, FTIR, automatic titrators, Dissolution Apparatus, particle size analyzer, Instron, Densitometer, Rheometer, viscometer (LV/RV/Cone and Plate), pH meter and analytical balance.
  • Prepares standard, sample, and buffer solutions as required by test methods and performs all necessary calculations associated.
  • Labels, transcribes and records documentation such as report sheets and laboratory notebooks as required by SOPs.
  • Cleans, maintains and calibrates laboratory equipment to ensure compliance with current Good Manufacturing Procedures (cGMP).
  • Meets project deadlines and performance standards as assigned.
  • Complies with all Company policies and procedures, including safety rules and regulations     
  • Performs related duties as assigned.

Qualifications

Bachelor’s Degree in Science or related science field from an accredited college or university or one (1) year related laboratory experience or an equivalent combination of education and experience.


Experience and Skills:

 

  • Usage of GC and HPLC chromatographic equipment, as well as UV/VIS, dissolution apparatuses, FTIR, Instron operation and other techniques in testing gels, creams, lotions, oral solutions and transdermal system.
  • Business, scientific and personal computer hardware and software applications.
  • Business English usage, spelling, grammar and punctuation.
  • Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures.
  • Knowledge of or ability to learn FDA, cGLP, cGMP, USP, EP and SOP or other applicable regulatory and safety compliance guidelines.
  • Performing testing accurately and precisely.
  • Responding to routine inquiries from management, employees and regulatory agencies.
  • Communicating clearly and concisely, both orally and in writing.
  • Managing multiple projects, duties and assignments.
  • Establishing and maintaining cooperative working relationships with others.

Function

Quality

Sub Function

Manufacturing Quality Control

Reports To

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

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.  We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

 

Teva Pharmaceuticals USA requires all U.S. new hires to be fully vaccinated for COVID-19 prior to the first date of employment. As required by applicable law, however, Teva will consider requests for reasonable accommodations.

ection under applicable laws.