Chemist at Teva Pharmaceuticals
Salt Lake City, UT 84108, USA -
Full Time


Start Date

Immediate

Expiry Date

15 Oct, 25

Salary

0.0

Posted On

15 Jul, 25

Experience

1 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Lotions, Software, Grammar, Writing, Spelling, Regulatory Agencies, Chemistry, Ep, Wet Chemistry, Ftir, Punctuation, Cglp, Documentation

Industry

Pharmaceuticals

Description

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Chemist
Date: Jun 30, 2025
Location:Salt Lake City, United States, Utah, 84108
Company: Teva Pharmaceuticals
Job Id: 62598

WHO WE ARE

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

EDUCATION/CERTIFICATION/EXPERIENCE

  • Bachelor’s Degree required, preferably in Science or related science field from an accredited college or university and minimum of 1 year experience required in related laboratory experience

SKILLS/KNOWLEDGE/ABILITIES

  • 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.
Responsibilities
  • 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
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