1+ months
Company Info

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

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!

Job Description

Under close supervision, carries out laboratory work to support method investigations, method validations, method transfers, and method comparisons. Performs laboratory analyses using general laboratory equipment and techniques per established procedures and approved protocols, including standard and sample preparation, operation of analytical instruments, and documentation of results following proper cGMP procedures.
Essential Job Functions:

Carries out responsibilities in accordance with the organizations policies, procedures, and state, federal        and local laws.
Performs qualitative and quantitative analyses in support of method investigations and method validations following approved protocols.
Interprets analyses findings, identifies and reports on technique differences at various stages of the analytical process impact the results.
Performs qualitative and quantitative analyses in support of method transfers and method comparisons following established procedures and approved protocols.
Utilizes and operates general laboratory equipment such as balance, pH meter, IR spectrometer, UV/VIS spectrometer, HPLC and dissolution apparatus for standard and sample   preparation.
Conducts wet chemistry tests as needed, including, TLC, LOD, titration, particle size, disintegration, hardness and friability. Interprets and may report on results.
Prepares tables, spreadsheets and graphs following protocols and/or instruction of senior colleagues.
Carries out cGMP and technical training, as it pertains to area of work.
Meets project deadlines and performance standards as assigned.
May develop, write and review new procedures, test methods and specifications documents. May also update existing procedures, test methods and specifications documents.
Ensures compliance with all Company policies and procedures, including safety rules and regulations.
Performs related duties as assigned.



Bachelors Degree in Chemistry or related science field from an accredited college or university, and one (1) year related laboratory experience or an equivalent combination of education and experience. cGMP experience a plus

Knowledge of:

Current Good Manufacturing Practices (cGMP), Food and Drug Administration (FDA), and other regulatory requirements.
Pertinent SOPs related to pharmaceutical laboratory testing, analyses and documentation.
Basic analytical techniques, including weighing, pipetting, etc.
UV/IR, HPLC, GC and TLC instruments operation methods and techniques.
Business, scientific and personal computer hardware and software applications.
Basic math skills needed to use basic chemical equations, calculate concentrations, and determine weight and/or volumes for scale-ups or scale-downs.
Wet Chemistry and Chemistry related to sampling methods, quality control systems, analysis and documentation practices and procedures.
FDA, cGLP, cGMP, and SOP regulatory rules, regulations and guidelines.
Spectroscopic and chromatographic operation, techniques and systems.
Dissolution testing.
Current Company policies, practices and procedures, including safety rules and regulations.

Skill in:

Performing testing accurately and precisely.
Responding to routine inquiries from management, employees and regulatory agencies.
Communicating clearly and concisely, both orally and in writing.
Operating scientific and personal computers.

Sub Function
Manufacturing Quality Control
Reports To
In process of validation
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: 2020-06-30 Expires: 2020-09-06

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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LTS Scientist I

Teva Pharmaceuticals

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