27 days old

LTS Scientist II

Salt Lake City, UT 84111
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

 

Under general supervision, carries out laboratory work to support somewhat complex method investigations, method validations, method transfers, and method comparisons. Under the direction of senior colleagues, performs non-routine testing, such as evaluation of USP proposals/revisions and reference standard qualifications.


Essential Job Functions: This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all duties listed, and may be required to perform additional, position-specific tasks.


    Carries out responsibilities in accordance with the organizations policies, procedures, and state, federal and local laws.
    Performs qualitative and quantitative analyses in support of complex method investigations and method validations following approved protocols.
    Interprets analyses findings, identifies and reports on how technique differences at various stages of the analytical process impact the results.
    Conducts non-routine testing such as evaluation of USP proposals/revisions, routine cleaning validation testing and reference standard qualification.
    Performs qualitative and quantitative analyses in support of method transfers and method comparisons following established procedures and approved protocols.
    Involves standard and sample preparation; the operation of general laboratory equipment such as balance, pH meter, IR spectrometer, UV/VIS spectrometer, HPLC and dissolution   apparatus.
    Performs more advanced analyses, which require a higher level of technical skill and knowledge (e.g., AA spectrometry, GC).
    Manages wet chemistry tests as needed, which may include TLC, LOD, titration, particle size, disintegration, hardness, and friability.
    Writes protocols and reports to support method investigations/method validations and performs data calculations with PC applications and specialized lab (instrument) applications.
    Performs basic troubleshooting of instruments/equipment.
    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.

Qualifications

 

Minimum Qualifications:

 

Bachelors Degree in Chemistry or related science field from an accredited college or university, and three (3) years related laboratory experience; or an equivalent combination of education and experience. Pharmaceutical experience a plus

Function
Quality
Sub Function
Manufacturing Quality Control
Reports To

Manager, Quality Control 

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.

Categories

Posted: 2020-09-24 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.

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

LTS Scientist II

Teva Pharmaceuticals
Salt Lake City, UT 84111

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast