Analytical Chemist II

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.

The opportunity

The Quality Control Laboratory Analytical Chemist II is responsible to work independently with minimal or no supervision under the direction of the QC Manager/Chemist 5 performing analytical testing dealing with moderately complex chemical and physical analyses associated with commercial production and stability samples. As an Analytical Chemist 2, responsibilities also extend to providing technical and analytical support when necessary to the QC Laboratory.

How you’ll spend your day

Tasks and responsibilities will include but are not limited to:

 

• Performs analytical testing of materials associated with commercial production and stability samples.
• Assists with the execution and completion of analytical investigations carried out by QC Laboratory as required.
• Assists in the new technology implementation as required.
• Performs all planning functions that are integral to the overall operation of the laboratory and in so doing, ensures that execution of work can be carried out in most cost effective and productive manner.
• Performs all QC project management activities associated with new product launches, alternate sourcing, site transfer and, other company initiatives as they relate to cost savings and continuous improvement.
• Performs other related duties as required
   

Your experience and qualifications

• College Diploma or University Degree in Chemistry or a related science.
• 2+ Years Laboratory Experience
• LIMS (Laboratory Information Management System), CDS (Chromatography Data System), Trackwise, MSOffice.
• Knowledge of, and experience in a Quality Control Laboratory and working knowledge of GMP/cGMP as they pertain to QC laboratory unit.
   

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.