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 position will support QC laboratory testing and compliance related activities. The candidate will perform sampling, testing and release of raw materials and in process testing. Additional responsibilities and duties will include compendia testing in support of GMP samples and development studies. The incumbent should possess a practical understanding of GMP requirements within a QC laboratory environment. This is an entry level analytical laboratory position requiring 1-2 years of relevant experience within the pharmaceutical industry. The position requires independence, technical expertise, ability to perform routine work following written procedures and ability to work on multiple projects.

How you’ll spend your day

• Maintain compliance with applicable ICH, GLP, GMP and safety regulations. Notify management of unexpected results, procedural deviations and equipment problems.
• Perform testing as per current approved test method and maintain accurate laboratory records and adhere to cGMP/GDP expectations.
• Perform sampling, testing and release of raw materials and in process testing.
• May perform non-compendia analytical testing (e.g., chromatography).
• Participate in the writing/editing of standard operational procedures, forms and reports and data archiving as requested.
• May participate in laboratory investigations change controls.
• Assist with sample maintenance as requested.
• Maintain a collaborative working relationship with QC staff and other Teva departments (Quality Assurance, Analytical Development).
• Record data per GxP requirements. Provide peer review of documentation as needed.
• Actively contribute to the maintenance of a clean, safe working environment in the laboratories.

Your experience and qualifications

• At least 1 year of experience in GMP pharmaceutical environment.
• Bachelor’s degree in scientific discipline (Chemistry, Biochemistry, Biology)

Enjoy a more rewarding choice

Make a difference with Teva Pharmaceuticals

Reports To

Senior Manager Quality Control, Biologics CMC

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.

Important notice to Employment Agencies - Please Read Carefully

Teva Pharmaceuticals USA does not accept unsolicited assistance from agencies for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.