Qc Associate Jobs

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

Working independently under the supervision of the QC Laboratory Supervisor. The incumbent having an advanced knowledge of analytical chemistry (USP/NF, BP/EP) and GMP/cGMP testing requirements, coordinates audits and performs release activities associated with all analytical testing (Raw Materials, Finished Products, Stability, Packaging Components, Microbiology), calibration records performed in the Quality Control Laboratory. In addition, the incumbent will be required complete usage decision in SAP for Raw Material and Excipients and the preparation of data integrity reports for QC Lab instrumentation where applicable.

• Audits all electronic records in LIMS and Empower prior to authorizing components in LIMS and update in SAP.
• Responsible for the final analytical release assessment of raw materials, finished products, packaging components and stability samples.
• Responsible for electronic signature audit entries made in the Laboratory Information Management System (LIMS), Empower and SAP.
• Coordinates and ensures that all the applicable documentation related to the testing of a project are compiled and organized prior to releasing and filing of the analytical documentation.
• Reviews and checks analytical reports, calculations, chromatograms and printouts related to all types of QC Lab testing such as RM, FP, stability, packaging and microbiological testing by ensuring that work by the lab has been carried out in accordance with specifications, applicable analytical methodology, SOP and the GMP/cGMP’s.
• Responsible for generating/revising applicable documentation Standard Operating Procedure, GLP, IA/T and analytical templates..

Your Experience And Qualifications

• Minimum of 3 years experience as a QC Assocaite.
• Anticipate consequences; negotiate solutions to address various concerns.
• In depth knowledge of laboratory procedures, instrumentation, USP/NF, BP/EP and investigations.
• Demonstrate the ability to prioritize, analyze, plan, implement, and adjust goals and objectives to meet needs.
• Accomplish moderately complex tasks simultaneously.
• Product Knowledge, Laboratory compliance standards.
• Required to work independently and follow through on assignments/instructions/tasks with minimal supervision/direction.
• Minimum Community College or University Degree in Chemistry or related field.
• Community College or University Degree in Chemistry or related field (preferred).
• Laboratory Information Managements system (LIMS), Empower, SAP, Laboratory Instruments.

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.

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, genetic information, marital status, sexual orientation, gender identity or expression, ancestry, national or ethnic origin, citizenship status, military status or status as a disabled or protected veteran, or any legally recognized status entitled to protection under applicable federal, state, or local laws.