Auditor I/II

Teva Sicor Pharmaceuticals is a global leader in the manufacture of generic injectable pharmaceuticals. Now a member of TEVA Pharmaceuticals Industries, the world's leading manufacturer and marketer of generic drugs, TEVA Sicor has an excellent opportunity for Auditor I/II.

This position will be responsible for reviewing and approving R&D data and reports related to regulatory submissions to ensure data validity, integrity, and that they meet cGMP requirements.


Responsibilities:
* Review and approval of R&D laboratory notebooks to assure adherence to procedures (SOP’s), cGMP’s, and to ensure data validity and integrity.
* Review of R&D reports and laboratory documentation for data validity and integrity.
* Follows Teva Safety, Health, and Environmental policies and procedures.
* Other duties, as assigned, or as business needs require.
REQUIREMENTS
Requirements:
* Education Required: Bachelor’s degree or higher in a scientific field or equivalent combination of education and related experience.
* Education Preferred: Bachelor’s degree Chemistry
* Experience Required: Minimum 3 years auditing or compliance experience. Experience with HPLC, GC and other laboratory instrumentation. Knowledge of cGMP’s and Good Documentation Practices.
* Experience Preferred: 2+ years laboratory experience. 3+ years auditing experience. Experience in method development/validation.

As a new member of TEVA Pharmaceutical Industries, Ltd., the world's leading manufacturer and marketer of generic drugs, we regularly seek dedicated and hardworking professionals with the necessary skills for our business.

TEVA Sicor offers a comprehensive benefit package, including major medical, dental, vision, 401(k) and the opportunity to grow with a dynamic company. For immediate consideration, please visit www.tevausa.com. Click Employment Opportunities, then Positions Available and search for Position # 5190. You may also fax your resume to 949-458-8945.