Supervisor – QA Components

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 Supervisor ? QA Components.

 

Responsibilities:

* Supervise QA Component Technicians and Quality Analyst(s) and oversee the component lab daily activities to ensure priorities and deadlines are met and compliance to SOPs and cGMPs.

* Review and approve component incoming receiving inspection test results.

* Perform and monitor required training of personnel.  Assist in implementation of training programs.  Administer personnel performance evaluations.

* Interface with all departments to provide component and project support and to resolve quality issues.

* Analyze component quality issues and communicate with vendors through Vendor Corrective Actions to ensure resolution.

* Communicate with vendors to establish component specifications.  Develop/revise, review, and/or approve component specifications.  Coordinate the qualification of new components.

* Perform Quality investigations as it pertains to components.

* Develop, review, and/or approve documents such as SOP?s, CSCR?s, MCA?s, Component Specifications and Drawings (RMDS).

* Track and analyze vendor quality performance.  Summarize results in the Component Summary section of the Annual Product Review Report.

* Assist with the sampling and shipping of contract customer samples.

* Follow Teva Safety, Health, and Environmental policies and procedures. Other duties, as assigned, or as business needs require.

 

 Requirements:

* Education Required: Minimum 4-year degree in Science, or Engineering.

* Education Preferred: ASQC or Certified Quality Engineer (CQE/CQA).

* Experience Required: Minimum 3 years of pharmaceutical or related work experience.  Computer literate.  Good written and verbal skills.

* Experience Preferred: Quality or Production related experience in the Pharmaceutical, Medical Device, or Biotechnology industries.  Supervisory experience.

* Specialized or Technical Knowledge, Licenses, Certifications needed: Good understanding of cGMP regulations and their importance in compliance. 

 

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 #5119.  You may also fax your resume to 949-458-8945.