| Job description |
| Job description: |
Teva Parenteral Medicines is a global leader in the manufacture of generic injectable pharmaceuticals. A member of TEVA Pharmaceuticals Industries, the world's leading manufacturer and marketer of generic drugs. The company's mission is to play a leading role in the transformation of the U.S. healthcare system through its preeminence in the development, manufacture and marketing of generic pharmaceuticals.
- Prepares written defined validation/revalidation protocols under minimal direction of Validation engineer II or above, supervisor, or manager.
- Independently performs execution of validation protocols and/or revalidation standard operating procedures (SOPs).
- Prepares final reports and packages under direction of Validation engineer II or above, supervisor, or manager.
- Performs limited technical reviews and interprets data for accuracy of equipment/process performance for completed validations/revalidations.
- Writes, revises, and reviews SOPs related to validation/re-validation activities under minimal direction of Validation engineer II or above, supervisor, or manager.
- Ensure and/or executes proper calibration and maintenance of test equipment used for validation/revalidation of equipment and processes.
- Follows Teva Safety, Health, and Environmental policies and procedures.
- Other duties, as assigned, or as business needs require.
Primary Outcomes
- Validation and revalidation activities are completed on-time in accordance to regulatory and corporate requirements.
- Performs and coordinates individual tasks related to Validation work assignments and ability to communicate clearly and accurately the status to management.
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| Req. candidate profile : |
Education Required:
- Bachelor's degree in a Life Science/Engineering field.
- Experience Required: Minimum 1 year of experience performing validation activities or equivalent work experience in pharmaceutical manufacturing or related field.
- Experience Preferred: Minimum 3 years of experience performing validation activities in a parenteral manufacturing facility.
- Specialized or Technical Knowledge, Licenses
Certifications needed:
- Knowledge of good documentation practices, aseptic technique and Classified areas gowning procedures, required. Strong mechanical/technical skills. Good understanding of cGMPs.
- As a 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 Parenteral Medicines 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 # 07-1789. You may also e-mail your resume to Kavita.anand@tevausa.com or fax your resume to 949-458-8945.
- No relocation is offered for the position. Only local candidates will be considered. Resumes will be reviewed and qualified candidates will be contacted for pre-screening
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| How to apply : |
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| Third party mediation allowed : |
No |
| Telecommute : |
No |
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