Quality Assurance Specialist
Company Name:
Teva Pharmaceuticals
The Quality Assurance Specialist conducts activities required of the Quality Assurance Department, including, but not limited to, audits, documentation maintenance, vendor qualifications and investigations. Ensures accuracy, proper documentation, and full compliance with approved methods, USP and cGMP''s.
Must not be allergic to penicillin.
1. Under minimal supervision and established guidelines, supervises and conducts cGMP related internal audits.
2. Assists departmental supervisors, managers and other more senior individuals with investigations, identifying errors and solving problems.
3. Assists as assigned with external audits (FDA, Vendors).
4. Maintains proper documentation and provides approval of Vendor Qualifications.
5. Demonstrates comprehensive understanding and use of technical standards, principles, theories, concepts and techniques for audit work as well as reviewing and writing SOP training guidelines associated with the groups'' job function.
6. Assists in maintaining regulatory compliance and a safe work area. Follows Teva Safety, Health and Environmental Policies and Procedures. Performs other duties as assigned or required by business needs.
7. Prepares annual reviews and assists in other regulatory submissions as assigned.
Bachelor''s Degree.
Four years'' experience in laboratory, quality assurance or related field.
Or, Master''s Degree with two year''s experience in laboratory, quality assurance or related field.
Pharmaceutical manufacturing experience preferred.
Date: 2014-06-26
Country: US
State: MO
City: Mexico
Postal Code: 65265
Category: Quality - Quality AssuranceEstimated Salary: $20 to $28 per hour based on qualifications.
Teva Pharmaceuticals
The Quality Assurance Specialist conducts activities required of the Quality Assurance Department, including, but not limited to, audits, documentation maintenance, vendor qualifications and investigations. Ensures accuracy, proper documentation, and full compliance with approved methods, USP and cGMP''s.
Must not be allergic to penicillin.
1. Under minimal supervision and established guidelines, supervises and conducts cGMP related internal audits.
2. Assists departmental supervisors, managers and other more senior individuals with investigations, identifying errors and solving problems.
3. Assists as assigned with external audits (FDA, Vendors).
4. Maintains proper documentation and provides approval of Vendor Qualifications.
5. Demonstrates comprehensive understanding and use of technical standards, principles, theories, concepts and techniques for audit work as well as reviewing and writing SOP training guidelines associated with the groups'' job function.
6. Assists in maintaining regulatory compliance and a safe work area. Follows Teva Safety, Health and Environmental Policies and Procedures. Performs other duties as assigned or required by business needs.
7. Prepares annual reviews and assists in other regulatory submissions as assigned.
Bachelor''s Degree.
Four years'' experience in laboratory, quality assurance or related field.
Or, Master''s Degree with two year''s experience in laboratory, quality assurance or related field.
Pharmaceutical manufacturing experience preferred.
Date: 2014-06-26
Country: US
State: MO
City: Mexico
Postal Code: 65265
Category: Quality - Quality AssuranceEstimated Salary: $20 to $28 per hour based on qualifications.
|
|
 | |
