
Quality Analyst Engineer
Review and oversee validations activities for process packaging performance qualifications to support product transfers and new product launches These activities include change controls, protocols, deviations and reports. Review and oversee qualification activities for equipment, facilities and utilities. These activities included SDLC documentation, change controls, protocols, reports and deviations. Review GxP assessments for equipment and systems Review and approval of periodic reviews for manufacturing equipment and systems, including temperature mapping studies for Sunrise and Davie facilities Review data to assure conformance to product specifications and maintains quality assurance objectives to meet corporate policies and goals. Ensure project deadlines and performance standards are established and met. Responsible for maintaining work areas and performing job functions in a safe and efficient manner in accordance with company policies and procedures, Good Manufacturing Practices (cGMP’s), Standard Operating Procedures (SOP’s) and Batch Record instructions.
Ability to sometimes work independently, multi-task and manage timelines.
Minimum of 7 years relevant experience in the pharmaceutical, medical device, or biotechnology industry
MS Word
Time Management Skills
MS Excel skills
SharePoint skills
MS PowerPoint Skills
Project planning/execution skills
SDLC documentation
Motivated, self-directed and driven
Problem-Solving
Strong organizational skills
Flexibility/Adaptability
Attention to detail and accuracy
Verbal and Written Communication
Multi tasker
According to JobzMall, the average salary range for a Quality Analyst Engineer in 4001 SW 47th Ave, Davie, FL 33314, USA is between $50,000 and $90,000 per year. Salaries for this position vary based on a variety of factors, including experience, education, industry, and location. The job duties of a Quality Analyst Engineer may include creating and reviewing quality assurance plans, developing and executing tests, analyzing test results, and providing feedback to engineering teams. Additionally, Quality Analyst Engineers may be responsible for developing quality assurance processes and procedures, providing technical support, and troubleshooting issues.
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Teva Pharmaceutical Industries Ltd., also known as Teva Pharmaceuticals, is an American Israeli pharmaceutical company with dual headquarters in Petah Tikva, Israel and Parsippany, New Jersey, U.S. Teva Pharmaceutical Industries Ltd. engages in the provision of pharmaceutical services. It operates through the following business divisions: Generic, Specialty Medicine, and Over-the-Counter (OTC).

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