Investigative Reviewer/ Quality Assurance

Position Type: Full-Time

About Us:
Teva Pharmaceutical Industries Ltd. is a global pharmaceutical company specializing in the development, production and marketing of generic and proprietary branded pharmaceuticals as well as active pharmaceutical ingredients. Teva is among the top 20 pharmaceutical companies and is the largest generic pharmaceutical company in the world.

Responsibilities:
Perform batch record review and product releases for packaging and distribution under moderate supervision.
Perform manufacturing investigations under moderate supervision.
Promote conformance to GMP's and FDA Regulations.
Remain current with all pertinent standard operating procedures relating to batch record review and QA systems.
Other responsibilities as assigned by the QA Management.
REQUIREMENTS
Requirements:
Bachelor's degree minimum (science degree referred), with pharmaceutical or QA/QC experience preferred.
Non-degreed candidates with at least eight years of appropriate pharmaceutical and QA/AC experience, or equivalent combination of education and experience.
Basic computer skills - MS Word, Excel, Lotus Notes, Access.
Ability to effectively present information verbally and in writing to peers, immediate supervisor and work groups.
Works under direct supervision.
Ability to participate in a team based organization and a willingness to actively participate in team meetings.
Ability to provide solutions to a variety of quality and technical problems of limited scope and complexity.
Ability to effectively negotiate a best solution for issues of limited scope.~CB