Validation Engineer II
Join one of the world's fastest growing pharmaceutical companies!
At Allergan you will have the opportunity to thrive in a fast-paced, strategic environment where bold, innovative thinking isn't just welcomed, it's encouraged. Across all functions, we relish the opportunity to help our people fulfill their potential. Our rapid growth strategy means plenty of opportunities to step into the spotlight.
Position Description
The Validation Engineer is responsible for but not limited to, working under operations Integration department in developing and implementing product, process, and equipment, and validation protocols, as applicable to ensure compliance to applicable regulatory requirements, internal company standards and industry practices. As a member of Operation/Validation team, responsible for developing /supporting of revenue and process improvement projects and executing IQ/OQ/PQ/PPQ protocols and making recommendations for changes and/or improvements. Ensure project completion per schedule, overall compliance and continuous quality and product/process improvement in an ever-changing, regulated environment.
Main Areas of Responsibilities
• Develop, write and execute validation protocols (IQ/OQ/PQ/PPQ, etc.), test scripts and specifications for equipment, systems, products and processes, including required annual re-qualifications and writing validation plans and final validation reports.
• Work with Sr. Validation Engineer & Manager for validation services and other Operation Engineering and Quality Management in the development of validation master plans to fulfil requirements of the current Good Tissue Practices regulations (21 CFR 1271), Medical Devices – Quality System Regulations (21 CFR 820), ISO 13485 and other applicable regulations…cont.
-See more at http://www.hirelifescience.com/validation-engineer-ii/branchburg-nj-11111-720923/?p=p&submission=2
