Job Description :
Description:
Develops, publishes, and implements test plans. Writes and maintains test automation.
Develops quality assurance standards. Defines and tracks quality assurance metrics such as defect densities and open defect counts.
Requires a bachelor''s degree and 4-7 years of experience coding in C, C++, Java.
Must have a working knowledge of quality assurance methodologies. Familiar with NT, UNIX and/or Solaris environments.
Generally, supports commodity or generic/unspecified skills, such as R&D Domain and SharePoint Testing.
Relies on experience and judgment to plan and accomplish goals. Performs a variety of tasks.
Works under general supervision; typically reports to a manager. A certain degree of creativity and latitude is required.
Required:
The resource will perform validation testing for GMP systems at Pharmaceutical’s.
Resource must have 5+ years of experience authoring and executing validation protocols for GMP systems.
Good communication skills are required, with the ability to successfully interact with project team and validation team members.
Experience authoring and executing validation protocols for GMP systems
Be flexible in the validation approach (as it’s not a one-size fits all model), accept feedback, and adjust
Good working knowledge of CFR 21 Part 11