Validation Specialist
Where
- Queensbury, NY
What you'll be doing
- The client company is seeking a Validation Specialist for a growing company in the Queensbury area. This position is responsible for ensuring requirements for ISO and QSRs are met. Providing data to management for all aspects of customer validation project. Effectively communicating with other departments and facilities as well as customers. Planning, organizing and coordinating all customer validation activities. Writing validation protocols, collecting and analyzing data, executing validation protocols using various methods and providing training on any validation issues. Ensuring that all validation activities are performed according to the client QSR. Additional duties as assigned.
What your background should be
- An ideal candidate must have 3 years experience performing similar duties and minimum 2 years experience in pharmaceutical, food or medical device industry. Understanding of US FDA quality system regulations and ISO 9000 regulations. Experience and knowledge with US and International requirements for medical devices. Background in good manufacturing practice (GMP). Experience with technical writing and executing validation protocols. Proficiency with computer programs including Microsoft Office.
Required Schooling / Training
- Bachelor Degree in science related field.
Who is the client company
- A multinational human resource consulting firm that provides recruitment and assessment, training and development, career management, outsourcing, and workforce consulting.
- If you are interested in this position, send your resume to apply@kochdavis.com
