Validation Engineer 005

Write Commissiong, Qualification and Validation (C/Q/V) documents following established standards and templates. Perform field/site validation activities. C/Q/V of equipment and systems, including CSV and automation, supporting pharmaceutical, biotech, and medical device industries. Read, understand and utilize the Best Practices and SOPs for delivery of compliance services. Perform work to meet budget requirements and quality standards. Provide consistent, complete, and timely feedback and reports to project leaders, project managers, or management, of project status and issues, as requested. Travel and/or Relocation to various unanticipated locations throughout the US required. The purpose of travel and/or relocation would be to work with clients on projects. The frequency of travel and/or relocation will be determined by the needs of clients. Apply knowledge of the following: Execution of Test Protocols, managing validation document development process, manufacturing of medicines/vaccines/diagnostic products.

Position requires a Bachelor’s Degree in Pharmaceutical Sciences or a related field and twelve (12) months experience. One (1) year experience must have included: Execution of Test Protocols, managing validation document development process, manufacturing of medicines/vaccines/diagnostic products. Travel and/or Relocation to various unanticipated locations throughout the US required. The purpose of travel and/or relocation would be to work with clients on projects. The frequency of travel and/or relocation will be determined by the needs of clients. 

To apply, please send resume and cover letter referencing ref. # 474.005 to: pramod@advancedhealthinformatics.com or by U.S. Postal Mail to: ADVANCED HEALTH INFORMATICS, LLC, 8628 Industrial Parkway, Suite E, Plain City, Ohio 43064.