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Validation Engineer in Fremont, CA at Integrated Resources, Inc

Date Posted: 12/7/2018

Job Snapshot

Job Description

Job Description
This hands-on role provides the opportunity to provide manufacturing and validation engineering support by performing validation/qualifications in support of the established site wide Validation Master Plan. This role is responsible for generating validation deliverables, executing validation or qualification documents, leading validation project teams and overall support of the validation project schedule.

Job Overview

Generate, execute and report on protocols for the qualification of facilities/utilities/equipment and validation of manufacturing processes.Assist in the development of user requirements for new equipment acquisitions and validation plans as well as generate validation lifecycle documents.Conduct validation or qualification tests of new or existing equipment.Conduct risk assessments for equipment and processes.Develop validation strategies based on regulatory requirements, scientific rationale, industry practice and assessed risk.Perform P&ID and I/O verifications.Participate in FAT, SAT, commissioning and startup of new equipment.Provide project updates to supervisor/manager. Escalate issues and provide recommendations for resolution.Assess the revalidation requirements for any equipment modifications or process changes.Provide input to the Facilities Department on preventive maintenance and calibration requirements, including setting appropriate calibration tolerances and frequency of calibration.Work with the Manufacturing and Quality departments to develop and train on standard operating procedures and work instructions.Handle multiple projects and work independently.

Requirements

Bachelor Degree in a field of science. Engineering degree is preferred.5 years of experience in the cGMP regulated industry. In-vitro diagnostic experience preferred.Demonstrated experience in facility/utility/equipment qualification and process validation.Skilled in the setup and calibration of a Kaye Validator for temperature mapping studies.Good understanding of ISO 13485 and FDA 820 requirements relating to product realization and process validation.Good analytical skills and ability to communicate effectively with all levels.Proficient in Microsoft Word and Excel.Good understanding of statistical techniques is a plus.Demonstrated validation project leadership skills.