" Recipe Authoring using Syncade MES

" Execute test scripts (design, execution, simulation, wet testing).

" Own change requests and complete change request tasks to support project completion.

" Perform change request assessments.

" Deviations / Root Cause Analysis (RCAs).

" Assist the Quality department with deviation investigations.

" Assist with completion of CAPA actions.

" Participates in quality risk assessments.

Documentation

" Review/revise automation and Manufacturing related SOP's, Functional Specifications, and work instructions, equipment/process changes, error prevention activities, etc.

" Author and review test protocols.

" Perform other duties as assigned.

Key Requirements:

" Bachelor's degree in an engineering or related discipline.

" Related work experience in a GMP environment.

" Strong communication and leadership skills.

" Ability to secure relevant information and identify key issues and relationships from a base of information.

" Ability to evaluate engineering problems and be able to devise cause and effect relationships and propose solutions.

" Ability to fulfill on-call hours requirements.

" MES Syncade Recipe Authoring experience.

" VBA coding or Interface experience is plus.