工作描述
Are you a motivated Systems Engineer with Manufacturing Execution Systems (MES) experience within the Life Science, Pharmaceutical or Biotech industry? Are you passionate about driving forward innovation in manufacturing excellence, and helping leading organizations to move towards Manufacturing and Factory Digitalization? Would you like to accelerate your career and join our growing team of MES experts?
We are looking for an ambitious Manufacturing Execution Systems Engineers with hands-on MES design experience ready to take on new challenges, joining our teams in Cork and Dublin. This opportunity will see you join an industry leader in deployment of Manufacturing Systems for the Life Science Manufacturing industry.
Our global teams partner with some of the world’s leading life science companies, offering professional engineering and consulting services (strategy, plan, design, deploy and sustain) for Manufacturing and Supply Chain Operations. We leverage our deep MES, Validation, and Data Analytics skills, combined with Accenture’s core capabilities and digital enablers, to transform manufacturing and supply chain operations for pharmaceutical, biotech and medical device clients globally.
As a MES Technical Consultant, you will:
Partner with technical leads and clients to support the design, development, documentation, and implementation of Manufacturing Execution Systems (MES) for a growing client base
Collaborate with business clients and internal teams to determine appropriate solutions and deliver on multiple large-scale projects
Work collaboratively with business users to define the needs and design solutions that add value
Gather user requirements in relation to controlling and recording manufacturing activities
Design, author, develop and configure Electronic Batch Records (EBR)
Implement MES solutions and integrate with ERP and control equipment
Document MES configuration and validation of EBRs
职位要求
What we are looking for:
Bachelor’s degree in science, Engineering or relatable technical degree
Strong hands-on MES experience (typically 3-5 years'), gained in a highly automated Life Sciences manufacturing environment
Experience with at least one of the following: Korber PAS|X, Emerson Syncade, Rockwell PharmaSuite, Siemens XFP, POMS, Camstar or other life sciences compatible MES solutions
Working knowledge of FDA and GMP guidelines and of Software Development Life Cycle (SDLC) and support methodologies required
Team-oriented, with strong communication skills and evidence of success working in a collaborative life sciences, biopharma or biotechnology environment
#LI-EU
