PAS-X MES Consultant | Manufacturing Digitalization Expert

Accenture; San Diego (CA); On-site; USD 43,000 - 136,000; Full time

Job summary

Accenture seeks an ambitious Manufacturing Systems (MES) Specialist to design, develop, and validate Körber PAS-X MES in highly automated Life Sciences environments. You will implement MES, author Electronic Batch Records, and integrate MES with ERP and control equipment.

Travel may be required. Requires 2+ years PAS-X MES experience, plus FDA/GMP knowledge, strong communication, teamwork, and SDLC proficiency. A Bachelor’s Degree or equivalent is expected.

Qualifications

• Knowledge of FDA and GMP guidelines
• Strong written and oral communication skills
• Ability to work in a team-oriented, collaborative environment
• Ability to facilitate meetings and follow up with resulting action items
• Understanding of Life Sciences validation processes
• Working knowledge of SDLC and support methodologies
• Bachelor’s Degree or equivalent (minimum 3 years work experience). If Associate’s Degree, must have equivalent minimum 6 years work experience

Responsibilities

• Lead in the design, development, documentation, and implementation of Körber PAS-X MES
• Design/Author/Develop/Configure Electronic Batch Records (EBR)
• Implement MES solutions and integrate with ERP and control equipment
• Documentation of MES configuration and validation of EBRs
• Work closely with business management and users to strategically define the needs and design solutions that add value
• Document and analyze the information needs of the business and ensure appropriate solutions are delivered according to GxP standards
• Respond to requests for client proposals
• Manage and develop client relationships

Skills

Körber PAS-X MES

Life Sciences

Team collaboration

SDLC knowledge

Education

Bachelor’s Degree or equivalent (minimum 3 years work experience)

Tools

ERP integration

Job description

Accenture seeks an ambitious Manufacturing Systems (MES) Specialist to design, develop, and validate Körber PAS-X MES in highly automated Life Sciences environments. You will implement MES, author Electronic Batch Records, and integrate MES with ERP and control equipment.

Travel may be required. Requires 2+ years PAS-X MES experience, plus FDA/GMP knowledge, strong communication, teamwork, and SDLC proficiency. A Bachelor’s Degree or equivalent is expected.