MES Specialist - Life Sciences (Apprentice.io)

Accenture PLC

San Diego (CA)

Remote

USD 42,000 - 136,000

Full time

9 days ago

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Job summary

Accenture is seeking an ambitious Manufacturing Systems (MES) Specialist to join our team. You will lead the design, development, documentation, and implementation of Apprentice.io MES within a highly automated Life Sciences manufacturing environment.

You will also design, configure and validate Electronic Batch Records (EBR), integrate MES with ERP and control equipment, and collaborate with management and users to define needs and deliver value while adhering to FDA and GMP guidelines.

Qualifications

  • Minimum 3 years of experience with Apprentice.io MES solutions in a highly automated Life Sciences manufacturing environment.
  • Bachelor’s Degree or equivalent (minimum 3 years work experience). If Associate’s Degree, must have equivalent minimum 6 years work experience.
  • Knowledge of FDA and GMP guidelines.

Responsibilities

  • Lead in the design, development, documentation, and implementation of Apprentice.io 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 with management and users to define needs and design value-adding solutions.
  • Document and analyze business information needs to deliver compliant solutions.
  • Respond to client proposals and manage client relationships.

Skills

MES Specialist
FDA and GMP knowledge
Team collaboration

Education

Bachelor’s Degree or equivalent

Tools

Apprentice.io MES

Job description

Accenture is seeking an ambitious Manufacturing Systems (MES) Specialist to join our team. You will lead the design, development, documentation, and implementation of Apprentice.io MES within a highly automated Life Sciences manufacturing environment.

You will also design, configure and validate Electronic Batch Records (EBR), integrate MES with ERP and control equipment, and collaborate with management and users to define needs and deliver value while adhering to FDA and GMP guidelines.

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