Senior MES Manager (Syncade) – Life Sciences

Accenture

Chicago (IL)

Remote

USD 87,000 - 254,000

Full time

10 days ago
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Job summary

Accenture seeks an ambitious Manufacturing Systems (MES) Manager to drive design, development, documentation, and deployment of Emerson Syncade MES in a highly automated Life Sciences environment. You will implement MES solutions, integrate with ERP and control systems, and ensure EBR validation while collaborating with business leaders to define needs and deliver valuable solutions.

The role requires deep knowledge of FDA/GMP guidelines, strong English communication, and the ability to work in

Qualifications

  • 5+ years of Emerson Syncade MES experience in automated Life Sciences manufacturing.
  • Knowledge of FDA and GMP guidelines is essential.
  • Strong written and oral communication skills in English.
  • Ability to work in a team-oriented environment and lead meetings.
  • Experience converting Life Sciences processes into electronic batch records.

Responsibilities

  • Lead design, development, documentation, and implementation of MES Design/Author/Develop/Configure EBR.
  • Implement MES solutions and integrate with ERP and control equipment.
  • Document MES configuration and validate electronic batch records.
  • Collaborate with management and users to define needs and design value-adding solutions.
  • Document and analyze business information needs to ensure compliant solutions.
  • Support go-live and hypercare activities for MES deployments.
  • Manage client relationships and respond to proposals.

Skills

Emerson Syncade MES
FDA GMP knowledge
English proficiency
Teamwork
SDLC familiarity

Education

Bachelor's degree or equivalent
Associate degree with 6 years experience

Job description

Accenture seeks an ambitious Manufacturing Systems (MES) Manager to drive design, development, documentation, and deployment of Emerson Syncade MES in a highly automated Life Sciences environment. You will implement MES solutions, integrate with ERP and control systems, and ensure EBR validation while collaborating with business leaders to define needs and deliver valuable solutions.

The role requires deep knowledge of FDA/GMP guidelines, strong English communication, and the ability to work in

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