Join us at Industry X, where we are at the forefront of innovation, intelligence enhancement, and sustainability in manufacturing. We empower leaders to transition into a smarter, more connected, and sustainable future. At Industry X, you will collaborate with a recognized team dedicated to delivering rapid results, enabling clients to thrive amidst a dynamic industrial landscape.
In our Manufacturing & Operations practice, you'll be pivotal in transforming our clients' core manufacturing processes. Our specialists in Digital Production & Operations are committed to driving modernization through expertise in Execution Systems (MES/MOM), Automation, and Plant Data Models.
You Are:
A motivated Manufacturing Systems Specialist excited to embrace new challenges. As industries forge ahead with digitalization, your role in MES will be key to achieving manufacturing excellence.
Your Responsibilities:
- Lead the design, documentation, and implementation of Manufacturing Execution Systems (MES).
- Create and configure Electronic Batch Records (EBR).
- Implement MES solutions while ensuring seamless integration with ERP and control equipment.
- Document MES configurations and validate EBR processes.
- Provide oversight for complex systems related to MES development.
- Collaborate with business management and users to identify needs and design impactful solutions.
- Partner with clients to discover and implement optimal solutions.
- Guide teams in executing these tasks efficiently.
- Analyze business information needs for timely solution delivery.
- Gather user requirements for controlling and recording manufacturing activities.
- Respond to client proposal requests promptly.
- Nurture client relationships effectively.
- Oversee global system implementations.
- Manage small to medium teams and projects.
Travel Requirements:
Travel may range from 0 to 100% based on business needs and client requirements.
Job Requirements:
- At least 1 year of experience with Rockwell FactoryTalk PharmaSuite (FTPS) in a highly automated Life Sciences manufacturing environment.
- Bachelor's Degree or equivalent experience (minimum 3 years). For candidates with an Associate's Degree, a minimum of 6 years of relevant experience is expected.
Preferred Qualifications:
- Familiar with FDA and GMP guidelines.
- Understanding of Life Sciences validation processes.
- Working knowledge of the Software Development Life Cycle (SDLC) and support methodologies.
- Excellent communication skills, both written and oral.
- Able to work collaboratively in a team-oriented environment.
- Competent in facilitating meetings and following up on action items.
At Accenture, compensation varies and is influenced by numerous factors, including role. We continuously accept applications and encourage you to apply!
Accenture is committed to diversity and inclusion, ensuring equal employment opportunities while fostering a culture free of discrimination. We value each team member's individuality and strive to create an environment that sparks innovation and creativity.
If you require accommodation for the application process due to a disability or religious observance, please reach out to us. We are dedicated to ensuring accessibility for all candidates.
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