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MES Engineer

Katalyst Healthcares and Lifesciences

Phoenix, Arizona • Today

Full-time

MES Engineer (Remote) - Ignition Certified Expired also fine

S3 Staffing USA

Remote • 3d ago

Easy Apply

Full-time, Third Party

50 - 70

MES Software Engineer

ElevaIT Solutions

Remote or Charlotte, North Carolina • Today

Contract

$82.00

Lead SAP MES Consultant

Visionaire Partners

Hybrid in Chandler, Arizona • 5d ago

Contract

$75 - $105

APRISO MES Consultant

Rcube IT llc

Remote • 30+d ago

Easy Apply

Contract

80+

SAP Apriso MES Consultant - Remote

Data Wave Technologies Inc

Remote • Today

Easy Apply

Contract

MES Lead

Indotronix International Corp

Remote • 19d ago

Easy Apply

Contract

Camstar MES Solution Architect

Axiom Global Technologies, Inc.

Remote • 2d ago

Easy Apply

Contract, Third Party

Depends on Experience

MES Architect

Augusta Hitech Soft Solutions LLC

Remote • 24d ago

Easy Apply

Contract

Depends on Experience

OpCenter MES Solution Architect - Remote

Amtex System Inc.

Remote • 4d ago

Easy Apply

Third Party, Contract

Depends on Experience

MES OCM Subject Matter Expert Analyst

Accede Solutions Inc

Remote • 26d ago

Easy Apply

Contract

70 - 90

MES Solution Architect

PDDN Inc

Remote • Today

Easy Apply

Full-time, Part-time, Third Party, Contract

Remote with Travel // Manufacturing MES Lead with Siemens Opcenter

Talent Groups

Remote • 9d ago

Easy Apply

Third Party, Contract

Depends on Experience

MES Project Manager - Remote || W2 only

Cerebra Consulting Inc

Remote or Lodi, California • Today

Easy Apply

Contract

Job Details

Skills

Workflow
Root Cause Analysis
Enterprise Resource Planning
LIMS
OPC
RESTful
Data Visualization
Decision-making
Dashboard
Management
Reporting
Technical Support
Manufacturing Execution System
Onboarding
Manufacturing Operations
Documentation
GDP
Data Integrity
Computer Science
Pharmaceutics
Biotechnology
GxP
GAMP
Computerized System Validation
MES
SQL
Python
C#
Manufacturing
System Integration
Conflict Resolution
Problem Solving
Analytical Skill
Effective Communication
Collaboration
Regulatory Compliance

Workflow
Root Cause Analysis
Enterprise Resource Planning
LIMS
OPC
RESTful
Data Visualization
Decision-making
Dashboard
Management
Reporting
Technical Support
Manufacturing Execution System
Onboarding
Manufacturing Operations
Documentation
GDP
Data Integrity
Computer Science
Pharmaceutics
Biotechnology
GxP
GAMP
Computerized System Validation
MES
SQL
Python
C#
Manufacturing
System Integration
Conflict Resolution
Problem Solving
Analytical Skill
Effective Communication
Collaboration
Regulatory Compliance

Summary

Summary:
The MES Engineer will play a critical role in supporting the design, development, implementation and management of the Manufacturing Execution Solutions (MES) within the organization's Drug Product manufacturing area. This role involves translating manufacturing processes into robust MES solutions, ensuring compliance with GxP standards, and integrating MES with other enterprise systems and automation platforms to streamline operations.
Roles & Responsibilities:

ssist in the design and configuration of Tempo MES solutions, including electronic batch records (eBRs), under the guidance of senior engineers.
Contribute to the development of modular, scalable, and reusable MES recipe templates based on ISA 88/95 standards.
Perform impact assessments for recipe modifications and system updates, ensuring adherence to GxP requirements.
Collaborate with cross-functional teams to gather user requirements and define functional specifications for MES functionalities.
ssist in recipe design and authoring electronic batch records (eBR) to develop modular, scalable and reusable MES recipe and equipment workflow templates following ISA 88/95 standards.
Perform root cause analysis and resolve MES issues related to system configuration, recipe design, or integration failures.
Support efforts to integrate MES with other enterprise systems, such as ERP, LIMS, and automation platforms, using industry-standard protocols like OPC or RESTful APIs.
ssist in the development of data visualization tools and reporting dashboards to support operational decision-making.
Possess technical knowledge in DCS, automation, and systems integration, including the design and management of data dashboards, label management systems, and reporting tools.
Provide day-to-day technical support for MES system users, assisting in troubleshooting and resolving recipe or system-related issues.
Participate in technical transfer activities to ensure smooth onboarding of new products and processes into manufacturing.
Support off-hours manufacturing operations as needed to address critical MES-related issues.
Ensure compliance with Good Documentation Practices (GDP), GxP regulations, Data Integrity guidelines and company policies during all MES-related activities.
Participate in validation activities to support the implementation and ongoing maintenance of MES systems.

Required Qualifications:

Bachelor's degree in Engineering, Computer Science, or a related technical field.
2-4 years of experience with MES systems, preferably some in Drug Product manufacturing in pharmaceutical or biotechnology environments.
Basic understanding of GxP regulations, GAMP guidelines, and Computer System Validation (CSV).
Exposure to MES platforms such as Tempo, Syncade, or equivalent systems is preferred.
Familiarity with basic programming concepts or languages like SQL, Python, or C#.
General knowledge of manufacturing processes, automation systems, and systems integration principles.
Strong problem-solving and analytical skills with a willingness to learn and adapt quickly.
Effective communication and collaboration abilities to work in cross-functional teams.
Commitment to maintaining compliance with regulatory and internal standards

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91116760
Position Id: 1fd832d1951c539f3d13b9c1403ee661
Posted 2 days ago

Fitment

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MES Engineer

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Summary: The MES Engineer will play a critical role in supporting the design, development, implementation and management of the Manufacturing Execution Solutions (MES) within the organization's Drug Product manufacturing area. This role involves translating manufacturing processes into robust MES solutions, ensuring compliance with GxP standards, and integrating MES with other enterprise systems and automation platforms to streamline operations. Roles & Responsibilities: Assist in the design a

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MES Solution Architect

Remote

•

Today

Role name: MES Solution Architect Work Location: United States (Remote) Start date: Immediate availability. Type: Contract Interview: Phone/Video At a high level, we're looking for: Strong Siemens Opcenter (Camstar) solution architecture and deployment experience Experience defining MES solutions and integrating with ERP, APS, equipment controls, and other manufacturing systems Hands-on knowledge of Opcenter Portal/Portal Studio, with additional Opcenter products being a plus Technical

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Remote

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9d ago

Remote with Travel Manufacturing MES Lead with Siemens Opcenter Contract Job description: Responsibilities: Lead functional and technical design of Siemens Opcenter MES solutions. Gather business requirements and translate them into MES workflows and configurations.Configure production, quality, genealogy, traceability, WIP, and electronic work instructions.Integrate MES with SAP ERP, PLM, equipment, automation, and shopfloor systems.Support testing, deployment, commissioning, and user training

Easy Apply

Third Party, Contract

Depends on Experience

Job Details

Skills

Workflow
Root Cause Analysis
Enterprise Resource Planning
LIMS
OPC
RESTful
Data Visualization
Decision-making
Dashboard
Management
Reporting
Technical Support
Manufacturing Execution System
Onboarding
Manufacturing Operations
Documentation
GDP
Data Integrity
Computer Science
Pharmaceutics
Biotechnology
GxP
GAMP
Computerized System Validation
MES
SQL
Python
C#
Manufacturing
System Integration
Conflict Resolution
Problem Solving
Analytical Skill
Effective Communication
Collaboration
Regulatory Compliance

Workflow
Root Cause Analysis
Enterprise Resource Planning
LIMS
OPC
RESTful
Data Visualization
Decision-making
Dashboard
Management
Reporting
Technical Support
Manufacturing Execution System
Onboarding
Manufacturing Operations
Documentation
GDP
Data Integrity
Computer Science
Pharmaceutics
Biotechnology
GxP
GAMP
Computerized System Validation
MES
SQL
Python
C#
Manufacturing
System Integration
Conflict Resolution
Problem Solving
Analytical Skill
Effective Communication
Collaboration
Regulatory Compliance

Summary

ssist in the design and configuration of Tempo MES solutions, including electronic batch records (eBRs), under the guidance of senior engineers.
Contribute to the development of modular, scalable, and reusable MES recipe templates based on ISA 88/95 standards.
Perform impact assessments for recipe modifications and system updates, ensuring adherence to GxP requirements.
Collaborate with cross-functional teams to gather user requirements and define functional specifications for MES functionalities.
ssist in recipe design and authoring electronic batch records (eBR) to develop modular, scalable and reusable MES recipe and equipment workflow templates following ISA 88/95 standards.
Perform root cause analysis and resolve MES issues related to system configuration, recipe design, or integration failures.
Support efforts to integrate MES with other enterprise systems, such as ERP, LIMS, and automation platforms, using industry-standard protocols like OPC or RESTful APIs.
ssist in the development of data visualization tools and reporting dashboards to support operational decision-making.
Possess technical knowledge in DCS, automation, and systems integration, including the design and management of data dashboards, label management systems, and reporting tools.
Provide day-to-day technical support for MES system users, assisting in troubleshooting and resolving recipe or system-related issues.
Participate in technical transfer activities to ensure smooth onboarding of new products and processes into manufacturing.
Support off-hours manufacturing operations as needed to address critical MES-related issues.
Ensure compliance with Good Documentation Practices (GDP), GxP regulations, Data Integrity guidelines and company policies during all MES-related activities.
Participate in validation activities to support the implementation and ongoing maintenance of MES systems.

Required Qualifications:

Bachelor's degree in Engineering, Computer Science, or a related technical field.
2-4 years of experience with MES systems, preferably some in Drug Product manufacturing in pharmaceutical or biotechnology environments.
Basic understanding of GxP regulations, GAMP guidelines, and Computer System Validation (CSV).
Exposure to MES platforms such as Tempo, Syncade, or equivalent systems is preferred.
Familiarity with basic programming concepts or languages like SQL, Python, or C#.
General knowledge of manufacturing processes, automation systems, and systems integration principles.
Strong problem-solving and analytical skills with a willingness to learn and adapt quickly.
Effective communication and collaboration abilities to work in cross-functional teams.
Commitment to maintaining compliance with regulatory and internal standards

Dice Id: 91116760
Position Id: 1fd832d1951c539f3d13b9c1403ee661
Posted 2 days ago

Fitment

Dice Job Match Score™

🔢 Crunching numbers...

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Similar Jobs

MES Engineer

Massachusetts

•

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Lead SAP MES Consultant

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