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Mes Manager Jobs in Delaware (NOW HIRING)

Pivotal Solutions

Accounting Manager

Newark, DE · On-site

Experience utilizing ERP/MES. * Experience in a manufacturing environment required. * Sound knowledge of accounting principles, standards, and regulations. * Superior data management and data ...

NextGenEnergyJobs

Smart Factory Manager

Newark, DE · On-site

$150 - $200/hr

Manage the smart factory's technology stack, including the Operational Technology (OT) and IT infrastructure. This involves managing systems like Manufacturing Execution Systems (MES), Supervisory ...

TAI

Manufacturing Manager

New Castle, DE · On-site

$100K - $140K/yr

Proficiency with Microsoft Office and enterprise manufacturing systems (SAP or similar ERP/MES platforms). * Experience managing supervisors or shift leads. Preferred Qualifications: * Experience in ...

TAI

Manufacturing Manager

New Castle, DE · On-site

$100K - $140K/yr

Proficiency with Microsoft Office and enterprise manufacturing systems (SAP or similar ERP/MES platforms). * Experience managing supervisors or shift leads. Preferred Qualifications: * Experience in ...

Bloom Energy

Smart Factory Manager

Newark, DE

Manage the smart factory's technology stack, including the Operational Technology (OT) and IT infrastructure. This involves managing systems like Manufacturing Execution Systems (MES), Supervisory ...

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Mes Manager information

See Delaware salary details

$28.5K

$62.7K

$113.6K

How much do mes manager jobs pay per year?

As of Sep 8, 2026, the average yearly pay for mes manager in Delaware is $62,715.00, according to ZipRecruiter salary data. Most workers in this role earn between $45,000.00 and $69,100.00 per year, depending on experience, location, and employer.

What is a MES manager?

A MES Manager oversees the implementation, operation, and maintenance of Manufacturing Execution Systems (MES) within a manufacturing organization. They are responsible for ensuring the MES effectively connects, monitors, and controls complex manufacturing processes on the shop floor. The role involves coordinating between IT and production teams, optimizing system performance, managing upgrades, and ensuring data integrity. MES Managers play a key role in streamlining production, improving efficiency, and supporting digital transformation in manufacturing environments.

What are the key skills and qualifications needed to thrive as a MES manager?

To thrive as a MES Manager, you need expertise in manufacturing processes, IT systems integration, and project management, usually supported by a degree in engineering, computer science, or a related field. Familiarity with MES platforms (such as Siemens SIMATIC IT, Rockwell FactoryTalk, or Wonderware), database management, and relevant certifications like PMP or Six Sigma are typically required. Strong analytical thinking, leadership, and effective communication skills help you collaborate across departments and drive system adoption. These skills are crucial for optimizing production efficiency, ensuring data accuracy, and successfully leading MES implementation or improvement projects.

How does a MES manager typically collaborate with other departments to ensure smooth production workflows?

An MES Manager works closely with production, IT, quality assurance, and engineering teams to integrate manufacturing execution systems with existing processes. They facilitate communication between departments by translating business needs into technical requirements and ensuring MES solutions support operational goals. Regular cross-functional meetings, process mapping, and continuous feedback loops are common practices to identify bottlenecks and implement improvements. This collaborative approach helps maintain production efficiency and ensures that system changes align with overall business objectives.

What is the difference between Mes Manager vs Manufacturing Supervisor?

AspectMes ManagerManufacturing Supervisor
CredentialsTypically requires a degree in engineering, manufacturing, or related field; certifications in MES systems are commonHigh school diploma or associate degree; experience in manufacturing often preferred
Work EnvironmentOffice and production floor; focuses on system management and process optimizationPrimarily on the production floor overseeing daily operations
Employer & Industry UsageManufacturing plants utilizing MES systems; industries like automotive, electronics, and pharmaceuticalsManufacturing facilities across various industries; more hands-on operational role

The Mes Manager primarily manages Manufacturing Execution Systems, requiring technical knowledge and system management skills, while the Manufacturing Supervisor oversees daily production activities on the shop floor. Both roles are essential in manufacturing but differ in focus, credentials, and work environment.

What job categories do people searching Mes Manager jobs in Delaware look for?

The top searched job categories for Mes Manager jobs in Delaware are:

What cities in Delaware are hiring for Mes Manager jobs?

Cities in Delaware with the most Mes Manager job openings:

Mes Manager jobs near you
Infographic showing various Mes Manager job openings in Delaware as of August 2026, with employment types broken down into 86% Full Time, 13% Part Time, and 1% Contract. Highlights an 79% Physical, 3% Hybrid, and 18% Remote job distribution, with an average salary of $62,715 per year, or $30.2 per hour.

Digitalization Lead, MES/ SAP

WuXi AppTec

Middletown, DE • On-site

Other

Posted 25 days ago

Job description

Overview
We are seeking a high-energy, results-driven Digitalization Lead to spearhead the digital transformation roadmap at our Middletown manufacturing site. In this role, you will actively drive the end-to-end implementation, integration, and optimization of core enterprise and shop-floor systems, including ERP, LIMS, and MES. Serving as a critical bridge between local operations and global teams, you will deploy technical solutions that maximize operational efficiency while strictly maintaining FDA compliance, GMP validation, and data integrity standards. The ideal candidate brings a heavy blend of IT technical expertise and rigorous project management execution, backed by professional bilingual fluency in both English and Chinese to seamlessly coordinate across international boundaries.
Responsibilities
  • Develop site digitalization roadmap, focusing on integration of ERP, LIMS, MES, etc.
  • Lead & manage end-to-end ERP (e.g., SAP/Oracle) implementation, upgrade, and maintenance, ensuring pharmaceutical compliance.
  • Lead & manage end-to-end manufacturing execution and operation management system (e.g., MES/WMS) implementation, upgrade, and maintenance, ensuring pharmaceutical compliance.
  • Collaborate across IT, Manufacturing, Quality, and Supply Chain to organize resources for project management & execution.
  • Ensure digital solutions comply with FDA/EMA data integrity principles (ALCOA+) and computer system validation (CSV) under GxP/GMP standards.
  • Manage multiple projects with accountability for budget, timeline, risk mitigation, and milestone delivery.
  • Establish project governance structures, reporting progress regularly to site leadership or steering committees.

Qualifications
  • Bachelor's/Master's in Computer Science, IT, or related field.
  • 5+ years of digital project management experience specifically within a pharmaceutical manufacturing, biotech, or CDMO environment with deep knowledge of GMP/GxP.
  • 3+ years of hands-on experience in large-scale ERP system implementations (e.g., SAP, Oracle), with a strong grasp of manufacturing and supply chain modules.
  • Deep understanding of pharmaceutical regulatory frameworks, including Current Good Manufacturing Practices (cGMP), 21 CFR Part 11
  • Proven organizational skills in managing cross-functional teams and vendors.
  • Strong project management capability; PMP/Prince2 certification preferred.
  • Native or professional fluency in English is required; Mandarin is a plus, to effectively coordinate with global teams and stakeholders.
  • Experience in multinational pharma or CDMO manufacturing sites preferred.
  • Knowledge of drug discovery and pharmaceutical process development processes preferred.

An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability
This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management.

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