Manufacturing Execution System (MES) Site Lead

MSD

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
De Soto, KS
Salary
$117,000–$184,200 / yr
Posted
3 days ago
Freshness
Confirmed live yesterday
Closes
Sep 30, 2026

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $182k
This role $151k
$104k most similar roles pay here $239k

This role pays less than 75% of similar roles. Most pay $151,147–$213,250 — the shaded band above. At the midpoint, this role pays about $151k versus about $182k for comparable roles.

Based on 239 similar postings.

Employer

About MSD

MSD (Merck Sharp & Dohme) is the international name for Merck & Co., a major U.S.-based pharmaceutical company.

MSD currently has 25 open roles on FindRole.

Listed pay typically runs $117,000–$184,200 across 25 roles with salary data.

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View all roles at MSD

At a glance

TL;DR · Manufacturing Execution System (MES) Site Lead

The Manufacturing Execution System (MES) Site Lead joins the Digital Records Design Hub at the DeSoto site to manage and support MES components within a biopharmaceutical manufacturing environment. This role involves providing on-floor support for manufacturing activities, managing vendor performance, and ensuring automation systems remain in a validated state. The individual will develop and implement methodologies for MES Systems Version 3.4 and future versions while maintaining recipes, performing update processes, and drafting SOPs in compliance with SDLC requirements. Key responsibilities include resolving technical issues through the Tier process and collaborating across functions to ensure reliable performance. Required skills include proficiency in Microsoft Office, data analysis, and knowledge of USDA, European, and International Codes. The role addresses the critical need for maintaining validated systems and ensuring regulatory compliance within a complex pharmaceutical production landscape.

What you'll do

  • Provide on-floor support for manufacturing activities and resolve technical issues before they impact business priorities.
  • Develop and implement optimal methodologies for managing MES systems in compliance with quality regulations and industry norms.
  • Manage vendor performance, contracts, and investigations to find resolutions to MES problems.
  • Support, maintain, and develop MES recipes and capabilities to ensure reliable and sustainable performance.
  • Perform MES administration and maintenance to ensure automation systems remain in a validated state.
  • Execute Update/Change Processes ensuring all actions are completed on time according to quality standards.
  • Develop and update Standard Operating Procedures (SOPs) and conduct training for the MES system.
  • Ensure all technical documentation complies with System Development Life Cycle (SDLC) requirements.

What we're looking for

  • Bachelor of Science degree in a technical field (engineering or science) or equivalent.
  • Minimum of five years experience in Manufacturing Execution Systems (MES).
  • Knowledge of regulatory requirements for USDA, European, and International Codes, Standards, and Practices.
  • Proficiency in Microsoft Office and job-related computer applications.
  • Strong problem-solving, troubleshooting, and data analysis skills.
  • Experience in the application of Lean Six Sigma Methodology (preferred).
  • Pharmaceutical and Biotechnology manufacturing process experience (preferred).
  • Extensive knowledge of equipment and process validation (preferred).

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