Specialist, Automation Engineering

MSD

Confirmed live yesterday High trust
Closes in 6 days

Quick summary

Work type
On-site
Location
Rahway, NJ
Salary
$87,300–$137,400 / yr
Employment
Full-time
Posted
8 days ago
Freshness
Confirmed live yesterday
Closes
Oct 9, 2026 (soon)

Market check

Salary context

Below market

How this pay compares to similar roles

Similar $158k
This role $112k
$75k most similar roles pay here $199k

This role pays less than 89% of similar roles. Most pay $129,887–$186,612 — the shaded band above. At the midpoint, this role pays about $112k versus about $158k for comparable roles.

Based on 240 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 8 open roles on FindRole.

Listed pay typically runs $117,000–$184,200 across 7 roles with salary data.

Most-posted roles

View all roles at MSD

At a glance

TL;DR · Specialist, Automation Engineering

Specialist, Automation Engineering - 2nd Shift (Onsite) provides end-to-end automation engineering support for the FLEx Center, focusing on sterile clinical manufacturing within Pharmaceutical Sciences and Clinical Supply. The role involves maintaining validated systems in a compliant state, performing root cause analysis, and managing the automation lifecycle including commissioning, qualification, and change control. You will build and sustain platform solutions, manage data integrity, and oversee capital projects involving OT/IT architecture. Key technical requirements include proficiency with Allen-Bradley or Siemens PLCs, SCADA systems like iFix, WinCC OA, or Ignition, and industrial networking protocols such as Profibus and Profinet. Candidates should be skilled in Ladder Logic and Python scripting while navigating S88 batch standards. This role solves critical manufacturing challenges by ensuring reliable operation of formulation, filling, and lyophilization processes for sterile small molecules, biologics, vaccines, and antibody-drug conjugates.

What you'll do

  • Maintain automation systems in a validated, compliant state per cGMP, safety, and data integrity standards.
  • Provide on-floor troubleshooting and root cause analysis for sterile manufacturing processes including formulation and filling.
  • Manage the full automation lifecycle including change control, risk assessments, and regulatory filing support.
  • Lead the installation, integration, and qualification of new automated equipment and systems.
  • Represent automation interests in capital projects by integrating OT/IT architecture and cybersecurity requirements.
  • Develop data reporting and visualization solutions using historian and SCADA sources to monitor asset health.
  • Coordinate with vendors and contract engineers to manage project deliverables and technical execution.
  • Perform off-shift or weekend work as needed to support manufacturing operations and system reliability.

What we're looking for

  • Bachelor’s degree in Engineering, Science, Information Technology, or a related field.
  • Minimum of 2 years of experience in process automation or equivalent.
  • Strong knowledge of cGMP, Quality Systems, Safety, data integrity, and validation principles for automation and computer systems.
  • Hands-on experience maintaining validated automation systems, executing change control, investigations/CAPA, and system administration within GMP operations.
  • Proficiency with PLC/SCADA and industrial networking fundamentals to troubleshoot across controls, instrumentation, electrical, and software layers.
  • Strong technical writing skills and ability to lead cross-functional teams without authority.
  • Experience in biologics, vaccine, or bulk sterile manufacturing facilities (preferred).
  • Familiarity with Allen-Bradley/Siemens PLCs, SCADA systems, and S88 batch standards (preferred).

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