Merck KGaA Posted August 15, 2026

Automation Engineer

Kankakee, Illinois, United States FULL_TIME
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Merck KGaA is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Work Your Magic with us!  Start your next chapter and join MilliporeSigma.

Ready to explore, break barriers, and discover more? We know you’ve got big plans – so do we! Our colleagues across the globe love innovating with science and technology to enrich people’s lives with our solutions in Healthcare, Life Science, and Electronics. Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet. That's why we are always looking for curious minds that see themselves imagining the unimaginable with us.

This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the US.

Your Role:

As the Automation/ Operational Technology Engineer, you are responsible for the design, implementation, maintenance, and continuous improvement of automated control systems across our manufacturing operations. Serving as the subject matter expert (SME) for all automation and control activities, you will collaborate closely with production, maintenance, process engineering, and safety teams to ensure the reliable, efficient, and safe operation of all automated equipment.

This is an on-site, hands-on engineering role that requires both deep technical expertise and strong collaborative skills. The position is based out of Kankakee, Illinois and will support our production site in Urbana, Illinois as needed (twice per month). Travel may be required up to 20% of the time.

1. Control System Design & Implementation

Design, develop, commission, and test PLC, DCS, HMI, and SCADA systems for new and existing production equipment.

Create and maintain detailed system documentation, including electrical schematics, network architecture diagrams, I/O lists, and functional design specifications.

Collaborate with equipment vendors and system integrators to ensure designs meet site standards, project requirements, and corporate data integrity policies.

Lead Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) for new installations.

2. Production Support & Troubleshooting

Provide first-line technical support for control system faults, alarms, and unexpected production downtime events.

Diagnose and resolve complex electrical and controls-related issues quickly to minimize operational disruption.

Provide daily oversight of site automation to ensure reliable operations and establish clear escalation paths for critical issues.

Analyze alarm data, downtime trends, and system performance metrics to identify and eliminate recurring root-cause issues.

Develop and maintain practical fault-finding guides and troubleshooting documentation for the maintenance team.

3. Continuous Improvement & Capital Projects

Identify and champion opportunities to improve Overall Equipment Effectiveness (OEE) through control system enhancements.

Lead, execute, and support capital improvement projects from initial scope definition through commissioning and final handover.

Implement alarm management strategies (aligned with ISA-18.2 standards) to reduce nuisance alarms and improve operator effectiveness.

Drive the standardization of control system hardware, software platforms, and programming practices across the site.

Evaluate and introduce emerging technologies, including advanced process control, data analytics, and IIoT integration.

4. Cybersecurity & Network Management

Maintain the integrity and security of the Industrial Control System (ICS) network.

Implement and enforce cybersecurity best practices in line with IEC 62443 standards and company policy.

Manage control system patching, regular backups, and disaster recovery procedures.

Partner with the IT department to ensure appropriate, secure segmentation between OT (Operational Technology) and IT networks.

Control, monitor, and audit remote access to production control systems.

5. Safety, Compliance & Change Management

Ensure all control system designs and modifications comply with functional safety standards (including IEC 61511 and IEC 62061).

Participate in HAZOP, Risk Assessments, and System Integrity Level (SIL) studies; implement required Safety Instrumented Functions (SIFs).

Maintain and test Safety Instrumented Systems (SIS) in accordance with the site’s safety lifecycle plan.

Manage all control systems changes strictly through the site’s Management of Change (MOC) process and maintain version control for all program files.

Update Standard Operating Procedures (SOPs), as-built documentation, and training records following any system modifications.

Ensure all work complies with site electrical safety rules, lockout/tagout (LOTO) procedures, and work permit systems.

Who You Are:

Minimum Qualifications:

Bachelor’s Degree in Engineering (Electrical, Control Systems, Mechatronics, etc.)

2+ years of hands-on experience in an industrial manufacturing or process environment

2+ years experience programming and commissioning Allen-Bradley (Rockwell Automation) and/or Siemens PLCs

1+ years experience working with HMI/SCADA platforms such as FactoryTalk View, Ignition, WinCC, or equivalent

1+ years experience working with industrial networking including Ethernet/IP, Profinet, Modbus TCP, and DeviceNet

Preferred Qualifications:

Ability to troubleshoot complex automated systems under pressure

Strong understanding of electrical control panel design and the ability to read and interpret electrical drawings

Experience with DCS platforms such as Emerson DeltaV, Honeywell Experion, or ABB 800xA

Experience with building automation systems i.e. METESYS, Automated Logic

Familiarity with functional safety lifecycle processes and IEC 61511 / IEC 62061

Knowledge of ISA-18.2 alarm management methodology

Experience with IIoT platforms, data historians (OSIsoft PI, Wonderware), or MES integration

Exposure to Lean Manufacturing or Six Sigma methodologies

TÜV Functional Safety Engineer certification is an advantage

Experience working in a regulated manufacturing environment such as food and beverage, pharmaceutical, or chemical processing

Pay Range for this position - $78,300 - $119,000

The offer range represents the anticipated low and high end of the base pay compensation for this position. The actual compensation offered will be determined by factors such as location, level of experience, education, skills, and other job-related factors. Position may be eligible for sales or performance-based bonuses. Benefits offered by the Company include health insurance, paid time off (PTO), retirement contributions, and other perquisites. For more information click here .

RSREMD

What we offer: We are curious minds that come from a broad range of backgrounds, perspectives, and life experiences. We believe that this variety drives excellence and innovation, strengthening our ability to lead in science and technology. We are committed to creating access and opportunities for all to develop and grow at your own pace. Join us in building a culture of inclusion and belonging that impacts millions and empowers everyone to work their magic and champion human progress!

Apply now and become a part of a team that is dedicated to Sparking Discovery and Elevating Humanity!

Job details

Seniority
Not listed
Function
Manufacturing & CMC
Therapeutic area
Not listed
Location
Kankakee, Illinois, United States
Employment type
FULL_TIME

How this role compares

Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.

We currently track 2556 comparable Manufacturing & CMC roles across 173 biopharma companies.

2556Comparable roles tracked
2343Currently active
173Companies hiring similar roles
56Countries represented

Salary context

662 of 2556 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject $78,300/yr – $119,000/yr
Lowest disclosed · Associate Director, Digital Scientific Workflows · Merck $0/hr – $0/hr (≈ $0–$0/yr)
Highest disclosed · VP, CMC Development Technical Strategy · ModernaTX, Inc. $272,200/yr – $490,100/yr
Peer group range $0 – $381,150 (median $122,400)

Where these roles are based

Top locations among the 2556 comparable roles

United States1232
India167
Germany134
France95
Ireland91
Netherlands77

+ 50 more countries

Seniority mix

1172 of 2556 peers have a known seniority level

Senior323
Manager265
Associate154
Intern/Fellow/Postdoc147
Principal88
Director79
Associate Director75
Senior Director34
Executive/VP7

Therapeutic area mix

12 of 2556 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease7
Rare Disease2
Oncology2
Dermatology & Aesthetics1

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How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
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Function Therapeutic area Seniority Country
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Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.