Specialist, Manufacturing Automation

EyeBio; West Point (PA); Hybrid; USD 87,000 - 137,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Comprehensive benefits package

Job summary

Merck & Co., Inc. is seeking a Manufacturing Automation Specialist for the West Point site. You will support connected instruments, qualify and test integrations with MES, and help ensure compliant production of vaccines.

The role requires knowledge of DeltaV DCS, AB PLC, SCADA/HMI, and regulatory CSV/GxP. Hybrid work flow is available, with strong collaboration across manufacturing, quality, and engineering teams.

Qualifications

• Bachelor’s degree in Engineering, Computer Science, Electrical, Chemical, Mechanical, or related field with 2 years in automation/validation.
• Associate’s degree plus 3 years in automation/validation.
• High school diploma plus 6 years in automation/validation.

Responsibilities

• Design, test, and close out change controls for corrective actions and improvements.
• Interface with manufacturing, quality, and engineering groups to resolve technical issues.
• Stay current with automation trends and recommend new technologies.
• Lead investigations of incidents to prevent recurrence and implement corrective actions.
• Ensure compliance with cGMP, CSV, and SDLC in daily activities.
• Collaborate across teams to support manufacturing automation.

Skills

Communication

Interpersonal skills

Team collaboration

Change management

Problem solving

Analytical thinking

Operational excellence

Documentation

Auditing

Regulatory understanding

Education

Bachelor's degree in engineering or related field

Associate's degree in related field

High school diploma + extensive automation experience

Tools

DeltaV DCS

Allen-Bradley PLC

SCADA

HMI

ASi/Field/Profibus

Networking/IT administration

Power BI

Job description

Job Description

Our Digital Manufacturing Operations Team, supporting our West Point site, is seeking a Manufacturing Automation Specialist. This role will provide system support for connected instruments such as pH/conductivity meters and spectrophotometers, including qualification and integration testing for manufacturing instrument connections to MES.

Use your expertise to help enable our manufacturing division in the reliable and compliant supply of quality vaccine products to customers and patients around the globe, while maintaining system compliance with SDLC, GMP, safety, and environmental regulations. The role actively supports and promotes a diverse and inclusive culture through significant interaction with manufacturing, quality, and engineering groups.

General Responsibilities

• Work independently and as a team member with Integrity, Precision, Accomplishment, Motivational Ambition, Respect, and Inclusion.

• Comply with global policies, procedures, and guidelines; regulatory requirements; and current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions.

• Design, implement, test, and close out change controls for corrective actions and continuous improvement initiatives.

• Build relationships with functional counterparts and business stakeholders to proactively identify and resolve technical issues.

• Lead or participate in investigations of incidents and problems to prevent recurrence, including the development and implementation of corrective actions.

• Stay current with the latest automation technologies and trends and make recommendations for adoption.

Skill Requirements

• Strong communication and interpersonal skills to interface effectively with colleagues at all levels in a team environment.

Preferred Skills

• Experience in GMP manufacturing within the pharmaceutical or biotechnology industry.

• Familiarity with computer system validation and regulatory GxP requirements.

• Aseptic processing and/or sterile manufacturing experience.

• Technical and operational expertise in DeltaV DCS, Allen-Bradley PLC, SCADA, HMI, ASi/Field/Profibus, or related technologies.

• Experience with networking, virtual machines, database management, and general IT administration.

• Experience with data analytics tools such as Power BI.

Education Requirements

• Bachelor’s degree in Engineering, Computer Science, Electrical, Chemical, Mechanical, or a related field, plus 2 years of experience in process automation, instrument validation, or a related area.

• Associate’s degree in Engineering, Science, Information Technology, or a related field, plus 3 years of experience in process automation, instrument validation, or a related area.

• High school diploma, plus 6 years of experience in process automation, instrument validation, or a related area.

Required Skills:

• Audit Management
• Automation
• Automation Systems
• Automation Technology
• Biopharmaceutical Manufacturing
• Biotechnology Manufacturing
• Business Process Improvements
• Change Control Processes
• Change Controls
• Computer System Validation (CSV)
• Corrective Action Management
• Data Management
• Environmental Controls
• Equipment Troubleshooting
• Global Coordination
• Manufacturing Automation
• Pharmaceutical Manufacturing
• Policy Compliance
• Problem Management
• Quality Management
• Real-Time Programming
• Software Development Life Cycle (SDLC)
• System Validation
• Team Communication
• Working Independently

Preferred Skills:

US and Puerto Rico Residents Only:

Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities.

As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:

EEOC Know Your Rights

EEOC GINA Supplement

We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively.

Learn more about your rights, including under California, Colorado and other US State Acts

The salary range for this role is

$87,300.00 - $137,400.00

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee’s position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits

You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting.

San Francisco Residents Only:

We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance

Los Angeles Residents Only:

We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles’ Fair Chance Initiative for Hiring Ordinance

Search Firm Representatives Please Read Carefully
Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.

Employee Status:

Regular

Relocation:

No relocation

VISA Sponsorship:

No

Travel Requirements:

No Travel Required

Flexible Work Arrangements:

Hybrid

Shift:

1st - Day

Valid Driving License:

No

Hazardous Material(s):

n/a

Job Posting End Date:

09/8/2026

A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.