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Spclst , Manufacturing Automation
full-timeUnited States$85k - $134k

Summary

Location

United States

Salary

$85k - $134k

Type

full-time

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About this role

Job Description

Our Digital Manufacturing Operations Team supporting our vibrant West Point site is seeking a Process Automation Engineer Specialist to join their Team. This role will provide automation system support and expertise to enable our manufacturing division in the reliable and compliant supply of quality vaccine products to customers and patients across the globe.

Responsible for problem resolution, implementation of process control, data collection techniques, and troubleshooting in compliance with SDLC, GMP, safety, and environmental regulations.  Actively support, participate and embrace a diverse and inclusive culture including significant interaction with manufacturing, quality and engineering groups.  Supports a broad spectrum of automated systems within GMP Manufacturing Operations. 

General responsibilities include:

  • Work Independently and as a Team member with Integrity | Precision | Accomplishment | Motivational Ambition | Respect | Inclusion

  • Comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions.

  • Provide automation system support and expertise to assist the manufacture of quality vaccine products to meet site priorities.

  • Responsible and accountable for supporting all automation system components of the processes including on the shop floor support of manufacturing activities

  • Responsible for designing, implementing, testing, and closing-out change controls for automation related corrective actions and continuous improvement initiatives.

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

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

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

  • Provide off-site weekend/evening automation phone or on-site support for our 24/7 manufacturing operations.

Skill Requirements:

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

Preferred Skills:

  • Experience in GMP Manufacturing - pharmaceutical/ biotechnology industry.

  • Familiarly with Computer system validation and regulatory GXP requirements.

  • Aseptic processing/sterile manufacturing experience.  

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

  • Networking, Virtual Machines, Database management and other general IT administration.

  • Experience with data analytics tools (e.g. Spotfire, PowerBI)

Education Requirements:

  • BS in Engineering, Computer Science or related field with 2 years of experience (GMP Manufacturing and/or Manufacturing Automation)

Or

  • High School Diploma and with 4 years of experience (GMP Manufacturing and/or Manufacturing Automation)

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Required Skills:

cGMP Regulations, Communication, Data Collection Methods, Data Management, Digital Manufacturing, Environmental Regulations, GMP Compliance, Good Manufacturing Practices (GMP), Problem Management, Process Control, Real-Time Programming, Software Development Life Cycle (SDLC), Technical Issues, Test Automation, TIBCO Spotfire

Preferred Skills:

Current Employees apply HERE

Current Contingent Workers apply HERE

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. Please click here if you need an accommodation during the application or hiring process.

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

U.S. Hybrid Work Model

Effective September 5, 2023, employees in office-based positions in the U.S. will be working a Hybrid work consisting of three total days on-site per week, Monday - Thursday, although the specific days may vary by site or organization, with Friday designated as a remote-working day, unless business critical tasks require an on-site presence.This Hybrid work model does not apply to, and daily in-person attendance is required for, field-based positions; facility-based, manufacturing-based, or research-based positions where the work to be performed is located at a Company site; positions covered by a collective-bargaining agreement (unless the agreement provides for hybrid work); or any other position for which the Company has determined the job requirements cannot be reasonably met working remotely. Please note, this Hybrid work model guidance also does not apply to roles that have been designated as “remote”.

The salary range for this role is

$85,600.00 - $134,800.00

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:

Domestic

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:

01/26/2026

*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.

Other facts

Tech stack
Communication,Data Collection Methods,Data Management,Digital Manufacturing,Environmental Regulations,GMP Compliance,Good Manufacturing Practices,Problem Management,Process Control,Real-Time Programming,Software Development Life Cycle,Technical Issues,Test Automation,TIBCO Spotfire

About MSD

At MSD, known as Merck & Co., Inc., Rahway, NJ, USA in the United States and Canada, we are unified around our purpose: We use the power of leading-edge science to save and improve lives around the world. For more than 130 years, we have brought hope to humanity through the development of important medicines and vaccines. We aspire to be the premier research-intensive biopharmaceutical company in the world – and today, we are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals. We foster a diverse and inclusive global workforce and operate responsibly every day to enable a safe, sustainable and healthy future for all people and communities. For more information, visit www.msd.com and connect with us on Facebook, Instagram, Twitter, and YouTube.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing

What you'll do

  • The role involves providing automation system support and expertise to ensure the reliable supply of quality vaccine products. Responsibilities include problem resolution, implementation of process control, and troubleshooting in compliance with regulations.

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Frequently Asked Questions

What does MSD pay for a Spclst , Manufacturing Automation?

MSD offers a competitive compensation package for the Spclst , Manufacturing Automation role. The salary range is USD 86k - 135k per year. Apply through Clera to learn more about the full compensation details.

What does a Spclst , Manufacturing Automation do at MSD?

As a Spclst , Manufacturing Automation at MSD, you will: the role involves providing automation system support and expertise to ensure the reliable supply of quality vaccine products. Responsibilities include problem resolution, implementation of process control, and troubleshooting in compliance with regulations..

Why join MSD as a Spclst , Manufacturing Automation?

MSD is a leading Pharmaceutical Manufacturing company. The Spclst , Manufacturing Automation role offers competitive compensation.

Is the Spclst , Manufacturing Automation position at MSD remote?

The Spclst , Manufacturing Automation position at MSD is based in United States, United States. Contact the company through Clera for specific work arrangement details.

How do I apply for the Spclst , Manufacturing Automation position at MSD?

You can apply for the Spclst , Manufacturing Automation position at MSD directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about MSD on their website.