Associate Specialist, Manufacturing Automation

Merck; West Point (PA); On-site; USD 90,000 - 130,000; Full time

Job summary

Merck, at its West Point site, seeks a Process Automation Engineer Associate to support automation systems for vaccine manufacturing. The role involves problem resolution, data collection, and cross-functional collaboration with Manufacturing, Quality, and Engineering teams to ensure compliant, reliable production.

The position emphasizes change controls, continuous improvement, and staying current with automation technologies.

Qualifications

• BS in Engineering, Computer Science or related field, or HS Diploma with 2 years GMP Manufacturing/Automation experience.
• Strong verbal and written communication skills with interpersonal abilities.
• Ability to work effectively in a team environment while managing individual responsibilities.

Responsibilities

• Work independently and as a team member while upholding Integrity, Precision and Respect.
• Comply with cGMP, regulatory requirements and SDLC in daily activities.
• Provide automation system support to manufacture quality vaccine products.
• Design, implement, test, and close change controls related to automation actions.
• Lead investigations of automation incidents and implement corrective actions.
• Stay aware of emerging automation technologies and advise on adoption.

Skills

Communication skills

Teamwork

Education

BS in Engineering/CS or related field

High School Diploma + 2 years GMP experience

Job description

Position Overview

Our Digital Manufacturing Operations Team supporting our vibrant West Point site is seeking a Process Automation Engineer Associate to join our 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.

Job Description

Position Overview

Our Digital Manufacturing Operations Team supporting our vibrant West Point site is seeking a Process Automation Engineer Associate to join our 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 and participate in a collaborative and respectful work environment, including significant interaction with Manufacturing, Quality, and Engineering groups. Supports a broad spectrum of automated systems within GMP Manufacturing Operations.

Key Functions

• Work independently and as a team member while demonstrating Integrity, Precision, Accomplishment, Motivational Ambition, and Respect.
• Comply with Global Policies, Procedures, Guidelines, regulatory requirements, and 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 in the manufacture of quality vaccine products and support site priorities.
• Support all automation system components associated with manufacturing processes, including shop floor support of manufacturing activities.
• Design, implement, test, and close change controls related to automation 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 automation incidents and issues to prevent recurrence, including development and implementation of corrective actions.
• Maintain awareness of emerging automation technologies and industry trends and provide recommendations for adoption where appropriate.
• Provide off-shift, weekend, evening, remote, or on-site automation support for 24/7 manufacturing operations as required.

Education

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

Experience, Skills & Knowledge

• Strong verbal and written communication skills and interpersonal abilities, with the capability to effectively interact with colleagues at all organizational levels and external partners.
• Ability to work effectively in a team environment while managing individual responsibilities.

Preferred

• Experience in the pharmaceutical or biotechnology industry.
• Knowledge of and/or experience with process control systems.
• Experience supporting aseptic processing and/or sterile manufacturing operations.
• Technical and operational experience with computer systems, automation technologies, and programming.

Aseptic Processing, Aseptic Processing, Audit Management, Automation, Biotechnology, Biotechnology Industry, Business Process Improvements, Change Control Processes, Change Controls, Computer Programming, Computer Science, Corrective Action Management, Data Management, Good Manufacturing Practices (GMP), Interpersonal Communication, Manufacturing, Pharmaceutics, Problem Management, Process Control, Quality Management, Real-Time Programming, Software Development Life Cycle (SDLC), Systems Programming, Vaccine Administration, Vaccine Development {+ 1 more}

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.

Requirements

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:

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