Organizes, plans, directs, and supports Production, Project, Validation and Maintenance activities in order that equipment, systems, and facilities are safe, efficiently utilized, reliable and meet cGMP, regulatory or production requirements.
Main Responsibilities
Assists in the Mechanical, Electrical, and Instrumentation (MEI) engineering providing troubleshooting support with the goal of increasing operational efficiencies and minimizing maintenance expenses
Assists in the support of unit operations and/or running the utility plant equipment
Supports the corrective and preventive maintenance for MEI systems
Completes compliance-related requirements
Completes jobs assigned by Supervisor pertaining to installation, modification, fabrication, testing, servicing, and repairs of equipment, with adherence to site change control procedures or minor projects requirements
Assists in performing testing, commissioning, and qualification (IQ, OQ) activities
Assists in maintenance related project schedule, costs and quality utilising proper controls. This could be a sub-component of a larger project
Assists in the evaluation of design solutions and provide feedback for the project team
Assists in the scoping, development, execution and documentation of upgrade projects
Assists in process control systems projects
As part of a project team or Individually responsible for the scoping, development, execution, and documentation of small projects within the allotted timeline, budget, design requirements, and established quality standards.
Identifies, executes, and makes improvement on routine work activities
Assists in the assessment or improvement studies to enhance equipment or system efficiency, reduce energy costs or usage and other cost saving avoidance projects
Completes job assignments by Supervisor pertaining to equipment, system, documentation, or housekeeping
Assists in monitoring the performance and implementing Safety, Health, and Environment (SHE) improvement initiatives (i.e., audits, training, etc)
Provides technical support to process control systems projects. Works under guidance to ensure compliance with corporate, industry, regulatory and computer validation standards
Assists in the selection, and installation of automation systems
Assists with software development, configuration, programming, and documentation for various automation platforms
Works under guidance of Senior Engineer to perform system security back-up & recovery, managing electronic records and performance monitoring duties
Helps with developing technical procedures and related change management documentation
Participates in SHE, Business Compliance, cGMP, and all other compliance-related matters, where applicable
Supervises and oversees Third Party Contractors, where applicable
Completes any other tasks as and when assigned by Supervisors
Technical Competencies
Develops an awareness of Engineering and Compliance standards through assigned tasks and training
Develops an awareness of the practical application of theoretical engineering knowledge
Develops an understanding of planning related to assigned engineering role
Assists in planning activities related to assigned engineering role
Assists in the providing of data to support risk-based decisions
cGMP Standards
Understands and follows appropriate training in cGMP principles
Shows basic knowledge of the principles and importance of cGMP regulations and Worldwide Quality Standards related to the execution of assigned work
Provides solutions to routine and a wide variety of problems ranging from simple to moderate in scope and complexity
Able to assess the situation and understand when to escalate to a higher level
Develops competency in root cause analysis
Qualification
Bachelor of Engineering (Mechanical/ Mechatronics / Electrical or Instrumentation & Control Engineering) or equivalent
Experience:
Work experience required
; Previous experience in pharmaceutical (preferred), chemical or semiconductor industry.
Other Competencies and Personal Attributes
Develops skills associated with providing logically structured, grammatically correct report writing
Provides accurate routine verbal and written communications
Provides and presents information in a clear and unambiguous manner
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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:
Intern/Co-op (Fixed Term)
Relocation:
VISA Sponsorship:
Travel Requirements:
Flexible Work Arrangements:
Not Applicable
Shift:
Valid Driving License:
Hazardous Material(s):
Required Skills:
Automation Framework Design, Automation Framework Design, Business, cGMP Compliance, Change Management, Communication, Data Analysis, Electronic Records, Energy Saving Programs, Engineering Controls, Engineering Standards, Equipment Maintenance, Failure Mode and Effects Analysis FMEA, GMP Compliance, Lean Six Sigma Continuous Improvement, Maintenance Management, Maintenance Planning, Management Process, Manufacturing Quality Control, Mechatronics, Performance Improvement Plans, Process Design, Production Operations, Production Processes, Project Estimations {+ 5 more}
Preferred Skills:
Job Posting End Date:
07/4/2025
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.
Requisition ID:
R355134
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