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Building Automation Systems Engineer, Pharmaceutical

Location : Valley Cottage NY US 10989
Job Type : Direct
Reference Code : 20439-MK1
Compensation : 80000.00 - 100000.00 USD/YEAR
Start Date : 02/10/2021
Hours : Full Time
Required Years of Experience : 5
Required Education : BS Mechanical, Electrical or Industrial Engineering
Travel : No
Relocation : No
Job Industry : Pharmaceutical

Job Description :


  • Permanent position for a Building Automation Systems Engineer providing technical manufacturing support for existing and new equipment, processes and for designing developing and introducing new processes and equipment from conception through qualification.

  • Perform high level Building Automation System software and hardware troubleshooting on complex HVAC systems and subsystems including network and controllers.

  • New building equipment commissioning & existing building retro commissioning.

  • Fine-tuning systems through testing and evaluation procedures.

  • Test and evaluate the mechanical and building automation systems of industrial buildings to ensure these systems operate as designed and constructed, and make recommendations to improve efficiency.

  • Apply knowledge of control theory, automatic temperature controls, building automation systems, and other building subsystems.

  • Integrate low voltage building sub-systems.

  • Apply knowledge of microcontroller programming, binary and digital logic, and analog circuits.

  • Supervise the installation and maintenance of building automation systems that create centralized controls for such features as a building's lighting system, heating and cooling system, and water heating system.

  • Inspect, test, adjust, and balance heating, cooling, and ventilating systems in commercial and industrial buildings to achieve performance standards specified in the design of the system.

  • Optimize process yield and productivity through continuous improvement programs.

  • Manage pharmaceutical technical transfers including all relevant activities that need to be performed to manufacture, control and measure product quality.

  • Provide technical management, integration, and development of new and existing equipment and automated processes.

  • Commission new equipment using well planned, documented, and managed engineering approach to the start-up and turnover of facilities, systems, and equipment to the Production Department that results in a safe and functional environment that meets established design requirements and stakeholder expectations.

  • Assist in the design of new equipment, processes, procedures and systems.

  • Purchase and install new or transferred equipment.

  • Arrange and lead in the overhauling of existing equipment.

  • Investigate manufacturing problems to diagnose to root cause and recommend lasting solutions.

  • Understand CMMS and OEE software, to help organize and assemble data and assign action items.

  • Establish through calculation and analysis production capacities

  • Ensure compliance with all applicable specifications, standard operating procedures (SOPs), and FDA.


 


Required Qualifications :


  • BS in Mechanical Engineering, Industrial Engineering or Electrical Engineering.

  • Minimum 2 years of experience in Medical Device Manufacturing, Pharmaceutical, or FDA regulated environment.

  • Knowledge and experience operating under OSHA standards.

  • Knowledge of or trained in Lean Manufacturing / Six Sigma.

  • Minimum 5 years of experience working with third-party vendors, contractors and service providers required.

  • Demonstrated experience managing a biotech facility, including a combination of manufacturing, research, and office space.

  • Experience scaling operations and building new space is preferred.

  • Experience with CMMS - Computerized Maintenance Management System.

  • Experience with maintenance of manufacturing utilities, including steam, compressed air, process instrumentation, electrical, plumbing, carpentry and HVAC systems.

  • Experience with SAP and MS Office.

  • Thorough understanding of cleanrooms and cGMP.

  • Ability to read blue prints and schematics, and to use shop tools.

  • Detail oriented, rigorous, analytical, reactive, and good interpersonal skills.

  • Experience with PFMEA, FAT, SAT, IQ, OQ, and PQ.

  • Experience generating technical documentation for maintenance operations such as work instructions for production processes.

  • Ability to travel domestically and internationally.



Contact: Monique Kleiman


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Please send all inquiries to 
MK@EngineeringResource.com


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