Electrical and Controls Engineering Technician

United Kingdom

Sharp Services, LLC
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Electrical and Controls Engineering Technician

Apply locations Macungie time type Full time posted on Posted Yesterday job requisition id JR31082

The Electrical and Controls Engineering Technician position supports the serialization team in data and project work.

ESSENTIAL DUTIES AND RESPONSIBILITIES:

  1. Accurately enter data related to product configurations within the Sharp Electronic Product Code Information Services and site level serialization systems.
  2. Ensure all entered data follows consistent formatting and standards, based upon existing Sharp procedures, to maintain uniformity and facilitate easy data retrieval and analysis.
  3. Adhere to all regulatory and Sharp specific requirements for data entry.
  4. Generate and provide reports based upon EPCIS and site level data to allow for analysis, decision-making, troubleshooting and compliance purposes.
  5. Assist in equipment installation, qualification and commissioning activities.
  6. Ability to read and understand electrical schematics, mechanical drawings, and OEM technical documents.
  7. Support Engineers with the implementation of technical projects for new equipment such as high speed automated packaging equipment.
  8. Implement serialization configurations and product/manufacturer data within Sharp's entire serialization solution from EPCIS to line level devices.
  9. Ability to author technical documents such as Change Controls and WRKI's, Review MPR's etc.
  10. Help train and develop new technician hires.
  11. Initiate parts requisition order for parts and machines.
  12. Assist in maintaining and replenishing a spare parts inventory for all equipment within the scope of responsibility.
  13. Perform electromechanical troubleshooting including fuse testing, motor and relay replacement, and robotic component handling systems, PLC controllers, sensors, setup and adjustment of online printing, barcode scanning, and OCR/OCV vision equipment.
  14. Perform routine backups of PLC and HMI programs.

QUALIFICATIONS:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Ability to perform technical analysis of root cause and corrective action establishment during event investigations.

Ability to take ownership and drive corrective actions including documentation updates, Change Control development, and equipment system upgrades.

Ability to travel internationally as part of an extended team to support new equipment purchases when necessary.

SUPERVISORY RESPONSIBILITIES:

None

PREFERRED / REQUIRED EDUCATION and/or EXPERIENCE:

5 years of pharmaceutical packaging and serialization experience is preferred along with a minimum of an associate's degree in a related technical field.

About Us

Sharp Packaging Services works across the world to create unique commercial and clinical packaging solutions for the pharmaceutical and biotechnology industry.

We are made up of two dynamic international divisions, Sharp Packaging Solutions and Sharp Clinical Services. Together our 1,600-strong team works from state-of-the-art facilities in the United States, United Kingdom, Belgium and the Netherlands.

We've built an exceptional global reputation for the design, serialization and production of innovative, cost-effective compliance packaging for even the most complex products.

Our extensive range includes blister packs, bottles, pouches and stick packs, but our expertise goes far beyond, enabling us to support your product through every stage of design, development, manufacture and delivery.

Our clinical services division is one of the world's leading providers of innovative clinical supply chain services, with a talented and highly experienced team that can handle every aspect of your supply chain. Our work spans everything from drug development and manufacturing to clinical supplies packaging, labelling, distribution, Qualified Person auditing and comparator sourcing.

Date Posted: 25 April 2025
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