Associate Manufacturing Systems

Quality Consulting Group

  • Juncos, PR
  • Temporal
  • Tiempo completo
  • Hace 1 mes
QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.Responsibilities:
  • Assists with or directly provides technical engineering support in process optimization strategies, upgrades, replacements, and modifications in the operations, manufacturing or pilot plant environment.
  • Ensures that all operations are accomplished in a safety and compliant manner consistent with current corporate policies, industry standards, and applicable regulatory requirements.
  • Perform standard engineering work requiring application of standard techniques and procedures.
  • Monitor operations of a unit operation or system and actively assist operations, maintenance or project personnel as required.
  • Routinely audit the operational performance and regulatory compliance of a limited number of equipment items or systems of minor to moderate complexity.
  • Routinely troubleshoot operational issues with individual equipment or skids.
  • Assist with the proposal, initiation, testing and implementation of proposed changes to process, utility and/or facility systems.
  • Assist more senior engineers in the evaluation and implementation of engineering improvements, policy changes, compliance improvements and optimization programs.
  • Maintain and troubleshoot all systems, electrical and mechanical.
  • Acting as a technical resource to plant personnel.
Qualifications:
  • Bachelor's degree or Associate Degree in Electronic Engineering Technology or related area
  • Experience in operations/manufacturing environment preferred.
  • Exposure to or direct experience with regulated environments (i.e. cGMP, OSHA, EPA) preferred.
  • Working knowledge of pharmaceutical/biotech processes
  • Familiarity with validation processes, documentation in a highly regulated environment
  • Ability to learn, install, maintain, and troubleshoot relay logic, ladder diagrams, control components, photo eyes, motor starts, relays, limit switches, proximity sensors, timers, solenoids and frequency inverters.
  • Understanding in Automation systems like vision systems (Systech and/or Cognex), sensor, PLC, robotic, lasers printers.
  • Understanding in PLC (Rockwell and/or Siemens, Systech Serialization, Packaging Equipment).
  • Understanding in Siemens and Rockwell HMI’s.
  • Understanding in sensors and pneumatic
  • Experience in SCADA/ PLC Control System in regulated manufacturing environment
  • Availability for 12hrs Shifts (5:00 am to 5:30 pm or 5:00pm to 5:00 am included alternate weekend)
Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity,, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

Quality Consulting Group

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