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Associate Mfg Systems

Company: BioPharma Consulting JAD Group

Job Location: Juncos, Juncos, Puerto Rico

Job Type: CONTRACT - (ON_SITE)

Date Posted: April 05, 2025

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In a Full Automation role, Under close supervision, 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.

Key Responsibilities:

Operations Engineering:

  • Monitor unit operations and assist production, maintenance, or project teams as needed.
  • Audit operational performance and regulatory compliance of equipment and systems.
  • Troubleshoot operational issues with equipment, skids, and systems.
  • Assist in proposing, testing, and implementing process, utility, and facility system improvements.
  • Support senior engineers in policy updates, compliance improvements, and optimization programs.
  • Maintain and troubleshoot electrical and mechanical systems.
  • Learn, install, maintain, and troubleshoot relay logic, ladder diagrams, and control components such as photo eyes, motor starters, relays, limit switches, proximity sensors, timers, solenoids, and frequency inverters.
  • Troubleshoot PLC programs (ladder logic, CPU, I/O boards, counters, modules, devices, and communication modules such as Ethernet).
  • Provide ongoing plant support, including troubleshooting and developing new automation functions.
  • Act as a technical resource for plant personnel.

Required Education & Experience:

  • Bachelor’s degree in Engineering or Engineering Technology.
  • Exposure to or direct experience in operations/manufacturing environments preferred.
  • Familiarity with regulated environments (cGMP, OSHA, EPA) preferred.

Preferred Qualifications:

  • Engineering or Engineering Technology background.
  • Experience with PLC programming, Allen-Bradley, and Vision Systems.
  • Working knowledge of pharmaceutical/biotech processes.
  • Familiarity with validation processes and documentation in regulated environments.
  • Ability to operate specialized laboratory equipment and computers.
  • Strong verbal communication skills in English and Spanish.
  • Ability to interpret and apply GLP and GMP standards.
  • Problem-solving skills with applied engineering knowledge.
  • Experience with technical report writing and presentations.
  • Computer literacy and ability to work with robotic and production equipment.
  • Interest in mathematics, physics, and mechanical systems.
  • Ability to work both independently and as part of a team in a fast-paced environment.

Work Environment:

  • 12-hour night shifts (5:00 PM – 5:30 AM).
  • Ability to stand/walk for up to 10-12 hours.
  • Must be self-motivated, customer-centric, and committed to safety and compliance.

Push yourself, because no one else is going to do it for you.

“Les Brown”
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