PLC Developer

at  Katalyst Healthcares Life Sciences

North Haven, CT 06473, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate23 Jan, 2025Not Specified23 Oct, 20247 year(s) or aboveRegulatory Standards,Communication SkillsNoNo
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Description:

Responsibilities:

  • Design, develop, and troubleshoot automated systems using Rockwell Controls, SCARA robots, and Cognex/Keyence Vision Systems.
  • Conduct Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for pharmaceutical and medical device machinery to ensure compliance with industry standards.
  • Prepare and review User Requirement Specifications (URS) for automated systems.
  • Ensure compliance with regulatory requirements, including 21CFR Part 11 and NFPA-79.
  • Provide support in PLC program troubleshooting and ensure continuous system improvements.
  • Collaborate with cross-functional teams to optimize automation processes and equipment performance.
  • Work with internal and external stakeholders to execute validation plans, ensuring timely and effective delivery of projects.

Qualifications:

  • 5-7+ years of experience in automation engineering, with a focus on pharmaceutical or medical device manufacturing.
  • Proficiency in Rockwell Controls (Allen-Bradley PLCs, etc.).
  • Hands-on experience with Cognex/Keyence Vision Systems and SCARA robots.
  • Strong understanding of validation protocols, specifically IQ/OQ/PQ for regulated environments.
  • Knowledge of regulatory standards including 21CFR Part 11 (electronic records compliance) and NFPA-79 (electrical standards).
  • Strong problem-solving skills and experience in PLC program troubleshooting.
  • Excellent written and verbal communication skills.

Responsibilities:

  • Design, develop, and troubleshoot automated systems using Rockwell Controls, SCARA robots, and Cognex/Keyence Vision Systems.
  • Conduct Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for pharmaceutical and medical device machinery to ensure compliance with industry standards.
  • Prepare and review User Requirement Specifications (URS) for automated systems.
  • Ensure compliance with regulatory requirements, including 21CFR Part 11 and NFPA-79.
  • Provide support in PLC program troubleshooting and ensure continuous system improvements.
  • Collaborate with cross-functional teams to optimize automation processes and equipment performance.
  • Work with internal and external stakeholders to execute validation plans, ensuring timely and effective delivery of projects


REQUIREMENT SUMMARY

Min:7.0Max:12.0 year(s)

Pharmaceuticals

Engineering Design / R&D

Clinical Pharmacy, Software Engineering

Graduate

Proficient

1

North Haven, CT 06473, USA