PLC Developer
at Katalyst Healthcares Life Sciences
North Haven, CT 06473, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 23 Jan, 2025 | Not Specified | 23 Oct, 2024 | 7 year(s) or above | Regulatory Standards,Communication Skills | No | No |
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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