DSJ Global
Global Sales Operations Manager at Phaidon International
We are seeking a highly skilled
Senior Automation Engineer
to join a
biotech manufacturing team . This role will be responsible for designing, implementing, and maintaining automation systems, including
PLC, SCADA, and MES , to support bioprocessing and manufacturing operations. The ideal candidate will have a strong technical background in industrial automation, experience in regulated environments (GMP), and the ability to lead automation projects from concept to completion. Key Responsibilities:
Design, develop, and maintain
PLC, SCADA, and MES
systems for biotech manufacturing processes.
Lead automation projects, including system upgrades, modifications, and new installations.
Collaborate with cross-functional teams, including
process engineering, IT, and quality assurance , to integrate automation solutions with biotech manufacturing processes.
Ensure compliance with
GMP, FDA, and other regulatory standards
in automation system design and implementation.
Perform troubleshooting, root cause analysis, and corrective actions for automation-related issues.
Develop and maintain documentation, including
functional specifications, validation protocols, and standard operating procedures (SOPs) .
Support
data integrity, cybersecurity, and system validation
efforts related to automation systems.
Train and mentor junior engineers and technicians on automation best practices and system operation.
Required Qualifications:
Bachelor's or Master's degree
in Electrical Engineering, Automation, Computer Science, or a related field.
5+ years
of experience in automation engineering within a
biotech, pharmaceutical, or life sciences manufacturing environment .
Expertise in
PLC programming (Allen-Bradley, Siemens, or similar) , SCADA systems (Ignition, Wonderware, or equivalent), and MES platforms.
Strong understanding of
cGMP, 21 CFR Part 11, and validation requirements
for automation systems.
Experience with
industrial communication protocols
(Ethernet/IP, Profibus, Modbus, OPC, etc.).
Knowledge of
historians, data analytics, and integration with enterprise systems (ERP, LIMS, etc.)
is a plus.
Seniority level
Mid-Senior level Employment type
Full-time Job function
Industries: Chemical Manufacturing
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We are seeking a highly skilled
Senior Automation Engineer
to join a
biotech manufacturing team . This role will be responsible for designing, implementing, and maintaining automation systems, including
PLC, SCADA, and MES , to support bioprocessing and manufacturing operations. The ideal candidate will have a strong technical background in industrial automation, experience in regulated environments (GMP), and the ability to lead automation projects from concept to completion. Key Responsibilities:
Design, develop, and maintain
PLC, SCADA, and MES
systems for biotech manufacturing processes.
Lead automation projects, including system upgrades, modifications, and new installations.
Collaborate with cross-functional teams, including
process engineering, IT, and quality assurance , to integrate automation solutions with biotech manufacturing processes.
Ensure compliance with
GMP, FDA, and other regulatory standards
in automation system design and implementation.
Perform troubleshooting, root cause analysis, and corrective actions for automation-related issues.
Develop and maintain documentation, including
functional specifications, validation protocols, and standard operating procedures (SOPs) .
Support
data integrity, cybersecurity, and system validation
efforts related to automation systems.
Train and mentor junior engineers and technicians on automation best practices and system operation.
Required Qualifications:
Bachelor's or Master's degree
in Electrical Engineering, Automation, Computer Science, or a related field.
5+ years
of experience in automation engineering within a
biotech, pharmaceutical, or life sciences manufacturing environment .
Expertise in
PLC programming (Allen-Bradley, Siemens, or similar) , SCADA systems (Ignition, Wonderware, or equivalent), and MES platforms.
Strong understanding of
cGMP, 21 CFR Part 11, and validation requirements
for automation systems.
Experience with
industrial communication protocols
(Ethernet/IP, Profibus, Modbus, OPC, etc.).
Knowledge of
historians, data analytics, and integration with enterprise systems (ERP, LIMS, etc.)
is a plus.
Seniority level
Mid-Senior level Employment type
Full-time Job function
Industries: Chemical Manufacturing
#J-18808-Ljbffr