CSV Engineer

Hyde Engineering + Consulting; Hyderabad; On-site; INR 800,000 - 1,200,000; Full time

Job summary

A global engineering consultancy is seeking a CSV/Automation Engineer in Hyderabad with 5-10 years of experience in the pharma industry. The role involves leading automation projects, troubleshooting control systems, and working closely with engineering leads. A valid passport for travel and an engineering degree in a relevant field is required. This is a full-time position offering significant responsibilities in process automation engineering.

Qualifications

• 5 to 10 years of experience in multinational pharma/biopharma companies.
• Experience with DCS/PLC/SCADA/BMS systems.
• Knowledge of industry guidelines for GMP regulated environments.

Responsibilities

• Lead Automation Projects including DCS/PLC/SCADA.
• Troubleshoot automation and control systems.
• Ensure successful completion of FAT, SATs, IQ, OQ.

Skills

Process automation engineering

Automation platforms knowledge (Delta V, Honeywell, etc.)

Strong organizational skills

Excellent communication skills

Proficiency with Microsoft Office

Education

Engineering degree in Automation, Instrumentation, EEE, ECE

Job description

Overview

Position: CSV/Automation Engineer
Employer: Hyde Engineering + Consulting

Responsibilities

• 5 to 10 years of experience in multinational pharma/biopharma companies with hands on experience in Process automation engineering


• Experience in designing and implementation/testing/commissioning/Qualification of (DCS/PLC/SCADA/BMS/EMS systems)


• Experience in trouble shooting for automation and control systems


• Drive and Lead Automation (DCS/PLC/SCADA/BMS) Projects


• Technical understanding and experience in automation platforms, such as Delta V, Honeywell, Rockwell PLC, Siemens XFP


• Facilities, Utilities, and Equipment (FUE) qualification; Unit operations automation qualification with Honeywell, Delta V, and PLC-based systems; Computerized systems validation


• Support to change controls, investigations, deviations, and CAPAs


• Ability to effectively lead validation projects, coordinate contractors, junior level personnel and drive results


• Working closely with the systems integrators, automation leads & process leads


• Completing the FAT, SATs, IQ, OQ; creating and executing the protocols & documentation


• Knowledge of E2500, V Model concepts along with GAMP5, S88, S95


• Knowledge of Industry guidelines (ISPE, PDA), US and international regulations (FDA, ICH, ISO, EU) for GMP regulated environments


• Must be able to solve routine problems with assistance. Strong organizational skills, excellent writing and communications skills


• Proficiency with Microsoft Office including Word, Excel, and PowerPoint; Microsoft Project and Visio a plus


• Ability to travel up to 50% or more within and outside Malaysia


• Large scale project experience


• Valid Passport with no restrictions to travel

Education

• Engineering degree in Automation, Instrumentation, EEE, ECE

Seniority level

• Mid-Senior level

Employment type

• Full-time

Job function

• Consulting and Engineering

Industries

• Pharmaceutical Manufacturing