Key Responsibilities:
Design, develop, configure and commission PLC, SCADA or other automation system.
Perform installation, configuration and troubleshooting of Windows OS migration for GMP computerised system.
Draft and execute commissioning and qualification documentations such as for FAT, UAT, test script and IOQ.
Support system architecture design, data integrity assessment, electronic records and electronic signature assessment, specification development, control strategies and library development.
Contribute to change management, deviation / non-conformance and system documentations.
Support Computer System Validation (CSV) activities.
Support system integration and related deliverables.
Requirements:
Hold Bachelor’s degree in Life Sciences, Engineering or related field.
Have worked for at least 2 years in pharmaceutical, medical device or related environment.
Have experience in configuring and commissioning of PLC, SCADA and/or other automation systems.
Have experience in Windows OS especially in OS migration.
Have worked with automation hardware and OT shop floor technologies.
Understand pharmaceutical manufacturing and IT/OT operations.
Understand computerised system requirements in the pharmaceutical industry (e.g., 21 CFR Part 11, Annex 11) and industry best practice documents / standards (e.g., GAMP5, ISA 88, ISA 95).
Understand SDLC and quality management requirements of the pharmaceutical industry.
Preferably with relevant training and certifications.
Why Join Orka:
Work that Matters:
Support clients bringing innovative and life saving solutions to the population.
Career Development:
Build a consulting career in a professional consulting company with Life Sciences focus.
Professional Environment:
Work with similar professionals possessing
Intelligent, Resourceful, Loyal and Teamwork
characteristics.
Impactful Learning and Mentoring:
Develop yourself in an environment that heavily foster learning attitude and benefit from access to training materials, references, mentors and management with wide range of regulated industry experiences.
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