DeltaV Engineer

Main Responsibilities:

• Duration will be – starting as early as Sep 2023, ending Jun 2024. (potential to extend longer)
• Draft SDLC document (automation specific) such as configuration specification, automation IQ, automation OQ, etc.
• Execute Automation IQ and Automation OQ in the field.
• Identify issues during the AIQ/AOQ execution and resolve to correction via a change control
• Open/close change control including drafting of the change control, make/follow the correction, update documents as needed following the change control procedure.
• Draft requirement traceability
• list of equipment in the scope are vial/syringe filling line, Lyophilizer, isolator, glove tester, autoclave, parts washer, sterilizer, BAS to name a few.

All potential candidates should read through the following details of this job with care before making an application.

Desired - Experience and Education:

• 2-3 years in Automation validation experience in pharmaceutical, GMP environment.
• Good written and verbal communication skills. Professional, detail-orientated.
• Able to work in a group and independently.

Salary: Competitive Salary offerings

Benefits: Paid Leave, 401-K, Group Medical, Dental, Vision, Life, AD&D, etc.