DeltaV Engineer
1 month ago
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.
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.
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