Description
393987BREquipment Specialist I:
Singapore
About the role
Location - Singapore
About the Role:
Execute assigned Manufacturing tasks and activities according to production schedule to enable the timely production of products with quality and quantity in compliance with the relevant GMP, safety and environmental guidelines.
Key Responsibilities:
- Participation to the manufacturing processes. Perform all Equipment Operator Tasks/Responsibilities.
- Suggest improvement actions (organization, process, safety, hygiene, etc.) at shop floor
- Review and approval of analytical data / tests (analytical release) Suggest improvement actions (organization, process, safety, hygiene, etc.) at shop floor Documentation Specialist GMP
- Prepare, print and consolidate the batch documents, labels... and handover to production operators within the deadlines set according to the production schedule
Commitment to Diversity & Inclusion:
- Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve._
Role Requirements
Essential Requirements:
- 35 years' experience in Pharma/Manufacturing sector in analytical lab in a GMP environment/equivalent.
- Able to understand changing dynamics of pharmaceutical industry Collaborating across boundaries.
- Expertise in GxP operations. Operations Management and Execution.
- Associate to work on 12hrs rotating shift work in Downstream Process.
Desirable Requirements:
- Working experience within the pharmaceutical industry
Division
Operations
Business Unit
CONTRACT MANUFACTURING
Work Location
Singapore
Company/Legal Entity
NOV SINGAPORE PHARMA MANUFG
Functional Area
Technical Operations
Job Type
Full Time
Employment Type
Regular
Shift Work
Yes
Early Talent
No
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