Qa Operations Specialist
Singapore, Singapore
Job Description
More than 380! That’s the number of associates in our Singapore Large Molecules division to support the making of medicines for our patients worldwide.
Key Responsibilities
- Enable Quality oversight to site operations/objectives
- Perform and be responsible in ensuring Batch record review and release is in full cGMP compliance to regulatory and Novartis Quality Standards
- Provide support in ensuring a smooth manufacturing operations, in handling deviations/capa, change control, complaints, customer management, escalation, recall etc are in full cGMP compliance to regulatory and Novartis Quality Standards
- Provide support in ensuring success to new product launches or transfer and product lifecycle management are in full cGMP compliance to regulatory and Novartis Quality Standard
- Any other task/duties assigned by Line Manager
Commitment to Diversity & Inclusion:
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum requirements
- Bachelor Degree in Science and related work experience in Pharmaceutical GMP manufacturing environment. Diploma holders can be considered with additional years of work experience.
- 6 – 10 years of relevant experience in pharmaceutical manufacturing in QA Operations, supporting audit, batch record review and release
- Good proficiency in English and good experience working in a team.
Division
Novartis Technical Operations
Business Unit
NTO QUALITY
Country
Singapore
Work Location
Singapore
Company/Legal Entity
NOV SINGAPORE PHARMA MANUFG
Functional Area
Quality
Job Type
Full Time
Employment Type
Regular
Shift Work
No
Early Talent
No
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Job Detail
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Job IdJD1145261
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IndustryNot mentioned
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Total Positions1
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Job Type:Full Time
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Salary:Not mentioned
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Employment StatusPermanent
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Job LocationSingapore, Singapore
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EducationNot mentioned