QA Associate at Novartis

, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

24 Jul, 26

Salary

0.0

Posted On

25 Apr, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Management Systems, Good Manufacturing Practices, Documentation Review, Compliance, Quality Assurance, Standard Operating Procedures, CAPA, Quality Audits, Health Authority Inspections, Technical Knowledge, Data Integrity, Quality Metrics, Regulatory Compliance, Good Documentation Practice, Managing Ambiguity

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary Supports all GxP activities in the Quality department. Administers Quality Systems/ Processes including documentation, metrics and monitoring of actions and supports establishment of Quality operational processes. -Performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards. Supports Quality Projects and initiatives Job Description Major Accountabilities: Maintains applicable Standard Operating Procedures (SOPs), GxP compliant documentation and records within the Novartis Quality Management System. Ensures the integrity of all Quality Systems records and data, as applicable and collaboration of own team with other functions and departments -Ensures an adequate level of education, GxP knowledge . Updates and maintains relevant information in electronic systems (e.g.Change Control, Documentation, Training). Follow up and monitoring of e.g.CAPAs, actions, metrics, Quality plan). Supports Quality Audits and Health Authority inspections. Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Distribution of marketing samples (where applicable) Minimum Requirement Familiarity with Quality Management Systems is the pharmaceutical industry, Familiarity/experience within a Good Manufacturing Practices (GMP) atmosphere 1-2 years' experience in GMP documentation review, approval, and/or release would be ideal. Skills Desired Continued Learning, Good Documentation Practice, Guideline, Managing Ambiguity, Qa (Quality Assurance), Quality Management, Regulation, Self-Awareness, Technical Knowledge Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

The QA Associate supports GxP activities by administering quality systems, maintaining documentation, and monitoring metrics. They also ensure data integrity, manage CAPAs, and support quality audits and health authority inspections.