What are the responsibilities and job description for the Deviation Writer position at Novartis?
:::Please note: This is a temporary contractor opportunity at Novartis :::
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!
Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com
Ready to work with/through Magnit at Novartis? Please read on...
Deviation Writer
To author deviations related to facilities and engineering processes, equipment and areas. This includes the initiation, investigation, authoring, identifying correct CAPAs and effectiveness checks of those CAPA's and throughout meeting required timelines.
Major Accountabilities:
Deviations, Investigations, and CAPAs:
Education:
BSc. in Engineering or equivalent scientific degree.
Languages:
Fluent in speaking / writing in English
Experience:
Minimum 3 years' experience in GMP manufacturing role with 1 year of deviation/root cause analysis experience.
Location: Morris Plains, NJ (Onsite)
Pay Rate: $42 - $52/hr based on experience and qualifications (W2 Only)
Contract: 12 months
Health, dental, vision, 401k
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accommodation:
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.
Novartis touches the lives of a tenth of the world’s population. Every role here, regardless of contract type, makes an impact on human life!
Novartis US partners with external managed service provider Magnit Global to offer engaging temporary contractor opportunities like this, to those who are looking for flexibility in their career while looking to gain new skills and experiences providing services to an inclusive global medicines company. Click here to learn more about Magnit www.magnitglobal.com
Ready to work with/through Magnit at Novartis? Please read on...
Deviation Writer
To author deviations related to facilities and engineering processes, equipment and areas. This includes the initiation, investigation, authoring, identifying correct CAPAs and effectiveness checks of those CAPA's and throughout meeting required timelines.
Major Accountabilities:
Deviations, Investigations, and CAPAs:
- Initiate deviations within required timelines.
- Support the facilities team in the triage of unexpected events.
- Author investigations for facilities and engineering related deviations within required timelines.
- Work cross-functionally to assess deviation impact and identify root causes.
- Use equipment/facility knowledge and root cause investigation tools to analyze data and to identify root
- Work collaboratively in the design CAPAs and CAPA effectiveness checks to eliminate/mitigate deviations.
- Support the process of escalation of deviations when appropriate according to escalation guidelines. Present
- Provides support for all internal or external audits.
- Opening, and closing of deviations within required timeframes
- Closing of CAPAs within required timeframe
- Effectiveness of CAPAs
- Success rate of internal audits and Health Authorities' inspections
Education:
BSc. in Engineering or equivalent scientific degree.
Languages:
Fluent in speaking / writing in English
Experience:
Minimum 3 years' experience in GMP manufacturing role with 1 year of deviation/root cause analysis experience.
Location: Morris Plains, NJ (Onsite)
Pay Rate: $42 - $52/hr based on experience and qualifications (W2 Only)
Contract: 12 months
Health, dental, vision, 401k
Why Novartis:
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together?
EEO Statement:
The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.
Accommodation:
If you require reasonable accommodation in completing this application, interviewing, completing any pre-employment testing, or otherwise participating in the employee selection process, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com.
Salary : $42 - $52
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