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QA Associate

Quality Control
Batch Record
Manufacturing Operations
Operations
Document Control
Reconciliation
CGMP
Quality Assurance
GMP
QA
Description:

~~~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... 
QA Associate

Note- Start with Normal day Shift, shift timing may change after 6 months.
Responsibilities include but are not limited to:
• Responsible for support of manufacturing operations such as batch record issuance and reconciliation activities.
• Review of GMP documentation, which includes conducting independent documentation review of executed cGMP records.
• Release of incoming material
• Work closely with the production, quality control and supply chain departments to ensure their practice fully adheres to GDP practices and procedures.
• Supports establishment of systems and work streams compliant with approved site procedures and GDP associated with the sites batch record documentation.
• Key Performance Indicator (KPI) tracking and reporting for the established work streams.
• Work closely with Document Control to ensure appropriate handover of GMP executed records.

The ideal candidate will bring the following to the role:
-Bachelors Degree Preferred; Biology and/or microbiology background also highly preferred.
-Minimum 2 years of experience in GMP manufacturing required
-Experience with cGMP systems and practices, preferable involving document control, quality assurance, or quality systems.
-Maintain Weekly and Daily targets to support the QA Operations team goals. This includes working in an organized fashion.
-Ability to gown aseptically and work in controlled non-classified areas.

Location: Millburn, NJ (Onsite)
Pay Rate: $29.12 - $31.82/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.
 

QUALIFICATION/ LICENSURE :
  • Work Authorization : Green Card, US Citizen, Other valid work visa
  • Preferred years of experience : 2+ Years
  • Travel Required : No travel required
  • Shift timings: Onsite: Millburn, NJ
Job Location Millburn, New Jersey
Pay USD 29.12 - USD 31.82 Per Hour
Contract Duration 12 month(s)