Novartis
Overview
Join to apply for the
QA Associate (GMP Envinmt)
role at
Novartis . Base pay range
$33.00/hr - $33.00/hr This is a temporary contractor opportunity at Novartis. Magnit Global partners with Novartis to offer engaging temporary contractor opportunities. Responsibilities The candidate is responsible for hands-on, day-to-day cGMP activities as trained and scheduled. They interact directly with site staff (e.g., manufacturing, QC) to support the effort to produce quality products. This role ensures that the quality strategy is implemented and there is a continuous drive to improve product and process quality within the PU, QC labs, and other support areas. Ensure timely review of batch records for materials as instructed (e.g., media, apheresis, etc.). Interface closely with Process Units (PU) and QC to assist with batch record/QC data review, release, and compliance issue resolution. Review and audit production batch records and/or QC-related documentation to ensure adherence to Novartis policies, SOPs, and cGMP requirements. Participate in activities associated with event resolution and CAPAs. Implement and ensure adherence to applicable regulations and Novartis quality standards. Additional activities may be assigned for training and completion as required. Demonstrate and role-model the Novartis values and behavior.
Qualifications
2-3 years of GMP and GDP experience 2-3 years of Batch Record Review
Location
Morris Plains, NJ (onsite) Schedule
1 shift - Sun-Wed 9:00 AM - 7:00 PM (x1); 2 shift - Wed-Sat 9:00 AM - 7:00 PM (x2) Pay
$30 to $33/hr (W2 Only) Contract type
6-month Benefits
Health, dental, vision, 401(k) 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. Together we can achieve breakthroughs that change patients lives. Ready to create a brighter future? 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. Job details
Seniority level: Not Applicable Employment type: Contract Job function: Quality Assurance Industries: Pharmaceutical Manufacturing #J-18808-Ljbffr
Join to apply for the
QA Associate (GMP Envinmt)
role at
Novartis . Base pay range
$33.00/hr - $33.00/hr This is a temporary contractor opportunity at Novartis. Magnit Global partners with Novartis to offer engaging temporary contractor opportunities. Responsibilities The candidate is responsible for hands-on, day-to-day cGMP activities as trained and scheduled. They interact directly with site staff (e.g., manufacturing, QC) to support the effort to produce quality products. This role ensures that the quality strategy is implemented and there is a continuous drive to improve product and process quality within the PU, QC labs, and other support areas. Ensure timely review of batch records for materials as instructed (e.g., media, apheresis, etc.). Interface closely with Process Units (PU) and QC to assist with batch record/QC data review, release, and compliance issue resolution. Review and audit production batch records and/or QC-related documentation to ensure adherence to Novartis policies, SOPs, and cGMP requirements. Participate in activities associated with event resolution and CAPAs. Implement and ensure adherence to applicable regulations and Novartis quality standards. Additional activities may be assigned for training and completion as required. Demonstrate and role-model the Novartis values and behavior.
Qualifications
2-3 years of GMP and GDP experience 2-3 years of Batch Record Review
Location
Morris Plains, NJ (onsite) Schedule
1 shift - Sun-Wed 9:00 AM - 7:00 PM (x1); 2 shift - Wed-Sat 9:00 AM - 7:00 PM (x2) Pay
$30 to $33/hr (W2 Only) Contract type
6-month Benefits
Health, dental, vision, 401(k) 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. Together we can achieve breakthroughs that change patients lives. Ready to create a brighter future? 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. Job details
Seniority level: Not Applicable Employment type: Contract Job function: Quality Assurance Industries: Pharmaceutical Manufacturing #J-18808-Ljbffr