Novartis
QA Associate Deviation Novartis (Contract)
This temporary contractor opportunity at Novartis is for a
QA Associate Deviation
role. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range $33.00/hr - $33.00/hr Important note:
This is a temporary contractor opportunity at Novartis. Novartis partners with Magnit Global to offer engaging temporary contractor opportunities. Read on to learn more and determine if this role is right for you. Ready to work with/through Magnit at Novartis?
The candidate is responsible for hands-on, day-to-day cGMP activities as trained and required per schedule. They interact directly with site staff in support of manufacturing, QC, and other operations to produce quality products. This role ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the PU, QC labs, and other support areas while adhering to Novartis policies, SOPs, and cGMP requirements. Duties Initiation, review and approval of initials & impact assessment, deviation (focus on minor and major), quality event and OOS/OOE/OOT investigations and CAPA plan establishment in accordance with applicable SOPs. Participates in activities associated with event resolution and CAPAs. Implements and ensures adherence to appropriate regulations and Novartis quality standards. Experience 3 to 5 years of deviation experience. Experience with writing documentation, GMP, GDP. Additional activities may be assigned for training and completion as required. Demonstrates and role models the Novartis values and behaviors. Location
Morris Plains, NJ (onsite) Shift
Mon-Fri: 9 AM 5 PM Pay Rate
$30 to $33/hr based on experience and qualifications (W2 Only) Contract
6 months Benefits
Health, dental, vision, 401k Why Novartis Helping people with disease and their families requires a community of smart, passionate people. Collaborating, supporting and inspiring each other helps achieve breakthroughs that change patients lives. 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, or any pre-employment testing, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com. Seniority level
Not Applicable Employment type
Contract Job function
Quality Assurance Industries
Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Novartis. Get notified about new Quality Assurance Associate jobs in Morris Plains, NJ. #J-18808-Ljbffr
This temporary contractor opportunity at Novartis is for a
QA Associate Deviation
role. Your actual pay will be based on your skills and experience talk with your recruiter to learn more. Base pay range $33.00/hr - $33.00/hr Important note:
This is a temporary contractor opportunity at Novartis. Novartis partners with Magnit Global to offer engaging temporary contractor opportunities. Read on to learn more and determine if this role is right for you. Ready to work with/through Magnit at Novartis?
The candidate is responsible for hands-on, day-to-day cGMP activities as trained and required per schedule. They interact directly with site staff in support of manufacturing, QC, and other operations to produce quality products. This role ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the PU, QC labs, and other support areas while adhering to Novartis policies, SOPs, and cGMP requirements. Duties Initiation, review and approval of initials & impact assessment, deviation (focus on minor and major), quality event and OOS/OOE/OOT investigations and CAPA plan establishment in accordance with applicable SOPs. Participates in activities associated with event resolution and CAPAs. Implements and ensures adherence to appropriate regulations and Novartis quality standards. Experience 3 to 5 years of deviation experience. Experience with writing documentation, GMP, GDP. Additional activities may be assigned for training and completion as required. Demonstrates and role models the Novartis values and behaviors. Location
Morris Plains, NJ (onsite) Shift
Mon-Fri: 9 AM 5 PM Pay Rate
$30 to $33/hr based on experience and qualifications (W2 Only) Contract
6 months Benefits
Health, dental, vision, 401k Why Novartis Helping people with disease and their families requires a community of smart, passionate people. Collaborating, supporting and inspiring each other helps achieve breakthroughs that change patients lives. 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, or any pre-employment testing, please direct your inquiries to Magnit at directsourceproteam@prounlimited.com. Seniority level
Not Applicable Employment type
Contract Job function
Quality Assurance Industries
Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Novartis. Get notified about new Quality Assurance Associate jobs in Morris Plains, NJ. #J-18808-Ljbffr