~~~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...
QC Analyst - GMP

The QC Analyst is responsible for performing tasks associated with release testing and reviewing laboratory data. Communicating with and supporting internal & external partners of the Quality Control organization.

Key Responsibilities:
• Provide support to peers within the Quality Assurance, Quality Control and AS&T teams. 
• On-time and GMP-compliant release of patient batches
• Support Quality Control and AS&T as a valued business partner, with a culture of safety, quality, 
delivery to patients, cost, compliance, and data integrity. 
• Author, review and support procedures, investigations, corrective and preventive actions, change 
controls, complaints, and training as it relates to quality control testing. 
• Ensure that QC testing is properly conducted and documented for all performed activities, with 
emphasis on Data Integrity. Evaluate and approve QC records as required. 
• Provide oversight and monitoring of quality control KPIs and programs. 
• Perform QC related validations, transfers, improvements, investigations related activities (deviations, OOS, OOE, OOT, CAPAs, trending), and Change Control systems. 
• Prepare and participate in health authorities’ inspections and internal audits of QC. Ensure quality control area is inspection ready.

Please note:
• This position may involve shift work which will be defined through site commercialization needs. 
• This position may involve on-call shifts, if required, when scheduled.

Essential Requirements:
• BSc in Chemistry or relevant scientific
• 3+ years of experience in a GMP quality control environment 
• Strong HPLC experience a must
• General HSE Knowledge 
• Knowledge of GMP Manufacturing Process Execution 
• Quality Control (QC) Testing 
• Quality Control Sampling

Location: Indianapolis, IN (Onsite)
Pay Rate: $37 - $40hr based on experience and qualifications (W2 Only)
Contract: 12+-month 
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 [email protected].