QC Supervisor
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![]() United States, New Jersey, Millburn | |
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Job Description Summary The QC Supervisor is responsible for day-to-day oversight of Quality Control chemical and microbiological testing of Finished Product, Raw Materials, and Packaging components, as well as oversight over maintenance for quality control instrumentation in accordance with cGMP/FDA regulations, internal standard operating procedures, and policies. This role also includes people leadership responsibilities for one shift in the QC operations group. Due to the nature of the radioactive process, this role requires proficiency of quality control techniques, analytical instrumentation, sterility principles, and an understanding of radiation safety standards.Shift: Wednesday - Saturday PM (3 pm to 1 am) Location: Millburn, NJ #LI-Onsite This role is located on-site in Millburn, NJ. Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you. Job Description Key Responsibilities: Demonstrates unbossed behavior, leading analysts and senior analysts in the QC lab through technical aspects related to quality control testing readiness, including QC reagents and materials management, equipment preparation / daily cleaning and maintenance activities, sample management and QC testing, and documentation completion / review in full compliance with GMP regulations, internal procedures, and product specifications.
Essential Requirements
Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between $85,400 and $158,600/year; however, while salary ranges are effective from 1/1/25 through 12/31/25, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills, and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an "at-will position" and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. 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. Accessibility and reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Salary Range $85,400.00 - $158,600.00Skills Desired Continued Learning, Dealing With Ambiguity, Decision Making Skills, Gxp, Industry Standards, Laboratory Equipment, Laboratory Excellence, Quality Control (Qc) Testing, Quality Control Sampling, Self-Awareness, Technological Expertise, Total Quality Management |