Expert Science & Technology, Quality Control (2nd shift Tuesday-Friday)

Band

Level 3

Job Description Summary

Internal Title: Expert Science & Technology
This position will be located at the East Hanover NJ site and will not have the ability to be located remotely. Please note that this role would not provide relocation and only local candidates will be considered.

This is a shift position. The shift for this role will be Tues- Friday and weekend coverage as needed 10 hour shift 10am -8pm. Shift will be fixed according to business need

Novartis expands its early development and innovative CAR-T cell therapy manufacturing capabilities in its newly launched Center of Excellence located in the East Hanover NJ campus. Our therapies are being developed as transformative treatments with life-saving potential for various B cell malignancies and other oncological diseases. We look to be bold with purpose as we reimagine medicine and lead the way in advancing scientific breakthroughs for patients.

The Expert Science & Technology will be assigned operational activities within the remit of the department such as clinical program support patient safety or OpEx. Individually contribute to and support all GxP activities in the department. Administers Quality Systems and processes (including documentation metrics and monitoring of actions). Supports establishment of Quality operational processes. Performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards. Supports Quality Projects and initiatives. Learn and grow into the next role. Under general direction perform bioanalytical testing and other activities in functions supporting the Quality Control department.

Job Description

Key responsibilities include but are not limited to:

• **Shift position**Shift: Tues- Friday and weekend coverage as needed 10 hour shift 10am -8pm. Shift will be fixed according to business need.

• Perform bioanalytical testing and support activities compliantly following appropriate SOPs and procedures.

• Peer review and archive analytical data in lab documentation systems.

• Draft finalize and revise technical protocols procedures and reports with minimal supervision.

• Support execution of method qualification/development & optimization/transfer as governed by protocols and/or under the supervision.

• Train other associates in specific areas of competency.

• Lead and/or contribute to writing CAPAs/OOS/OOE/OOT and perform deviation investigations.

• Support change control as required.

• Support 5S and Lean projects.

• Knowledge of LabWare LIMS and/or other QC data systems.

• Knowledge of appropriate GMP/GLP quality systems (ESOPs Trackwise BMRAM etc.).

• Interface with regulatory agencies during audits as required.

• In addition to these primary duties provide coverage for all appropriate areas.

Minimum Requirements:

• Bachelors degree is required. A degree in science is preferred. Advanced degree may be an advantage but not essential.

• Minimum 3 years of experience in the pharmaceutical biologics Biotechnology or medical device industry ideally in a QC laboratory setting.

• Thorough knowledge of bioassay test methods (Elisa flow cytometry qPCR cell culture) is required.

• Strong written and verbal communication skills are essential.

• Experienced in the use of computer -based systems and applications.

Desired Requirements:

• Good understanding of the concepts of cGxP and knowledge of ICH Eur. Ph. USP and FDA and JP guidelines is preferred.

• Experience in support/writing OOS/OOE/OOT and/or deviation investigations and knowledge of CAPA is preferred.

Novartis Compensation and Benefit Summary: The pay range for this position at commencement of employment is expected to be between: $77000-$143000/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 gender national origin age sexual orientation gender identity or expression marital or veteran status disability or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

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 in order to perform the essential functions of a position please send an e-mail to call 1 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Range

$77000.00 - $143000.00

Skills Desired

Agility Audit Management Business Partnering Change Control Continued Learning Health Authorities Influencing Skills Knowledge Of Capa Qa (Quality Assurance) Quality Management Quality Management Systems (QMS) Risk Management Root Cause Analysis (RCA) Self-Awareness Sop (Standard Operating Procedure) Technological Expertise