About this role
Novartis QC Specialist II – LIMS/Master Data
Location: Morrisville, North Carolina
Relocation Support: This role is based in Morrisville, North Carolina. Novartis is unable to offer relocation support: please only apply if accessible.
At Novartis, quality data drives the delivery of medicines that patients depend on every day. As a QC Specialist II – LIMS/Master Data, you will play a critical role in building, maintaining, and optimizing LabWare LIMS that supports Quality Control operations. This is an exciting opportunity to combine your scientific background, technical expertise, and problem-solving skills to influence data integrity, laboratory efficiency, and compliance across a growing manufacturing environment while helping ensure the highest standards of product quality.
Essential Requirements
- Bachelor’s degree in Chemistry, Biology, or a related scientific discipline.
- LIMS master data experience is required, including foundational experience with LabWare LIMS
- Understanding of structures and data flow requirements in LIMS systems.
- Empower Master Data and method building experience is required.
- Experience implementing instrument connections, Environmental Monitoring test plans, test scheduling and LES implementations
- Knowledge of International Council for Harmonisation Q10 principles, data integrity requirements, change control, and Good Documentation Practices.
- Strong communication skills with the ability to identify, prioritize, and escalate issues in a dynamic environment.
Desirable Requirements
- At least 1 year of GMP laboratory and system infrastructure experience
- Applied working knowledge of various laboratory instrumentation.
The salary for this position is expected to range between $89,600 and $166,400 per year. The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors. Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards. US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.
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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 & 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 inquiry and let us know the nature of your request and your contact information. Please include the job requisition number in your message.
Division
Operations
Business Unit
Production / Manufacturing
Location
USA
State
North Carolina
Site
Morrisville
Company / Legal Entity
U473 (FCRS = US473) Novartis Innovative Technologies Inc
Functional Area
Quality
Job Type
Full time
Employment Type
Regular
Shift Work
No
Job ID
REQ-10087939