Quality Control Specialist II

U473 (FCRS = US473) Novartis Innovative Technologies Inc; Morrisville (NC); On-site; USD 90,000 - 166,000; Full time

Job summary

Novartis Innovative Technologies Inc in Morrisville, NC seeks a QC Specialist II to support a growing Small Molecules Quality Control lab. You will act as SME for analytical methods, lead transfers and validations, and collaborate across QA/QC, MS&T, Engineering, and Validation.

The role requires hands-on experience with HPLC/UPLC/GC/LC-MS, data review, and ensuring GxP compliance. Strong training and leadership skills are a plus in a GMP environment.

Qualifications

• Bachelor's, Master's, or PhD in Chemistry or related field with cGMP experience.
• Hands-on with HPLC/GC/UPLC/LC-MS and method validation/transfer.
• Experience with LabWare LIMS and Empower CDS preferred.

Responsibilities

• Serve as SME for complex analytical techniques and instrumentation.
• Perform and troubleshoot testing of materials and products per GLP/cGMP.
• Lead method transfers, validation, troubleshooting, and lifecycle management.
• Investigate OOS and deviations with root-cause analysis and CAPA.
• Review data and tests for readiness of analytical release.
• Support equipment qualification and calibration; provide training.

Skills

HPLC

UPLC

GC

LC-MS

ICP spectroscopy

Dissolution

Spectroscopy

Physicochemical testing

GxP

ALCOA+ data integrity

Education

Bachelor's, Master's, or PhD in Chemistry/Analytical Chemistry/Pharmaceutical Sciences

Tools

LabWare LIMS

Empower CDS

Job description

Job Description Summary

Location: Morrisville, North Carolina The QC Specialist II is a highly skilled laboratory professional who will support the start-up and growth of Novartis' Small Molecules Quality Control laboratory in Morrisville, North Carolina. This role serves as a technical subject matter expert for complex analytical techniques and instrumentation while supporting analytical testing, investigations, method transfer, validation, and data review activities within a GMP-regulated environment. Working within a growing site organization, the QC Specialist II will support the transfer, qualification, validation, and lifecycle management of analytical methods used to test pharmaceutical raw materials, in-process materials, finished products, and stability samples. The role will also provide technical leadership in troubleshooting, analytical investigations, equipment qualification, and training activities while partnering across Quality, Manufacturing, MS&T, Engineering, and Validation teams. This is an exciting opportunity to help build the technical capabilities, laboratory systems, and quality infrastructure required to support the continued growth of the Morrisville manufacturing site.

Job Description Key Responsibilities

• Serve as a subject matter expert for complex analytical techniques and instrumentation, including HPLC, UPLC, GC, LC-MS, ICP spectroscopy, dissolution, spectroscopy, and physicochemical testing.
• Perform and troubleshoot chromatographic and wet-chemistry testing of raw materials, in-process materials, finished products, and stability samples in compliance with GLP and cGMP requirements.
• Manage analytical method transfers, validation, troubleshooting, risk mitigation, and lifecycle-management activities to support the Morrisville Quality Control laboratory.
• Lead and support OOS and deviation investigations, including root-cause analysis, CAPA definition, issue resolution, and KPI/KQI trending.
• Review and approve chromatographic and non-chromatographic data and analytical tests, ensuring data integrity, accuracy, and readiness for analytical release.
• Provide expert support for laboratory equipment and system qualification and validation, including user requirements specifications, functional specifications, IQ/OQ/PQ activities, calibration, maintenance, and qualification-plan preparation.
• Develop and deliver site training for Empower CDS, complex analytical technologies, laboratory processes, and applicable quality requirements.
• Ensure activities comply with GxP, ALCOA+ data-integrity principles, regulatory requirements, and Novartis policies while collaborating across QA, QC, MS&T, Engineering, Operations, and other site functions.

Essential Requirements

Bachelor's, Master's, or PhD in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline, with working experience in technical drug development, manufacturing, analytics, or quality within a cGMP-regulated environment. Hands-on experience with HPLC, GC, UPLC, and/or LC-MS analysis, including experience with analytical method validation and transfer; experience with LabWare LIMS and Empower CDS is preferred. Proven experience in analytical method development, validation, transfer, troubleshooting, and lifecycle management. Strong technical knowledge of complex analytical techniques, such as HPLC, UPLC, GC, ICP, dissolution, LC-MS, spectroscopy, and physicochemical testing. Good understanding of GxP, ALCOA+ data-integrity principles, ICH Q2, ICH Q10, ICH Q14, and relevant FDA, EMA, and other regulatory expectations. Broad knowledge of cGMP requirements and experience working within technical drug development, manufacturing, analytical, or quality operations.

Desirable Requirement

Prior experience developing and delivering technical training related to analytical instrumentation, laboratory systems, or quality control processes.

Salary

The salary for this position is expected to range between $89,600 - $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.

Skills Desired

Analytical Testing, Collaboration, Communication, Data Integrity, Decision Making, Good Manufacturing Practices (GMP), Managing Ambiguity, Quality Assurance (QA), Quality Compliance, Quality Control (QC), Quality Management Systems (QMS), Regulatory Compliance, Standard Operating Procedure (SOP), Statistical Process Control (SPC), Validation Activities

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s 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.

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 [e-mail] or call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range $89,600.00 - $166,400.00