Top 27 Quality manager Jobs in Mebane Nc

Head, QA Ops and Compliance (Associate Director Level)
Novartis —Durham, NC
- $138,600 - $257,400 a year
- Full-time
- Bachelor of Science
- English
- Bachelor's degree
- Health insurance
- 401(k) matching
Manager Quality
Dauch —Mebane, NC
- Full-time
- 5 years
- Engineering
- In-person
Technical Manager, NA
IPS Corporation —Durham, NC
- Overtime
- Microsoft Office
- 8 years
- Presentation skills
Quick Apply
Director, Quality Assurance - Regulatory
Labcorp —Burlington, NC
- $130,000 - $150,000 a year
- Full-time
- 3 years
- Fair chance
- Senior level
- Employee stock purchase plan
- Disability insurance
Quality Control Manager
Berkshire Corporation —Whitsett, NC
- Full-time
- Analysis skills
- Math
- Mentoring
- Paid holidays
- Disability insurance
Quick Apply
Parts Quality Mass Production Group Lead
Honda —Haw River, NC
- $90,200 - $112,700 a year
- Overtime
- 5 years
- Engineering
- Data analysis skills
- Paid holidays
- Loan repayment program
Quality Manager
Micross Advanced Interconnect Technology —Durham, NC
- Bachelor of Science
- Engineering
- ERP systems
- Health savings account
- Paid holidays
Quick Apply
Director, Data Quality
IQVIA —Burlington, NC
- $110,200 - $307,200 a year
- Full-time
- Computer Science
- 5 years
- Office
13d
Quality Assurance Manager (Onsite)
Voltage LLC —Chapel Hill, NC
- Full-time
- 5 years
- Engineering
- Analysis skills
Quick Apply
Quality Director
AMETEK, Inc. —Whitsett, NC
- $135,000 - $185,000 a year
- Engineering
- Master's degree
- Travel
Quality Manager (Regulated Industry)
Mentor Technical Group —Durham, NC
- Full-time
- Spanish
- Microsoft Outlook
- 5 years
Test Lead – Facets (Medicare/Medicaid)
Cognizant —Durham, NC
- $93,000 - $109,000 a year
- Full-time
- Hybrid work
- 8 years
- SQL
- Analysis skills
- Paid parental leave
- Employee stock purchase plan
6d
Lead Technician, Quality Control - 1st Shift - $32.20/hr
Stryker —Durham, NC
- $32.20 an hour
- Full-time
- 5 years
- High school diploma or GED
- Continuous improvement
- Health savings account
- AD&D insurance
Supervisor, Accounts Receivable - CSA QA and Ambulatory Support - Hybrid
Duke Health —Durham, NC
- Full-time
- Hybrid work
- Mid-level
- Analysis skills
- Associate's degree
Director of Data Quality and Evaluation
Communities In Schools North Carolina —Durham, NC
- Full-time
- Hybrid work
- School experience
- Computer literacy
- Writing skills
Quick Apply
Quality Mart Manager
Quality Mart by Quality Oil Company —Liberty, NC
- $38,000 - $42,000 a year
- Weekends as needed
- Background check
- Mid-level
- Team management
- Health insurance
- Dental insurance
Quick Apply
6h
Quality Plus Store Manager
Quality Plus/GOGAS by Quality Oil Company LLC —Durham, NC
- $38,000 - $42,000 a year
- Weekends as needed
- Background check
- Customer service
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
6h
Quality Assurance Supervisor
Voltage LLC —Timberlake, NC
- Full-time
- Microsoft Excel
- Ability to walk for extended periods
- Engineering
Quick Apply
7d
Contractor Quality Assurance/Control Supervisor - Landfill Construction/Cap Construction
Ayuda Companies —United States
- $90,000 - $120,000 a year
- Full-time
- Background check
- Construction site
- Pass drug screening
- Disability insurance
- Health insurance
Quick Apply
Construction Quality Control Manager- USACE
Thalle Construction Company —United States
- Full-time
- Construction site
- In-person
- Senior level
- Paid holidays
- Disability insurance
Quick Apply

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quality manager jobs near mebane nc

Head, QA Ops and Compliance (Associate Director Level)

Novartis -
Durham, NC

Apply Now

Job Details

Full-time
$138,600 - $257,400 a year

Benefits

Health insurance
401(k) matching

Qualifications

Incident investigation techniques for hazard identification
Regulatory inspections
Investigations regulatory compliance
Team leadership
Operational management
Preventive action implementation
Production deviation management
Quality control preventive actions
Corrective and preventive actions (CAPA)
English
GMP
Internal investigations
Quality control audit
Team development
Production validation processes
Pharmaceutical company experience
Technology transfer (scale-up process)
Quality assurance experience within pharmaceutical industry
Collaboration with manufacturing teams
Quality control experience within pharmaceutical industry
Operational excellence initiatives
Quality audits
Managing product quality assurance teams
Cross-functional communication
Audit support
Pharmaceutical manufacturing facility experience

Full Job Description

Summary

The Head, QA Ops and Compliance (Associate Director Level) provides strategic and hands on leadership for Quality Assurance within the Small Molecule Operations division, ensuring excellence in cGMP compliance, regulatory execution, and quality oversight across all operational activities. This role leads and develops Quality Assurance Managers, partners closely with manufacturing and external suppliers, and ensures that all products, manufactured on site, by external partners, or imported, are released to market in full alignment with Novartis Quality Standards, policies, and global regulatory requirements. The Head, QA Ops and Compliance plays a pivotal role in safeguarding product quality, enabling operational excellence, and supporting the reliable and compliant supply of high quality small molecule therapies to patients.

About the Role

#LI-Onsite

Location: Durham, NC

This role is on-site 5 days a week and does not have the ability to work remotely. This role is located in Durham, NC and will eventually move to Morrisville, NC at a later date

Role scope, level, and compensation are set at the Associate Director level; Director‑level appointment is not within scope for this position.

Key Responsibilities:

Provide end-to-end leadership for Quality Operations and Compliance across manufacturing, Quality Control, AS&T, and logistics, ensuring adherence to cGMP, regulatory requirements, and internal quality standards.
Serve as the final QA authority for review, approval, and release of batch documentation and patient or commercial product lots manufactured at the site.
Ensure strong on-the-floor QA presence, delivering real-time quality oversight, decision-making, and guidance to support compliant and efficient operations.
Lead investigations of deviations, OOX/OOS events, complaints, and adverse events, ensuring timely root cause analysis, effective CAPA implementation, and sustainable corrective actions.
Implement and maintain site Quality Systems, including SOP governance, training compliance, documentation control, and inspection readiness for internal, external, and regulatory audits.
Drive QA Operational Excellence through performance metrics (KPIs/KQIs), continuous improvement initiatives, and proactive identification of quality and process risks.
Provide QA leadership for technology transfers, process validation, and new equipment commissioning, including review and approval of validation strategies and OQ/PQ execution.
Lead, develop, and retain a high-performing QA team through hiring, coaching, performance management, and resource planning, while supporting budget and capacity planning in alignment with site strategy.

Essential Requirements:

BS or MS in Life Sciences, Pharmacy, Chemistry, Biotechnology, or related scientific discipline; advanced degree preferred.
Minimum 10+ years of experience in pharmaceutical, biotechnology, or cell and gene therapy industry within cGMP regulated environments.
Demonstrated experience supporting Small Molecule Operations (SMO), including small molecule drug product and/or drug substance environments.
Demonstrated hands-on leadership in Quality Operations and Quality Systems & Compliance, with direct responsibility for product release, quality systems, and audit readiness within Small Molecule Operations (SMO).
Minimum 6-10 years of direct people leadership, including team development, performance management, and cross-functional collaboration.
Strong working knowledge of FDA, EMA, and global regulatory requirements, including experience supporting regulatory inspections and audits.
Proven experience leading deviation investigations, CAPA management, and continuous improvement initiatives in an operational QA setting.
Experience supporting manufacturing operations, Quality Control, validation, and technology transfer activities.
Excellent communication, decision-making, and organizational skills, with the ability to operate effectively in a fast-paced CGT manufacturing environment.
Fluency in English (written and verbal).

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $138,600 and $257,400/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.

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? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

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 e-mail to [email protected] 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.

Division

Operations

Business Unit

Production / Manufacturing

Location

USA

State

North Carolina

Site

Durham

Company / Legal Entity

U473 (FCRS = US473) Novartis Gene Therapies

Functional Area

Quality

Job Type

Full time

Employment Type

Regular

Shift Work

Apply Now

Refine Your Search

quality manager jobs in mebane nc

Head, QA Ops and Compliance (Associate Director Level)

Manager Quality

Technical Manager, NA

Director, Quality Assurance - Regulatory

Quality Control Manager

Parts Quality Mass Production Group Lead

Quality Manager

Director, Data Quality

Quality Assurance Manager (Onsite)

Quality Director

Quality Manager (Regulated Industry)

Test Lead – Facets (Medicare/Medicaid)

Lead Technician, Quality Control - 1st Shift - $32.20/hr

Supervisor, Accounts Receivable - CSA QA and Ambulatory Support - Hybrid

Director of Data Quality and Evaluation

Quality Mart Manager

Quality Plus Store Manager

Quality Assurance Supervisor

Contractor Quality Assurance/Control Supervisor - Landfill Construction/Cap Construction

Construction Quality Control Manager- USACE

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