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Novartis Engineering Jobs in Raleigh, NC (NOW HIRING)

Principal Engineer, MS&T

Durham, NC · On-site

$126K - $234K/yr

Novartis is unable to offer relocation support for this role: please only apply if this location is ... Partner cross-functionally with Manufacturing, Quality, Engineering, and Validation teams to ensure ...

Senior Engineer, Automation

Durham, NC · On-site

$108.50 - $201.50/hr

Novartis does not offer relocation support. Key Responsibilities * Ensure automation aspects of new ... S. degree in Engineering, Computer Science, or a related technical field. * 8 years of experience ...

Senior Project Manager

Durham, NC · On-site

$108K - $201K/yr

Working across Engineering, Construction, Manufacturing, Quality, Automation, EHS, and external ... Novartis is unable to offer relocation support for this role: please only apply if this location is ...

IT/OT Lab Specialist

Durham, NC · On-site

$98K - $183K/yr

As an IT/OT Lab Specialist at Novartis, you will play a key role in supporting the computerized ... Essential Requirements: * Bachelor's degree in Engineering, Computer Science, Information ...

Novartis is unable to offer relocation support for this role: please only apply if this location is ... Bachelor's biochemistry, chemical engineering, bioengineering, or related technical field with 4-6 ...

Showing results 21-40

Novartis Engineering information

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How much do novartis engineering jobs pay per hour?

As of Sep 3, 2026, the average hourly pay for novartis engineering in Raleigh, NC is $30.67, according to ZipRecruiter salary data. Most workers in this role earn between $19.62 and $36.92 per hour, depending on experience, location, and employer.

What is Novartis Engineering?

Novartis Engineering refers to the specialized teams and professionals at Novartis, a global pharmaceutical company, who are responsible for designing, developing, maintaining, and optimizing manufacturing processes, facilities, and equipment. These engineers play a crucial role in ensuring that pharmaceutical products are produced efficiently, safely, and in compliance with regulatory standards. Their work includes process engineering, automation, facility projects, and continuous improvement initiatives to support innovative drug development and production.

What are the key skills and qualifications needed to thrive as a Novartis engineer?

To thrive as a Novartis Engineer, you need a strong background in engineering principles—such as process, chemical, or mechanical engineering—typically supported by a relevant degree and industry experience in pharmaceuticals or life sciences. Familiarity with systems like Good Manufacturing Practice (GMP), Computerized Maintenance Management Systems (CMMS), and validation protocols, as well as certifications like Six Sigma or Lean, is commonly required. Strong problem-solving, teamwork, and communication skills help engineers excel in cross-functional, regulated environments. These competencies ensure that engineering projects meet high standards for quality, compliance, and operational efficiency within the pharmaceutical sector.

How does a Novartis engineer typically collaborate with cross-functional teams to drive innovative solutions in pharmaceutical manufacturing?

Engineers at Novartis frequently work in multidisciplinary teams alongside scientists, quality assurance specialists, production staff, and IT professionals to optimize manufacturing processes and implement new technologies. Collaboration often involves participating in project meetings, sharing technical expertise, and jointly troubleshooting complex production issues. This teamwork-driven environment not only fosters innovation but also ensures compliance with strict regulatory standards. Effective communication and a proactive approach to problem-solving are essential for success in this dynamic and impactful role.

What is the difference between Novartis Engineering vs Novartis Quality Assurance?

AspectNovartis EngineeringNovartis Quality Assurance
Required CredentialsBachelor's in Engineering or related field, technical certificationsBachelor's in Life Sciences, Quality Management certifications
Work EnvironmentManufacturing plants, R&D labs, technical departmentsQuality labs, compliance departments, manufacturing oversight
Employer & Industry UsageDesign, maintain, and improve manufacturing processesEnsure product quality, compliance, and regulatory standards

Novartis Engineering focuses on designing and maintaining manufacturing processes, requiring engineering credentials. In contrast, Novartis Quality Assurance emphasizes product quality and compliance, often requiring quality management certifications. Both roles are essential in pharmaceutical production but serve different functions within the same industry.

What are popular job titles related to Novartis Engineering jobs in Raleigh, NC?

For Novartis Engineering jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Novartis Engineering jobs in Raleigh, NC look for?

The top searched job categories for Novartis Engineering jobs in Raleigh, NC are:

Infographic showing various Novartis Engineering job openings in Raleigh, NC as of August 2026, with employment types broken down into 92% Full Time, 4% Part Time, 3% Contract, and 1% Nights. Highlights an 84% Physical, 4% Hybrid, and 12% Remote job distribution, with an average salary of $63,792 per year, or $30.7 per hour.

Sr. Engineer, MS&T - Aseptic Drug Product

Novartis Group Companies

Durham, NC • On-site

$114K - $211K/yr

Other

Medical, Life, Retirement, PTO

Posted 12 days ago


Job description

Job Description Summary

Imagine being at the forefront of delivering life-changing sterile medicines to patients around the world. As Sr. Engineer, Manufacturing Science and Technology - Aseptic Drug Product, you will play a critical role in advancing aseptic manufacturing operations by providing technical leadership, driving process performance, and supporting the successful introduction of new products and technologies. Working closely with Manufacturing, Quality, Engineering, and global partners, you will help solve complex challenges, lead continuous improvement initiatives, and ensure a reliable supply of high-quality products for patients. This is an exciting opportunity to make a meaningful impact in a collaborative environment that values innovation, scientific excellence, and operational excellence.


Job Description

Location:

  • This position will be located in Durham, NC and will be an onsite role.
  • Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

  • Lead CPV activities by analyzing process data, identifying trends, and driving process performance improvements.
  • Serve as the MS&T technical lead for manufacturing investigations, root cause analysis, and issue resolution.
  • Partner with Manufacturing to support production schedules, commercial supply, and compliance with GMP requirements.
  • Monitor and trend CQAs and CPPs to ensure consistent product quality and process control.
  • Identify, evaluate, and implement process improvements that enhance reliability, efficiency, and performance.
  • Support the introduction of new equipment, systems, and manufacturing processes through startup and implementation activities.
  • Author and support process change documentation while collaborating with Engineering, Manufacturing, and Validation teams.
  • Provide technical expertise for remediation efforts, project deliverables, technical assessments, and process reports.
  • Collaborate with Development and site partners to execute Tech Transfer activities and ensure successful product commercialization.
  • Drive OPEX initiatives and foster a culture of continuous improvement, quality, and manufacturing excellence.

Essential Requirements:

  • Bachelor's degree in Biochemistry, Chemical Engineering, Bioengineering, or a related technical field with 6+ years of biopharmaceutical manufacturing experience; Master's degree with 4+ years of experience; or Doctorate degree with 2+ years of experience.
  • Proven experience supporting GMP biopharmaceutical manufacturing operations within a regulated environment.
  • Hands-on experience with aseptic fill-finish operations and sterile drug product manufacturing.
  • Experience supporting Tech Transfer, process validation, lifecycle management, or manufacturing process improvements.
  • Working knowledge of global GMP regulations, validation requirements, and quality compliance expectations.
  • Strong analytical skills with the ability to interpret process data, identify trends, and drive data-based decisions.
  • Excellent technical writing, communication, and cross-functional collaboration skills.
  • Demonstrated ability to lead technical initiatives and contribute effectively within cross-functional teams.

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $114,100 and $211,900 annually

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.

#LI-Onsite


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

$114,100.00 - $211,900.00


Skills Desired

Applied Statistics, Manufacturing Production, Manufacturing Technologies, Operational Excellence, Process Control, Quality Compliance, Regulatory Compliance, Technical Leadership, Technology Transfer