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Novartis Engineering Jobs (NOW HIRING)

Novartis is unable to offer relocation support for this role: please only apply if this location is ... S. degree in Engineering, Computer Science, or related technical field. * 8 years work experience ...

Validation Lead

Indianapolis, IN · On-site

$114K - $211K/yr

You'll partner closely with Manufacturing Science and Technology, Engineering, Information ... Novartis may change the published salary range based on company and market factors. Your ...

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 ...

Validation Lead

Indianapolis, IN · On-site

$114K - $211K/yr

You'll partner closely with Manufacturing Science and Technology, Engineering, Information ... Novartis may change the published salary range based on company and market factors. Your ...

Novartis is unable to offer relocation support for this role: please only apply if this location is ... Implement process improvements in collaboration with operations and engineering teams * Support ...

Strong communication and collaboration skills when working across engineering, quality, and operations teams Novartis Compensation and Benefit Summary: The salary for this position is expected to ...

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Novartis Engineering information

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$12

$31

$57

How much do novartis engineering jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for novartis engineering in the United States is $31.55, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $37.98 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Novartis Engineer, and why are they important?

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 an engineer at Novartis 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 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 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.

More about Novartis Engineering jobs
What cities are hiring for Novartis Engineering jobs? Cities with the most Novartis Engineering job openings:
What states have the most Novartis Engineering jobs? States with the most job openings for Novartis Engineering jobs include:
What job categories do people searching Novartis Engineering jobs look for? The top searched job categories for Novartis Engineering jobs are:
Infographic showing various Novartis Engineering job openings in the United States as of May 2026, with employment types broken down into 94% Full Time, 4% Part Time, and 2% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $65,624 per year, or $31.6 per hour.

Senior Engineer, Automation

Novartis

Durham, NC

$108K - $201K/yr

Full-time

Medical, Life, Retirement, PTO

Posted 4 days ago


Novartis rating

7.4

Company rating: 7.4 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

53rd of 71 rated pharmaceutical


Job description

Job Description Summary

The Senior Automation Engineer reports to the AD Process Automation and is responsible for providing automation design team leadership and serving as a technical subject matter expert for a Novartis Aseptic Drug Product facility.


Job Description

Location: This position will be located in Durham, NC and will be an On-Site role.

Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Key Responsibilities:

  • Ensure automation aspects of new equipment are appropriately designed, meet Novartis standards and are appropriately commissioned and qualified.
  • Provide oversight for automation aspects of projects including integration of 3rd party equipment to other standard plant systems, e.g., DCS, BMS, Historian, Infrastructure.
  • Provide design, configuration, installation, and maintenance of automation software and associated hardware for existing equipment and processes.
  • Prepare scopes of work for large projects, lead small teams and manage automation contractors as required to complete required work within project timelines.
  • Lead discussions with internal business partners on priorities, timelines and transparent sharing of information.
  • Develop, review and approve lifecycle documentation, e.g., User Requirements (URS), Functional Specification (FS) and Detail Design Specifications (DDS/HDS/SDS).
  • Develop and maintain procedures to meet GMP requirements, CFR's and internal company policies.
  • Participate and/or lead new product implementation processes to ensure smooth transition from process development into GMP manufacturing.
  • Drive operational excellence and continuous improvement.
  • Partner with Quality to ensure a quality and compliant manufacturing environment including participation in regulatory audits as an automation SME.
  • Solve technical related issues impacting production.
  • Support 24x7 site-based operations including rotating on-call responsibilities.
  • Support investigations of non-conformances related to automation systems.
  • Other related duties as assigned.

Essential Requirements:

  • B.S. degree in Engineering, Computer Science, or related technical field.
  • 8 years work experience in pharmaceutical or biopharmaceutical based GMP manufacturing operations, or equivalent work experience (12 years) in pharmaceutical or biopharmaceutical based GMP manufacturing operations.
  • Excellent oral and written communication skills, including demonstrated technical writing skills.
  • Experience programming, troubleshooting, and maintaining various site automation systems including DCS, BMS, PLC, SCADA, historian, infrastructure, including use of various industrial protocols.
  • Experience in development and execution of system level qualification testing including providing guidance on qualification plans in conjunction with C&Q department.
  • Proven experience applying S88 in an automated environment and development of control system standards aligning with S88 methodology.
  • Experience in field wiring practices and panel design, experience with troubleshooting and start-up of control systems, and experience with instrumentation.
  • Experience writing and executing complex change controls.
  • In-depth knowledge of FDA regulations particularly 21 CFR part 11 and GMP systems.
  • Strong project management skill set with extensive experience in strategic / tactical planning, demonstrated ability to perform long-term project planning.
  • Ability to prepare contingency plans and logically work through complex issues in a pressure filled atmosphere.
  • Provide technical support on all manufacturing issues when driving towards issue resolution.
  • Up to 10% travel may be required.

Novartis Compensation and Benefit Summary:

The salary for this position is expected to range between $108,500 and $201,500 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

$108,500.00 - $201,500.00


Skills Desired

Api (Application Programming Interface), Api (Application Programming Interface), Automation, Back-End Development, Business Continuity, Change Control, Chemistry, Design Development, Electronic Components, General Hse Knowledge, Including Gdp, Java (Programming Language), Knowledge Of Capa, Knowledge Of Gmp, Kubernetes, Managing Performance Improvement, Manufacturing Production, Mathematical Optimization, Project Commissioning, Project Engineering, Project Execution, Reactjs, Risk Management, Root Cause Analysis (RCA), Scheduler {+ 2 more}