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Manufacturing Process Engineer Jobs in Raleigh, NC

Novartis

Process Engineer III

Durham, NC

$98K - $183K/yr

Summary Step into a pivotal engineering role where your expertise directly shapes advanced manufacturing operations. As a Process Engineer III, you will support the design, validation, maintenance ...

Micross

Process Engineer

Durham, NC · On-site

... manufactured to the highest quality standards. Over the years, Micross Components acquired the ... Summary: We are seeking a knowledgeable, self-motivated engineer for our growing process ...

AskBio

Process Engineer II

Durham, NC · On-site

Position Summary AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer II to join our Process Engineering team and support current and future commercialization efforts.

DivIHN

Process Engineer Pharmaceuticals I

NC · On-site

Process Engineer Pharmaceuticals I Duration: 7+ Months Location: Research Triangle Park, NC Only W2 ... This role is execution-focused, supporting upstream and downstream manufacturing operations ...

AskBio

Process Engineer II

Durham, NC

Position Summary AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer II to join our Process Engineering team and support current and future commercialization efforts.

Forge Nano

Director of Process Engineering

Raleigh, NC · On-site

Lead and manage the battery manufacturing process * Create a process engineering vision, develop a strategy, and hold teams accountable to deliver high-impact business results (KPIs). * Implement ...

Forge Nano

Director of Process Engineering

Raleigh, NC · On-site

Lead and manage the battery manufacturing process * Create a process engineering vision, develop a strategy, and hold teams accountable to deliver high-impact business results (KPIs). * Implement ...

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All JobsManufacturing Process Engineer JobsManufacturing Process Engineer Jobs in Raleigh, NC

Manufacturing Process Engineer information

See Raleigh, NC salary details

$49.1K

$85.7K

$123.5K

How much do manufacturing process engineer jobs pay per year?

As of Jun 11, 2026, the average yearly pay for manufacturing process engineer in Raleigh, NC is $85,731.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,400.00 and $95,300.00 per year, depending on experience, location, and employer.

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

To thrive as a Manufacturing Process Engineer, you need a solid background in engineering principles, process optimization, and quality control, usually supported by a degree in mechanical, industrial, or manufacturing engineering. Familiarity with CAD software, statistical process control (SPC) tools, Lean/Six Sigma methodologies, and enterprise resource planning (ERP) systems is typically required. Strong problem-solving abilities, analytical thinking, and effective communication skills help distinguish top performers in this role. These skills and qualifications are crucial for improving efficiency, ensuring product quality, and driving continuous improvement in manufacturing operations.

What engineer makes $500,000 a year?

While most manufacturing process engineers earn less than $200,000 annually, some senior or specialized engineers with extensive experience, advanced skills, or leadership roles can reach or exceed $500,000 a year, especially in high-cost-of-living areas or large corporations. Achieving this level often requires advanced certifications, significant responsibility, and a track record of impactful results.

What are some common challenges faced by Manufacturing Process Engineers in optimizing production lines?

Manufacturing Process Engineers often encounter challenges such as balancing efficiency with product quality, integrating new technologies without disrupting ongoing operations, and troubleshooting bottlenecks in the production line. They must work closely with cross-functional teams—including quality assurance, maintenance, and operations—to identify root causes of inefficiencies and implement sustainable solutions. Adapting to evolving industry standards and continuous improvement initiatives is also a key part of the role, requiring flexibility and strong problem-solving skills.

What engineers make $300,000 a year?

Senior manufacturing process engineers with extensive experience, advanced skills in automation and process optimization, and often specialized certifications can earn salaries approaching or exceeding $300,000 annually. High-level roles in industries such as aerospace, semiconductor manufacturing, or oil and gas tend to offer these compensation levels, especially with leadership responsibilities and significant project management duties.

What is the difference between Manufacturing Process Engineer vs Manufacturing Engineer?

AspectManufacturing Process EngineerManufacturing Engineer
Primary FocusDesigning, analyzing, and improving manufacturing processesOverseeing overall manufacturing operations and production workflows
Typical ResponsibilitiesProcess optimization, troubleshooting, implementing new technologiesProduction planning, equipment management, quality control
CredentialsBachelor's in engineering, certifications like Six Sigma often preferredBachelor's in engineering or manufacturing, similar certifications
Work EnvironmentFactories, labs, process development settingsFactories, production lines, plant management

While both roles require engineering backgrounds and similar certifications, Manufacturing Process Engineers focus on refining manufacturing processes, whereas Manufacturing Engineers oversee the entire production process. Understanding these distinctions helps in choosing the right career path or job search focus.

What does a process manufacturing engineer do?

A process manufacturing engineer designs, develops, and optimizes manufacturing processes to improve efficiency, quality, and safety. They analyze production workflows, troubleshoot issues, and implement process improvements using tools like Six Sigma and CAD software. The role often requires knowledge of automation, quality standards, and continuous improvement methodologies.

Are process engineers paid well?

Process engineers typically earn competitive salaries that vary based on experience, location, and industry. They often receive additional benefits such as bonuses and professional development opportunities, reflecting the technical skills and problem-solving expertise required for the role.

What does a Manufacturing Process Engineer do?

A Manufacturing Process Engineer is responsible for designing, implementing, and optimizing manufacturing processes within a production facility. Their main goal is to improve efficiency, reduce costs, and ensure product quality by analyzing workflows, selecting appropriate equipment, and troubleshooting production issues. They often collaborate with other engineers, quality assurance teams, and production staff to develop and refine processes. This role may also involve implementing automation, maintaining safety standards, and supporting continuous improvement initiatives.
What are the most commonly searched types of Manufacturing Process Engineer jobs in Raleigh, NC? The most popular types of Manufacturing Process Engineer jobs in Raleigh, NC are:
What are popular job titles related to Manufacturing Process Engineer jobs in Raleigh, NC? For Manufacturing Process Engineer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Manufacturing Process Engineer jobs in Raleigh, NC look for? The top searched job categories for Manufacturing Process Engineer jobs in Raleigh, NC are:
Manufacturing Process Engineer jobs near you
Process Engineer II

Process Engineer II

Asklepios BioPharmaceutical, Inc.

Durham, NC • On-site

Full-time

Posted 28 days ago

Job description

AskBio Inc., a wholly owned and independently operated subsidiary of Bayer AG, is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular, central nervous system, cardiovascular, and metabolic disease indications with a clinical-stage pipeline that includes investigational therapeutics for congestive heart failure, limb-girdle muscular dystrophy, multiple system atrophy, Parkinson's disease, and Pompe disease. AskBio's gene therapy platform includes Pro10™, an industry-leading proprietary cell line manufacturing process, and an extensive array of capsids and promoters. With global headquarters in Research Triangle Park, North Carolina, and European headquarters in Edinburgh, Scotland, the company has generated hundreds of proprietary capsids and promoters, several of which have entered pre-clinical and clinical testing.
Our vision: Pioneering science to create transformative molecular medicines.
Our mission: Lead innovative science and drive clinical outcomes to transform people's lives.
Our principles:
  • Advance innovative science by pushing boundaries.
  • Bring transformative therapeutics to patients in need.
  • Provide an environment for employees to reach their fullest potential.

Our values:
  • Be a Pioneer. We are not afraid of the impossible and to innovate to make gene therapies accessible to those in need.
  • Cultivate Collaboration. Strive to be the best teammate, actively listen, openly communicate, and embrace diverse points of view.
  • Embrace Responsibility. We are humbled by the enormity of our mission. We hold a relentless commitment to advance science and clinical outcomes for our patients, families, and caregivers.
  • Raise the Bar. Continuously drive improvements and efficiencies. Seek and provide constructive feedback. Have a bias for learning and action.
  • Act with Uncompromising Integrity. Be honest, transparent, and committed to doing what's right in every situation. Make clear commitments and follow through.

Position Summary
AskBio is seeking a Manufacturing Science and Technology (MSAT) Process Engineer II to join our Process Engineering team and support current and future commercialization efforts. This position supports scale-up, technology transfer of AskBio's portfolio of gene therapy products into cGMP manufacturing for clinical production, process validation and commercial launch. The incumbent will onboard clinical programs into the MSAT laboratory, perform scale-up runs, and transfer programs to AskBio's contract manufacturing facility. Additionally, this position will be responsible for performing Phase III clinical enabling activities including scale-down model development and qualification, process characterization, and process control strategy definition to enable process performance qualification (PPQ) readiness for both drug substance and drug product manufacturing campaigns. This position is highly collaborative and will require internal and external team interactions to ensure successful process scale-up, technology transfers, and cGMP manufacturing operations to ensure continuity of supply while adhering to global regulations and standards.
This role is based on-site at our RTP (Research Triangle Park) Headquarters in NC and reports to an Associate Director, MSAT.
Job Responsibilities
  • Collaborate with cross-functional teams to transfer small-scale gene therapy processes from Process Development into the MSAT laboratory and subsequently perform scale-up and transfer to the cGMP manufacturing scale
  • Perform process characterization experiments to generate robustness data and define the process control strategy for PPQ manufacturing campaigns. Contribute to process characterization experimental design and data analysis
  • Develop and qualify small-scale models that are predictive of the cGMP manufacturing scale
  • Author technical protocols and reports to support experimental work and maintain clear, organized electronic laboratory notebooks
  • Provide effective communication of experimental results in technical presentations with internal stakeholders
  • Support investigations by contributing technical expertise to the root-cause analysis and using a data-driven approach for driving issue resolution
  • Ensure the laboratory is clean, organized and maintained in an efficient working order, includes scheduling routine preventative maintenance/calibration of instruments/equipment, securing supplies and materials for experiments, and proper scheduling of laboratory work

Minimum Requirements
  • [Bachelor's Degree in a scientific discipline and 2 years of Biopharmaceutical Experience OR Master's Degree in a scientific discipline and 0 years of Biopharmaceutical Experience
  • Hands-on upstream or downstream biomanufacturing laboratory experience
  • Excellent written and verbal communication skills, with experience interacting with a range of internal stakeholder groups
  • Proficiency in using Microsoft Office Suite (Word, Excel, PowerPoint)
  • Highly motivated, organized, and disciplined, with a strong desire to contribute as part of a best-in-class, collaborative tech transfer team
  • Adaptable and eager to learn, thriving in a fast-paced, highly interactive environment
  • Genuinely interested in building proficiency in upstream and downstream biomanufacturing operations, including process scale-up, technology transfer, process characterization, and process control strategy development
  • Continuous improvement-oriented, seeking opportunities to optimize process operations and performance through proactive problem solving
  • Open to domestic and international travel up to approximately 10%, as needed.

Preferred Education, Experience and Skills
  • Prior upstream experience
  • Some prior experience supporting cGMP manufacturing operations
  • Knowledge of the Design of experiment (DOE) methodology with an ability to design, execute, and analyze experiments with oversight. JMP Statistical Software proficiency is highly preferred

AskBio Inc. (AskBio) is an Equal Opportunity Employer and does not discriminate against any employee or applicant for employment because of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or any other protected status prohibited under Federal, State or local laws. All employment decisions are based on valid job-related requirements. If you are a qualified individual with a disability or a disabled veteran and are unable or limited in your ability to use or access our website, you may request a reasonable accommodation to express interest in a specific opening by calling us at (919) 561-6210 or sending us an email at careers@askbio.com.
Agencies: Please do not contact any employee at AskBio about this requisition. Any resume submitted by a recruitment agency to any employee at AskBio, through any medium, will be deemed the sole property of AskBio unless the agency was engaged by AskBio Talent Acquisition team to recruit for that position. All agencies must have a prior executed service agreement with AskBio prior to any search engagement. If a candidate who was submitted outside of the AskBio agency process is hired by AskBio, no fee or payment of any kind will be paid to the agency.

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