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Phd Chemical Engineer Jobs in Raleigh, NC (NOW HIRING)

Engineering Grad Co-op

Holly Springs, NC · On-site

$35.34 - $41.20/hr

D. for a PhD internship from an accredited college or university and completion of the first year ... Degree concentration(s) in Engineering (Chemical, Mechanical, Biomedical, Electrical), Construction ...

Engineering Grad Co-op

Holly Springs, NC · On-site

$35.34 - $41.20/hr

D. for a PhD internship from an accredited college or university and completion of the first year ... Degree concentration(s) in Engineering (Chemical, Mechanical, Biomedical, Electrical), Construction ...

PhD with relevant experience or MS with 3+ years of experience in Biology, Biochemistry, Molecular Biology, Chemical Engineering, Immunology, or a related life science field, preferably within ...

Bachelor's biochemistry, chemical engineering, bioengineering, or related technical field with 4-6 years relevant experience or Master's with 2-4 or PhD with 0-2. * Extensive experience with ...

Senior Industrial Hygienist

Raleigh, NC · On-site

$15.75 - $19.75/hr

Perform field studies including airborne chemical monitoring, noise monitoring, indoor air quality ... Our professionals include environmental architects, archaeologists, biologists, engineers ...

Senior Industrial Hygienist

Raleigh, NC · On-site

$15.75 - $19.75/hr

Perform field studies including airborne chemical monitoring, noise monitoring, indoor air quality ... Master's degree or PhD preferred. * A valid driver's license with acceptable violation history may ...

Showing results 21-39

Phd Chemical Engineer information

See Raleigh, NC salary details

$38.9K

$85K

$136.1K

How much do phd chemical engineer jobs pay per year?

As of Sep 4, 2026, the average yearly pay for phd chemical engineer in Raleigh, NC is $85,044.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,600.00 and $103,500.00 per year, depending on experience, location, and employer.

What does a PhD chemical engineer do?

A PhD Chemical Engineer conducts advanced research and develops processes involving the transformation of raw materials into useful products, often working in industries such as pharmaceuticals, energy, or materials science. They design experiments, analyze data, and solve complex problems related to chemical processes, often collaborating with multidisciplinary teams. Their work can also include teaching, publishing research, and leading innovative projects in academia or industry.

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

To thrive as a PhD Chemical Engineer, you need advanced knowledge of chemical engineering principles, research methodology, and a doctoral degree in chemical engineering or a related field. Proficiency in simulation software (like Aspen Plus, MATLAB, or COMSOL), laboratory instrumentation, and data analysis tools is typically required. Strong problem-solving, critical thinking, and effective communication skills help you collaborate with multidisciplinary teams and disseminate research findings. These competencies are crucial for driving innovation, successfully managing complex projects, and contributing to advancements in the chemical engineering field.

What are the typical interdisciplinary collaborations a PhD chemical engineer can expect in industry or academia?

PhD Chemical Engineers frequently collaborate with professionals from diverse fields, such as mechanical engineers, materials scientists, biologists, and data scientists. These collaborations are essential, as many projects—like process optimization, product development, or sustainability initiatives—require expertise beyond chemical engineering. Effective teamwork is often fostered through cross-functional project meetings, joint research efforts, and shared laboratory spaces. Engaging in interdisciplinary work not only broadens your technical knowledge but also enhances your problem-solving skills and opens up new career advancement opportunities.

What is the difference between Phd Chemical Engineer vs Chemical Engineer?

AspectPhd Chemical EngineerChemical Engineer
Required CredentialsPhD in Chemical Engineering or related fieldBachelor's or Master's in Chemical Engineering
Work EnvironmentResearch labs, academia, R&D departmentsManufacturing plants, process design, industrial settings
Employer & Industry UsageUniversities, research institutions, advanced R&DChemical, petrochemical, pharmaceuticals, manufacturing

The main difference between a Phd Chemical Engineer and a Chemical Engineer lies in their education level and work focus. Phd Chemical Engineers typically engage in research, development, and academia, requiring a doctoral degree. Chemical Engineers usually hold a bachelor's or master's degree and work in process design, manufacturing, and industrial applications. Both roles are vital in the chemical industry but serve different purposes based on expertise and work environment.

What cities near Raleigh, NC are hiring for Phd Chemical Engineer jobs?

Cities near Raleigh, NC with the most Phd Chemical Engineer job openings:

Infographic showing various Phd Chemical Engineer job openings in Raleigh, NC as of August 2026, with employment types broken down into 79% Full Time, 10% Part Time, and 11% Contract. Highlights an 90% In-person, 4% Hybrid, and 6% Remote job distribution, with an average salary of $85,044 per year, or $40.9 per hour.

Associate Director or Director, CMC Regulatory Affairs (Durham)

Atsena

Durham, NC • On-site

Full-time

Re-posted 12 days ago


Job description

Position Summary

The Associate Director / Director, CMC Regulatory Affairs will lead global CMC regulatory strategy and execution for the company’s gene therapy programs from early research through clinical development and commercialization. This role is responsible for developing CMC regulatory strategies across product development stages, supporting regulatory submissions, and serving as the regulatory liaison to internal CMC teams and external contract manufacturing organizations.

The individual will work cross-functionally with process development, analytical development, manufacturing, quality, and program leadership to ensure that CMC development plans meet regulatory expectations for gene therapy products. The role will also support interactions with global regulatory authorities such as the U.S. Food and Drug Administration and the European Medicines Agency.

Key Responsibilities CMC Regulatory Strategy
  • Develop and implement global CMC regulatory strategies for gene therapy programs from early development through clinical stages and commercialization.
  • Provide regulatory guidance on viral vector manufacturing, process development, analytical characterization, and product comparability.
  • Assess regulatory risks related to manufacturing changes and propose mitigation strategies.
Regulatory Submissions
  • Lead preparation and review of CMC sections of global regulatory submissions, including: INDs and IND amendments, CTAs and IMPDs, BLA/MAA submissions and supplements, annual reports and regulatory updates
  • Ensure submissions meet regulatory expectations for gene therapy products.
Health Authority Interactions
  • Prepare CMC regulatory briefing documents and support agency meetings.
  • Serve as the subject matter expert for CMC topics during interactions with agencies including the FDA and EMA.
  • Coordinate and author responses to regulatory agency questions related to CMC.
Cross-Functional Collaboration
  • Partner closely with internal teams including: Process Development, Analytical Development, Manufacturing, Quality
  • Serve as the CMC regulatory representative on cross-functional program teams.
  • Provide regulatory guidance for manufacturing changes, comparability strategies, and lifecycle management.
Regulatory Intelligence & Compliance
  • Monitor evolving regulatory guidance related to gene therapy and advanced biologics.
  • Interpret regulatory requirements and communicate implications to internal teams.
  • Support development of internal regulatory policies and processes.
Qualifications Education
  • PhD or MS in biochemistry, molecular biology, chemical engineering, pharmaceutical sciences, or related field.
Preferred Qualifications
  • Direct experience with AAV, lentiviral, or other gene therapy platforms.
  • Experience supporting late-stage development or BLA/MAA submissions.
  • Familiarity with global regulatory frameworks for advanced therapy medicinal products (ATMPs).
  • Prior experience participating in regulatory meetings.
Associate Director Experience
  • 7–10 years of experience in regulatory affairs and CMC.
  • Experience contributing to CMC sections of IND/CTA submissions.
Director Experience
  • 10–15+ years of experience in regulatory affairs with leadership responsibility for CMC regulatory strategy.
  • Demonstrated experience leading CMC regulatory submissions and health authority interactions.
Knowledge & Skills
  • Strong knowledge of global CMC regulatory requirements for biologics and gene therapies.
  • Understanding of viral vector manufacturing processes.
  • Experience with analytical characterization, comparability, and manufacturing changes.
  • Excellent regulatory writing and communication skills.
  • Ability to work effectively in a fast-paced startup environment.
Key Competencies
  • Strategic thinking and problem solving
  • Strong scientific and regulatory expertise
  • Cross-functional leadership
  • Excellent communication and collaboration skills
  • Ability to manage multiple programs and timelines
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