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Process Engineer Gene Therapy Jobs (NOW HIRING)

DivIHN

Process Engineer Pharmaceuticals I

NC · On-site

Client is seeking a contract Process Engineer/Research Associate to provide hands-on laboratory and manufacturing support of AAV (rAAV) vector research and late-stage clinical gene therapy programs.

Genezen

Process Engineer II

Lexington, MA · On-site

$85K - $110K/yr

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our ... The Process Engineer II plays a key role in supporting Genezen's gene therapy clinical/commercial ...

Genezen

Process Engineer II

Lexington, MA

$85K - $110K/yr

The field of gene therapy is growing rapidly and Genezen is here to meet the exacting needs of our ... The Process Engineer II plays a key role in supporting Genezen's gene therapy clinical/commercial ...

Clayco (LJC)

Process Engineer

Lenexa, KS · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Advanced therapy medicinal products (ATMPs), including cell and gene therapies * mRNA * Vaccines

Clayco (LJC)

Process Engineer

Chicago, IL · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Advanced therapy medicinal products (ATMPs), including cell and gene therapies * mRNA * Vaccines

Clayco (LJC)

Process Engineer

Lenexa, KS · On-site

The Process Engineer works closely with clients, process architects, utilities engineers ... Advanced therapy medicinal products (ATMPs), including cell and gene therapies * mRNA * Vaccines

Clayco (LJC)

Process Engineer

Greenville, SC

The Process Engineer works closely with clients, process architects, utilities engineers ... Advanced therapy medicinal products (ATMPs), including cell and gene therapies * mRNA * Vaccines

Clayco (LJC)

Process Engineer

Greenville, SC

The Process Engineer works closely with clients, process architects, utilities engineers ... Advanced therapy medicinal products (ATMPs), including cell and gene therapies * mRNA * Vaccines

Clayco (LJC)

Process Engineer

Lenexa, KS

The Process Engineer works closely with clients, process architects, utilities engineers ... Advanced therapy medicinal products (ATMPs), including cell and gene therapies * mRNA * Vaccines

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All JobsProcess Engineer Gene Therapy Jobs

Process Engineer Gene Therapy information

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$49.5K

$92K

$142.5K

How much do process engineer gene therapy jobs pay per year?

As of Jun 8, 2026, the average yearly pay for process engineer gene therapy in the United States is $92,018.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,500.00 and $103,000.00 per year, depending on experience, location, and employer.

How does a Process Engineer in Gene Therapy typically collaborate with cross-functional teams during process development?

As a Process Engineer in Gene Therapy, you will work closely with scientists, quality assurance specialists, manufacturing operators, and regulatory teams. Collaboration often involves coordinating process transfer, troubleshooting production issues, and aligning process improvements with regulatory requirements. You may participate in regular cross-functional meetings to ensure process changes maintain product integrity and compliance. This collaborative approach is essential to streamline development, scale-up, and commercialization of gene therapy products.

What is the difference between Process Engineer Gene Therapy vs Process Engineer Bioprocessing?

AspectProcess Engineer Gene TherapyProcess Engineer Bioprocessing
Required CredentialsBachelor's/Master's in Bioengineering, Chemical Engineering, or related; GMP trainingBachelor's/Master's in Bioengineering, Chemical Engineering, or related; GMP training
Work EnvironmentLaboratories, manufacturing facilities focused on gene therapy vectorsBiotech or pharmaceutical manufacturing plants, labs for biologics production
Industry UsagePrimarily in gene therapy and advanced therapeutics companiesBroader biopharmaceutical manufacturing, including vaccines and biologics

Process Engineer Gene Therapy and Process Engineer Bioprocessing share similar educational backgrounds and work environments. However, gene therapy engineers focus specifically on vector production and gene delivery systems, while bioprocessing engineers work on a wider range of biologics. Both roles require GMP knowledge and are vital in biotech manufacturing, but their specific applications differ based on product type.

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

To thrive as a Process Engineer in Gene Therapy, you generally need a degree in chemical engineering, biotechnology, or a related field, along with knowledge of bioprocessing and cGMP regulations. Experience with bioreactor systems, analytical tools like HPLC, and documentation software is typically required, and certifications such as Six Sigma or Lean Manufacturing are advantageous. Strong problem-solving skills, attention to detail, and effective teamwork and communication abilities help professionals excel in this role. These competencies ensure safe, efficient, and compliant development and manufacturing of gene therapy products, supporting both innovation and patient safety.

What does a Process Engineer in Gene Therapy do?

A Process Engineer in Gene Therapy is responsible for designing, developing, and optimizing manufacturing processes used to produce gene therapy products. They work to ensure that these processes are efficient, reproducible, and compliant with regulatory standards. Their duties often include scaling up laboratory methods to industrial production, troubleshooting process issues, and collaborating with scientists and quality teams to deliver safe and effective therapies to patients.
Infographic showing various Process Engineer Gene Therapy job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $92,018 per year, or $44.2 per hour.
Process Engineer - Drug Product

Process Engineer - Drug Product

Precigen, Inc

Germantown, MD • On-site

$90K - $110K/yr

Full-time

Posted 12 days ago

Job description

Job Description

Precigen is a dedicated commercial and clinical stage biopharmaceutical company advancing the next generation of gene therapies using precision technology to target the most urgent and intractable diseases in our core therapeutic areas of immuno-oncology, autoimmune disorders, and infectious diseases. Precigen has developed novel manufacturing processes to deliver UltraCAR-T® and AdenoVerse™ immunotherapies to patients.

The MS&T department is seeking a Process Engineer – Drug Product to support the Precigen, Inc. Drug Product Fill Finish activities that occur at a CMO. This position will require a professional who is technically savvy, thrives in a dynamic team environment, poses exceptional problem-solving skills, brings meticulous attention to detail in the quality of their work and is proactive in implementing improvements. This position will be supporting all technical aspects of Gene Therapy cGMP manufacturing of late clinical stage to commercialization of Adenovector products, including process transfer, process validation, continuous process verification, person in plant manufacturing support, and regulatory filings.


DUTIES AND RESPONSIBILITIES:

  • Responsible for end-to-end technical support of gene therapy product manufacturing (Drug Product Fill Finish), at CMOs.
  • Responsible for onsite Person in Plant activities at CMO locations DP Fill Finish.
  • Works cross functionally with Process Development, CMO, Quality Assurance, Quality Control, Supply Chain, and Validation departments to effectively transfer, implement and maintain processes at multiple facilities.
  • Works closely with the CMO to provide on-the-floor technical oversight through each product campaign startup as well as in response to any process/equipment troubleshooting requirements related to DP Fill Finish.
  • Collect and trend process data, perform process capability assessments, and identify areas for continuous improvement related to DP Fill Finish.
  • Authors and/or reviews technical reports, process tech transfer summary reports, risk assessments, master batch records, equipment user requirement specifications, and protocols in support of tech transfer, cGMP activities and regulatory filings.
  • Provide technical support for investigations and lend expertise in problem solving activities on existing production activities, determining root cause and corrective actions.
  • Lead / support process improvement projects, including new technologies for DP Fill Finish.
  • Offer subject matter expertise as a reviewer of project plans, technical reports/studies related to process understanding, regulatory submissions, and Validation protocols at CMO for DP Fill Finish.


EDUCATION AND EXPERIENCE:

  • B.Sc or M.Sc in Chemical Engineering, Bioengineering, Biotechnology or another relevant engineering / scientific qualification. Level will be determined based on education and experience.
  • 3-4 years of experience in a biopharmaceutical manufacturing setting where the individual has implemented process changes/optimization, technology transfer, and manufacturing support.
  • Experience in process development and/or process scale-up studies of Drug Product Fill Finish operations is a plus.
  • Experience summarizing and presenting data, statistical analysis, and authoring technical reports.
  • Strong computer skills with Microsoft Office, data trending/management software (Excel and Jmp) and the ability to quickly learn new applications.

DESIRED KEY COMPETENCIES:

  • Strong technical and scientific knowledge of drug product manufacturing operations.
  • Experience with manufacture of viral vectors and/or viral vaccines is a plus
  • Critical thinking and strong problem-solving skills with quantitative and analytical mind-set.
  • Self-organizer, meticulous hands-on habits, keen attention to detail.
  • Perform other responsibilities to support the needs of the department, as assigned.
  • Excellent interpersonal, verbal and written communication skills are essential in this collaborative work environment.
  • Experience with JMP statistical software
  • Knowledge and experience in Operational Excellence (OE) methodologies is a plus.
  • Maintains a high degree of ethical standard and trustworthiness.
  • Exhibits and open mindset when approaching challenges and conflict.
  • Demonstrates the ability to mentor and coach team members in all areas of expertise.
  • Working conditions and physical requirements:
    1. Must be able to lift, carry, push and/or pull 40 pounds of equipment or supplies.
    2. May need to work with hazardous materials.
    3. Able to stand up to 4 hours at a time.

EOE MFDV