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Process Development Cell Gene Therapy Jobs in Chicago, IL

Gotion, Inc.

Process Engineer - Cell Line

Manteno, IL · On-site

... has R&D centers in Ohio, China, Japan and Europe. We innovate in the next generation electric ... Solve on-site process problems in the cell production line and regularly update the quality issue ...

Rush

Clinical Cell Therapy Lab Specialist

Chicago, IL · On-site

$29.36 - $47.79/hr

Cellular Processing and Manipulation • Perform a wide range of cellular therapy procedures in ... Cell enrichment or depletion techniques (e.g., CD34+ selection) o Multi-step or multi-day ...

Avalere Health

Creative Director

Chicago, IL · On-site

Specific experience in Gene Therapy/Sickle Cell, Rare Disease, and Multi-Cultural Marketing ... Directs the creative team through the concepting process, reviewing work and providing feedback ...

The University of Chicago

Research Technician

Chicago, IL · On-site

$18.50 - $25.50/hr

With a focus on CAR T-cell therapy for lymphoma and melanoma TIL therapy, our work has a ... Cell culture, including adherent and suspension cells, transfections, transductions, and gene ...

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Showing results 41-60

All JobsProcess Development Cell Gene Therapy JobsProcess Development Cell Gene Therapy Jobs in Chicago, IL

Process Development Cell Gene Therapy information

See Chicago, IL salary details

$19

$34

$51

How much do process development cell gene therapy jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for process development cell gene therapy in Chicago, IL is $34.70, according to ZipRecruiter salary data. Most workers in this role earn between $28.46 and $42.60 per hour, depending on experience, location, and employer.

What is the difference between Process Development Cell Gene Therapy vs Process Development Associate?

AspectProcess Development Cell Gene TherapyProcess Development Associate
CredentialsBachelor's/Master's in Biotechnology, Molecular Biology, or related fields; experience in cell therapy preferredBachelor's/Master's in Life Sciences; entry-level to mid-level experience in bioprocessing
Work EnvironmentLaboratories focused on cell therapy manufacturing, GMP facilitiesBiotech or pharmaceutical labs, manufacturing support roles
Industry UsagePrimarily in cell and gene therapy companies, biotech firmsBroadly in biotech, pharma, and contract manufacturing organizations

The Process Development Cell Gene Therapy role specializes in developing and optimizing processes for cell-based gene therapies, often requiring specific expertise in cell culture and GMP compliance. In contrast, the Process Development Associate has a broader scope, supporting various bioprocessing activities across different products. Both roles require strong laboratory skills, but the Cell Gene Therapy position emphasizes specialized knowledge in cell therapy manufacturing.

What are popular job titles related to Process Development Cell Gene Therapy jobs in Chicago, IL? For Process Development Cell Gene Therapy jobs in Chicago, IL, the most frequently searched job titles are:
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Senior Manager Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC)

AbbVie

North Chicago, IL • On-site

$124K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Re-posted 12 days ago

AbbVie rating

8.6

Company rating: 8.6 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

16th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
The Senior Manager Regulatory Affairs, Chemistry, Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients to deliver biologics products to patients, including mAb, ADC and cell & gene therapies. Prepares CMC regulatory strategies that enable first pass approvals. Develops and manages content strategy for regulatory submissions, including INDs/CTAs and amendments, new marketing applications and supplements/variations. Builds and maintains relationships within the Regulatory Affairs functional areas, Operations and Research & Development (R&D) organizations. Represents CMC on teams such as product development, Global Regulatory Product Teams and Operations brand teams to negotiate, influence, and provide strategic advice.
Responsibilities:
  • Prepares CMC regulatory product strategies. Prepares and manages regulatory submissions, including new applications and amendments, renewals annual reports, supplements and variations and responds to regulatory information
  • Analyzes and interprets information that impacts regulatory decisions. Seeks expert advice and technical support as required for strategies and submissions
  • Reviews and revises regulatory submissions to effectively present data and strategy to regulatory agencies
  • Responds to global regulatory information requests.
  • Develops strategies for CMC agency meetings, manages preparation for agency meetings, and manages content of pre-meeting submissions.
  • Manages products and change control with an understanding of regulations and company policies and procedures. Analyzes and approves manufacturing change requests.
  • Represents CMC regulatory affairs on teams such as the product development, Global Regulatory Product Teams and Operations brand teams, for assigned projects; negotiates with and influences team members with support of management to maximize chances for first pass approval of regulatory submissions
  • Stays abreast of regulatory procedures and changes in regulatory climate. Analyzes legislation, regulation and guidance, provides analysis to the organization
  • Develops, implements, and documents policies and procedures within the regulatory affairs department. Participates in initiatives internal to RA CMC.
    Represents CMC regulatory affairs on project initiatives with other functional areas to drive efficiencies across the company.
  • This role will work a hybrid work schedule (3 days in office & 2 days remote) from the Waltham, MA & Lake County, IL headquarters.

Significant Work Activities: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hr day) is required
Qualifications
  • Required Education: Bachelor's Degree in Pharmacy, Chemistry, Biology or Pharmacology, Engineering or related subject. Preferred Education: Relevant advanced degree preferred. Certification a plus.
  • Required Experience: 8 years pharmaceutical experience. Preferred Experience: 10 years pharmaceutical experience including 5-plus years in regulatory affairs or 5-plus years in Discovery, R&D, or Manufacturing.
  • Experience developing and implementing successful global regulatory strategies.
  • Experience working in a complex and matrix environment.
  • Strong oral and written communication skills.
  • Note: Higher education may compensate for years of experience

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our long-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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