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Biotech Process Development Jobs in Houston, TX (NOW HIRING)

Immatics NV

Senior CMC Program Manager

Houston, TX · On-site

$110K - $111K/yr

... within biotechnology, pharmaceutical, or oncology-focused clinical development environments ... Drive collaboration across Manufacturing, Process Development, Analytical Development, Quality ...

Immatics NV

Senior CMC Program Manager

Houston, TX

$110K - $111K/yr

... within biotechnology, pharmaceutical, or oncology-focused clinical development environments ... Drive collaboration across Manufacturing, Process Development, Analytical Development, Quality ...

Baylor Genetics

Automation Engineer III

Houston, TX · On-site

COMPETENCIES * Extensive experience in a biotechnology environment, showcasing mastery in ... Proven track record in method development on automation platforms and driving process improvements.

ACROBIOSYSTEMS INC

Associate Regional Manager

Houston, TX · Remote

$80K - $95K/yr

Our mission is to accelerate the process of target therapeutic drug development. We aim to be a ... This includes a broad range of customers across academia, government, biotech, and pharma. You will ...

Baylor Genetics

Automation Engineer II

Houston, TX · On-site

Analyze operational data and identify opportunities for process improvement and increased system ... Experience working in a biotechnology, clinical laboratory, or related environment. * Experience ...

ACROBIOSYSTEMS INC

Associate Regional Manager

Houston, TX · Remote

$80K - $95K/yr

Our mission is to accelerate the process of target therapeutic drug development. We aim to be a ... This includes a broad range of customers across academia, government, biotech, and pharma. You will ...

JoVE

Director of Sales, Biopharma

Houston, TX · On-site

... and biotech organizations. * Monitor pipeline health, forecast accuracy, and deal progression ... Strong experience managing long sales cycles and multi-stakeholder buying processes. * Data-driven ...

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All JobsBiotech Process Development JobsBiotech Process Development Jobs in Houston, TX

Biotech Process Development information

See Houston, TX salary details

$18

$32

$47

How much do biotech process development jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for biotech process development in Houston, TX is $32.17, according to ZipRecruiter salary data. Most workers in this role earn between $26.39 and $39.47 per hour, depending on experience, location, and employer.

What is biotech process development?

Biotech process development refers to the design, optimization, and scale-up of manufacturing processes used to produce biological products, such as pharmaceuticals, enzymes, or vaccines. Professionals in this field work to turn laboratory procedures into efficient, large-scale industrial processes that meet regulatory and quality standards. This often involves selecting suitable equipment, optimizing conditions, ensuring reproducibility, and troubleshooting production issues. The ultimate goal is to produce high-quality products safely, consistently, and cost-effectively.

What is the difference between Biotech Process Development vs Biotech Manufacturing Associate?

AspectBiotech Process DevelopmentBiotech Manufacturing Associate
Primary FocusDesigning, optimizing, and scaling up bioprocesses for product developmentExecuting manufacturing processes to produce biopharmaceuticals at scale
Work EnvironmentLaboratories and pilot plant facilitiesProduction floors and manufacturing plants
Required SkillsProcess design, lab techniques, troubleshootingEquipment operation, quality control, adherence to SOPs
Typical CredentialsBSc/MSc in Biotechnology, Chemical Engineering, or related fieldsBSc in Biotechnology, Biology, or related fields

While both roles are essential in biotech, Biotech Process Development focuses on creating and optimizing processes during product development, whereas Biotech Manufacturing Associates handle the day-to-day production to ensure consistent product quality at scale.

What are the key skills and qualifications needed to thrive in Biotech Process Development, and why are they important?

To excel in Biotech Process Development, you need a strong background in bioprocess engineering, molecular biology, and chemistry, typically supported by a degree in biotechnology or related fields. Familiarity with tools such as bioreactors, chromatography systems, and data analysis software, along with certifications in Good Manufacturing Practice (GMP), is highly valuable. Strong problem-solving skills, attention to detail, and effective teamwork distinguish top performers in this role. These competencies are crucial for optimizing processes, ensuring product quality, and driving innovation in the biotech industry.

What are some common challenges faced by professionals in Biotech Process Development, and how are they typically addressed?

Professionals in Biotech Process Development often encounter challenges related to scaling up processes from the laboratory to commercial production, ensuring product consistency, and meeting strict regulatory standards. Addressing these challenges typically involves close collaboration with cross-functional teams such as quality assurance, regulatory affairs, and manufacturing. Continuous process optimization, thorough documentation, and robust validation protocols are essential strategies to overcome these hurdles and ensure successful product development and commercialization.
What are popular job titles related to Biotech Process Development jobs in Houston, TX? For Biotech Process Development jobs in Houston, TX, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Houston, TX look for? The top searched job categories for Biotech Process Development jobs in Houston, TX are:
What cities near Houston, TX are hiring for Biotech Process Development jobs? Cities near Houston, TX with the most Biotech Process Development job openings:
Biotech Process Development jobs near you
Infographic showing various Biotech Process Development job openings in Houston, TX as of June 2026, with employment types broken down into 83% Full Time, 15% Part Time, and 2% Contract. Highlights an 85% Physical, 2% Hybrid, and 13% Remote job distribution, with an average salary of $66,906 per year, or $32.2 per hour.

Senior CMC Program Manager

Immatics NV

Houston, TX • On-site

$110K - $111K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 9 days ago

Job description

Join Immatics and shape the future of cancer immunotherapy; one patient at a time!
Immatics is committed to making a meaningful impact on the lives of patients with cancer. We are the global leader in precision targeting of PRAME, a target expressed in more than 50 cancers. Our cutting-edge science and robust clinical pipeline form the broadest PRAME franchise with the most PRAME indications and modalities, spanning TCR T-cell therapies and TCR bispecifics.
Why Join Us?
  • Innovative Environment: Help to pioneer advancements in cancer immunotherapy.
  • Collaborative Culture: Be part of a diverse team dedicated to your professional growth.
  • Global Impact: Contribute to therapies that make a lasting impact on patients globally.

Role Overview:
We are seeking a Senior Program Manager, CMC to lead and coordinate cross-functional Chemistry, Manufacturing, and Controls (CMC) activities within a cell therapy development and manufacturing environment. The Senior Program Manager, CMC will drive planning, execution, and integration across manufacturing, analytical, quality, regulatory, and supply chain functions to support clinical development and commercialization goals. This role serves as a strategic partner across technical and operational teams, ensuring alignment, proactive risk management, and readiness for key milestones, including regulatory submissions and commercial manufacturing.
Reports to: Senior Director
Location: 13203 Murphy Road Suite 100 Stafford, TX 77477
Basic Qualifications:
  • Master's degree in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or a related field
  • 6+ years of experience in CMC program/project management or complex project leadership within biotechnology, pharmaceutical, or oncology-focused clinical development environments
  • Demonstrated experience leading cross-functional CMC activities, including manufacturing, quality, analytical, and regulatory operations
  • Academic or industry experience in cell and gene therapy, immunology/oncology, or bioprocessing/manufacturing sciences
  • Proven leadership, stakeholder management, and organizational skills with the ability to manage competing priorities in fast-paced environments

Preferred Qualifications:
  • PhD in life sciences, medicine, immunology, oncology, pharmacy, health sciences, or a related field
  • Experience supporting late-stage CMC programs in immunology, oncology, or cell and gene therapy
  • Proven experience managing complex programs and critical paths across multiple technical and operational functions
  • Proficiency with project management tools, dashboards, and reporting systems in regulated environments
  • Advanced ability to identify risks, drive decision-making, and implement process improvements across cross-functional teams
  • Experience coordinating external vendors, CMOs, CDMOs, or consulting partners
  • Strong communication and presentation skills with experience supporting senior leadership discussions and strategic planning

In this role you will:
  • Develop and maintain CMC program plans, timelines, risk registers, trackers, and reporting tools to support integrated program execution
  • Manage CMC deliverables, milestones, and critical paths while ensuring alignment with overarching development program timelines
  • Lead and facilitate cross-functional CMC meetings, including agenda development, documentation, action tracking, and follow-up activities
  • Drive collaboration across Manufacturing, Process Development, Analytical Development, Quality, Regulatory, Supply Chain, and Patient Operations teams
  • Coordinate and oversee activities with external vendors, contractors, CMOs, and CDMOs
  • Support strategic planning, governance, and decision-making activities with department leaders and senior management
  • Contribute to continuous improvement of CMC program management tools, processes, onboarding, and operational best practices

What do we offer?
At Immatics, we believe in investing in our team's health, safety and well-being. Here's what you can expect if you join Immatics
Comprehensive Benefits:
  • Competitive rates for Health, Dental, and Vision Insurance
  • 4 weeks of vacation, granted up front each year and prorated for first and last year of employment.
  • 12 company paid holidays
  • 7 days of sick time
  • 100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars
  • 100% employer-paid short- and long-Term disability coverage
  • 401(k) with immediate eligibility and company match...
    • The company will match 100% of your contributions up to 3% of your base salary for the first two years of employment, 4% for years 2-3 of employment, and up to 5% of your salary from the fourth year onward of continued employment.
  • Partially paid parental leave for eligible employees.
  • Additional voluntary employee-paid benefits and services, including accident, hospital indemnity, and critical illness insurance, as well as identity theft protection and pet insurance.

Equal Employment Opportunity
We are an equal opportunity employer and are committed to building a diverse and inclusive workplace. We consider all qualified applicants for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, national origin, ancestry, age, marital status, disability, genetic information, veteran status, or any other status protected by applicable law.
Reasonable Accommodations
We are committed to providing reasonable accommodations to individuals with disabilities and to applicants with sincerely held religious beliefs, practices, or observances. If you require assistance or accommodation during the application or interview process, please contact us at RecruitingUS@immatics.com.
Work Authorization
Applicants must be authorized to work in the United States without the need for current or future sponsorship. Visa sponsorships may be available for certain roles.
Pre-Employment Requirements
Employment is contingent upon successful completion of a background check, reference checks and pre-employment drug screening, where permitted by applicable law. For certain roles, additional screenings such as a credit check or motor vehicle record review may be required, where job-related and consistent with business necessity.

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