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

Initiate and manage RFI and RFP process and negotiate terms for all account programs and projects ... Biotech, Medical Device, and/or Clinical Research Organizations * Demonstrated track record of ...

Perform process scale-up, support technology transfer and provide manufacturing support at internal ... Biotechnology, Mathematics, Molecular Biology, Pharmaceutical Science, Statistics, or a related ...

Perform process scale-up, support technology transfer and provide manufacturing support at internal ... Biotechnology, Mathematics, Molecular Biology, Pharmaceutical Science, Statistics, or a related ...

... reagents and processes for high-efficiency production of antigens and antibodies. We are ... developed and produced. In addition, we offer pharmaceutical companies and biotechnology firms pre ...

... processes for high-efficiency production of antigens and antibodies. We are headquartered in ... developed and produced. In addition, we offer pharmaceutical companies and biotechnology firms pre ...

Showing results 41-60

Biotech Process Development information

See Houston, TX salary details

$18

$32

$47

How much do biotech process development jobs pay per hour?

As of Sep 7, 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 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 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 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 cities near Houston, TX are hiring for Biotech Process Development jobs?

Cities near Houston, TX with the most Biotech Process Development job openings:

Infographic showing various Biotech Process Development job openings in Houston, TX as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 15% Part Time, and 2% Contract. Highlights an 92% Physical, 3% Hybrid, and 5% Remote job distribution, with an average salary of $66,906 per year, or $32.2 per hour.

Global Head of CGT Operations Strategy & PMO

Lonza

Houston, TX • On-site

$250 - $350/hr

Other

Posted 20 days ago


Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical


Job description

Global Head of CGT Operations Strategy & PMO

United States, Houston (Texas)

Today, Lonza is a global leader in life sciences, operating across three continents. While our work is grounded in science, our success is driven by talented people collaborating to develop innovative solutions that help businesses bring therapies to patients. In return, we empower our employees to take ownership of their careers—encouraging ideas, both big and small, that make a meaningful impact on the world.

Our Specialized Modalities (SPM) platform is at the forefront of emerging technologies, spanning cell and gene therapy (CGT), microbial systems, and mRNA. We have supported over 450 process development projects, with a proven track record of translating cutting-edge science into scalable, advanced manufacturing solutions—enabled by modern, purpose-built facilities.

The Global Head of CGT Operations Strategy & PMO is responsible for leading operational excellence, transformation, and capability-building initiatives across the global Cell & Gene Therapy (CGT) network. This role ensures reliable operations, accelerates productivity improvements, advances digital transformation, and establishes training programs that enable sustainable performance, growth, and innovation.

By embedding best practices and harmonized operating approaches across all sites, this leader will drive operational reliability, flexibility, efficiency, and scalability while supporting the organization’s strategic growth objectives and long-term competitiveness.

Key Responsibilities
  • Define and execute the global CGT transformation strategy, including governance, prioritization, and long-term roadmap development.
  • Lead Operational Excellence, Digitalization, Training, and Productivity Improvement initiatives across the global manufacturing network.
  • Drive continuous improvement, productivity, cost optimization, and operational performance through Lean, Six Sigma, and other best-practice methodologies.
  • Champion digital transformation by implementing advanced technologies, automation, and data-driven solutions that improve reliability, efficiency, and flexibility.
  • Establish and oversee global training and capability-building programs to ensure workforce readiness and standardized competency development.
  • Identify, prioritize, and deliver high-impact strategic initiatives using robust project management and LBMS methodologies to achieve sustainable business outcomes.
  • Drive manufacturing innovation and adoption of emerging technologies and industry best practices to enhance scalability and competitiveness.
  • Lead, develop, and support global and site-based Operational Excellence, Transformation, Training, and Project Management teams.
  • Establish governance frameworks that promote harmonization, standardization, and consistent execution across all CGT sites.
  • Build strong partnerships with Manufacturing, MSAT, Quality, Regulatory, Engineering, EHS, Supply Chain, and Group Operations to ensure alignment and compliance.
  • Monitor, measure, and communicate the performance and business impact of transformation initiatives through KPIs, reporting, and governance reviews.
  • Serve as a key change leader, fostering a culture of operational excellence, accountability, collaboration, and continuous improvement throughout the global network.
Key Requirements & Skills
  • Bachelor’s degree in Science, Engineering, Technology, Business, Operations Management, or a related field required; advanced degree (MBA, Master’s, or equivalent) preferred.
  • Significant leadership experience within biopharmaceutical, biotechnology, cell and gene therapy, or other regulated manufacturing environments.
  • Proven success leading global Operational Excellence, productivity, and transformation programs across multi‑site manufacturing networks.
  • Deep expertise in Lean, Six Sigma, continuous improvement, process optimization, and operational performance management.
  • Strong knowledge of digital transformation, automation technologies, manufacturing systems, and data-driven decision-making.
  • Experience developing and implementing global training, capability-building, and workforce development programs.
  • Demonstrated ability to lead complex, cross‑functional initiatives that deliver measurable business value and sustainable results.
  • Strong understanding of GMP requirements, regulatory expectations, and quality systems within regulated manufacturing environments.
  • Strategic and global leader with strong business acumen, capable of translating enterprise strategy into actionable plans and driving organizational change.
  • Recognized people leader who builds high‑performing teams and fosters a culture of collaboration, agility, accountability, customer focus, integrity, and results.
Preferred Qualifications
  • Experience within Cell & Gene Therapy, biologics, advanced therapeutics, or highly regulated manufacturing environments.
  • Familiarity with Industry 4.0, digital manufacturing, advanced analytics, and automation technologies.
  • Experience leading large‑scale global transformation programs and organizational change initiatives.
  • Certification in Lean, Six Sigma, Project Management, or related disciplines preferred.

Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.

People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

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About Lonza

Sourced by ZipRecruiter

Industry

Biotechnology research and development and pharmaceutical and medicine manufacturing

Company size

10,000+ Employees

Headquarters location

Bern, KS, US