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Biotech Process Engineer Jobs in Texas (NOW HIRING)

Facilities Engineer II

Houston, TX ยท On-site

$95 - $125/hr

... the validation process and/or requalifying assets ensure all validation deliverables and ... Bachelors degree in Biotechnology, Mechanical, Electrical, Chemical Engineering, or related field5 ...

Bachelors degree in Biotechnology, Mechanical, Electrical, Chemical Engineering, or related field ... Control process from initiation, revision of documents and processes up to training and ...

Validation Engineer II

Houston, TX ยท On-site

$85 - $120/hr

... process and ensure all validation deliverables and regulations have been met. The Validation ... Education in Biotechnology or a related major preferred5+ years experience in the pharmaceutical or ...

New

... process and ensure all validation deliverables and regulations have been met. The Validation ... Education in Biotechnology or a related major preferred * 5+ years experience in the pharmaceutical ...

Senior Mechanical/Piping Designer

Houston, TX ยท On-site +1

$55 - $75/hr

Prepare PFDs and P&IDs under supervision of process engineer. * Layout complex piping systems and ... Experience in the design of process support utilities in the pharmaceutical and biotech industries ...

The CQV Engineer develops the documentation to support Commissioning, Qualifications, and ... such as biotech, aseptic processing, aseptic fill/finish, OSD, Gene Therapy or equivalent ...

Quality Engineer I

Austin, TX ยท On-site

$71K - $92K/yr

Chemistry, Biology, Biotechnology, Engineering, or related scientific/technical discipline ... Familiarity with quality processes including incoming inspection, batch record review ...

Quality Engineer I

Austin, TX

$71K - $92K/yr

Chemistry, Biology, Biotechnology, Engineering, or related scientific/technical discipline ... Familiarity with quality processes including incoming inspection, batch record review ...

Identify, develop, and pursue new business opportunities across pharmaceutical, biotech ... Engineering, Process Engineering, Construction Management, or a related technical discipline.

... process improvements. * Deliver facilities support by coordinating infrastructure projects ... Bachelor's degree in Engineering, Biotechnology, or a related scientific/technical discipline.

Project Engineer- EPC

Dallas, TX ยท Hybrid

$150K/yr

... pharmaceutical, biotechnology, battery, data center, and mission-critical industries. This ... electrical, process, piping, instrumentation, controls, and other technical disciplines.

Embedded Software Enginner

Austin, TX ยท On-site

$130K - $171K/yr

... Diagnostics, Biotech, Research, Lab), Six Sigma/Lean, Finance/Accounting, Sales, and Marketing ... for embedded processors. - Prior experience working with SLIMbus will be ideal. - Clear ...

Embedded Software Enginner

Austin, TX ยท On-site

$130K - $171K/yr

... Diagnostics, Biotech, Research, Lab), Six Sigma/Lean, Finance/Accounting, Sales, and Marketing ... for embedded processors. - Prior experience working with SLIMbus will be ideal. - Clear ...

Showing results 41-60

Biotech Process Engineer information

See Texas salary details

$46.1K

$85.7K

$132.8K

How much do biotech process engineer jobs pay per year?

As of Aug 22, 2026, the average yearly pay for biotech process engineer in Texas is $85,729.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,400.00 and $96,000.00 per year, depending on experience, location, and employer.

What does a Biotech Process Engineer do?

A Biotech Process Engineer designs, develops, and optimizes processes used in the production of biological products such as pharmaceuticals, vaccines, and biofuels. They work closely with scientists and manufacturing teams to scale up lab procedures to industrial levels while ensuring product quality and regulatory compliance. Their role often involves troubleshooting equipment, improving efficiency, and implementing new technologies within biotech manufacturing environments.

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

To thrive as a Biotech Process Engineer, you need a solid background in chemical or biochemical engineering, process design, and regulatory compliance, typically supported by a relevant bachelor's or master's degree. Familiarity with process control systems, bioprocess simulation software, and industry-standard quality systems such as cGMP is essential. Strong analytical thinking, problem-solving abilities, and effective teamwork and communication skills help you excel in cross-functional environments. These skills ensure efficient, compliant, and innovative bioprocess operations, which are critical for product quality and organizational success.

What are some common challenges faced by Biotech Process Engineers during scale-up from laboratory to production?

Biotech Process Engineers often encounter challenges when scaling up processes from laboratory or pilot scale to full production. These challenges can include maintaining product consistency, ensuring process sterility, and adapting equipment to handle larger volumes without compromising yield or quality. Engineers must also collaborate closely with cross-functional teams such as quality assurance, validation, and manufacturing to implement changes efficiently and adhere to regulatory standards. Proactive problem-solving and strong communication skills are key to overcoming these hurdles and ensuring successful technology transfer.

What is the difference between Biotech Process Engineer vs Biotech Manufacturing Technician?

AspectBiotech Process EngineerBiotech Manufacturing Technician
CredentialsBachelor's degree in biotech, chemical engineering, or related field; often requires experience in process designAssociate's or bachelor's degree; focus on operational skills and equipment handling
Work EnvironmentDesigning, optimizing, and overseeing production processes in labs or manufacturing facilitiesOperating and maintaining equipment on the manufacturing floor
Job FocusProcess development, scale-up, troubleshooting, and process improvementExecuting production tasks, quality checks, and equipment setup

Biotech Process Engineers focus on designing and improving manufacturing processes, requiring technical and analytical skills. In contrast, Biotech Manufacturing Technicians handle day-to-day production operations. Both roles are essential in biotech manufacturing but differ in responsibilities and required qualifications.

What job categories do people searching Biotech Process Engineer jobs in Texas look for?

The top searched job categories for Biotech Process Engineer jobs in Texas are:

What cities in Texas are hiring for Biotech Process Engineer jobs?

Cities in Texas with the most Biotech Process Engineer job openings:

Infographic showing various Biotech Process Engineer job openings in Texas as of August 2026, with employment types broken down into 71% Full Time, and 29% Contract. Highlights an 94% In-person, and 6% Hybrid job distribution, with an average salary of $85,729 per year, or $41.2 per hour.

Facilities Engineer II

Immatics-US

Houston, TX โ€ข On-site

$95 - $125/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 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 OverviewWe are seeking a Facilities Engineer II to lead the implementation of new assets through the validation process and/or requalifying assets ensure all validation deliverables and regulations have been met, technically support cGMP Manufacturing and GxP operations with equipment issues, and manage Facility projects, as necessary.Schedule: Monday to Friday; 8:00 am โ€“ 5:00 pm; on-call support as neededReports to: Director, Facilities, Engineering, & Asset LifecycleLocation: 13203 Murphy Road Suite 100 Stafford, TX 77477Basic Qualifications:Bachelors degree in Biotechnology, Mechanical, Electrical, Chemical Engineering, or related field5+ years in pharmaceutical or biotech engineering within a GxP regulated manufacturing or laboratory environmentPreferred Qualifications:Demonstrated knowledge of FDA and cGMP requirementsApplied experience in good documentation practices and data integrity principles.An understanding of 21 CFR Part 11, 21 CFR Part 210, 21 CFR Part 211, EU Annex 1, and USPExperience in writing and reviewing Deviations and CAPAs, investigations resulting from OOS/OOT, environmental excursions, lab investigations leading to Change Controls for QMS.In this role you will:Draft validation documents including validation plans, user requirements specification (URS), risk assessments, configuration specification documents, installation qualification (IQ), operational qualification (OQ) and performance qualification (PQ) protocols, trace matrix and summary reports.Execute test scripts from IQ/OQ/PQ protocols using good documentation practices and provide appropriate supporting evidence.Create and manage project timelines and deliverables.Monitor and review Quality Management Systems (CAPA, Change Controls, Deviations) to ensure and maintain compliance with corporate and regulatory agency requirements.Contribute to the writing, coordination, review, and approval of Quality Events when needed.Coordinate, support, and investigate Corrective and Preventive Actions (CAPAs).Draft SOPs and work instructions for asset operation, maintenance, and cleaning.Assist in Change Control process from initiation, revision of documents and processes up to training and implementation.Assist in preparing QMS training materials and perform training as required.Support cross-functional groups for QMS functions and projects not limited to Asset Validation, Equipment Maintenance, Manufacturing, Quality Control, New Hire Onboarding, external and internal audits as needed.What do we offer?At Immatics, we believe in investing in our teamโ€™s health, safety and well-being. Hereโ€™s what you can expect if you join ImmaticsComprehensive Benefits:Competitive rates for Health, Dental, and Vision Insurance4 weeks of vacation, granted up front each year and prorated for first and last year of employment.12 company paid holidays7 days of sick time100% employer-paid life insurance up to at 1x annual salary, up to one hundred thousand dollars100% employer-paid short- and long-Term disability coverage401(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 OpportunityWe 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 AccommodationsWe 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 AuthorizationApplicants must be authorized to work in the United States without the need for current or future sponsorship.Pre-Employment RequirementsEmployment 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. #J-18808-Ljbffr