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Biotech Process Development Jobs in Texas (NOW HIRING)

Radiomedix, Inc.

Radiochemist

Houston, TX · On-site

Radiochemist RadioMedix Inc., a Biotechnology Company headquartered in Houston, Texas, is seeking ... The successful candidate will play a key role in process development, radioisotope and ...

Radiomedix, Inc.

Radiochemist

Houston, TX · On-site

Radiochemist RadioMedix Inc., a Biotechnology Company headquartered in Houston, Texas, is seeking ... The successful candidate will play a key role in process development, radioisotope and ...

Apply Early

IQVIA

CRA 2, IQVIA Biotech

Dallas, TX

$71K - $145K/yr

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

IQVIA

CRA 2, IQVIA Biotech

Dallas, TX · On-site

$71K - $145K/yr

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

IQVIA

CRA 1, IQVIA Biotech

Houston, TX · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

CRA 1, IQVIA Biotech

Austin, TX · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

CRA 2, IQVIA Biotech

Houston, TX

$71K - $145K/yr

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

IQVIA, Inc.

CRA 2, IQVIA Biotech

Houston, TX · On-site

$71K - $145K/yr

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

IQVIA

CRA 2, IQVIA Biotech

Houston, TX

$71K - $145K/yr

We create intelligent connections to accelerate the development and commercialization of innovative ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

IQVIA

CRA 1, IQVIA Biotech

Dallas, TX · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

CRA 1, IQVIA Biotech

San Antonio, TX · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

CRA 1, IQVIA Biotech

Fort Worth, TX · On-site

$71K - $145K/yr

... level financial processes or startup activities based on study needs. Accurate and timely ... We create intelligent connections to accelerate the development and commercialization of innovative ...

IQVIA

Sr. CRA 1, Oncology, IQVIA Biotech

San Antonio, TX

$87K - $169K/yr

Responsibilities Essential Functions If applicable, may be accountable for supporting development ... IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for ...

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All JobsBiotech Process Development JobsBiotech Process Development Jobs in Texas

Biotech Process Development information

See Texas salary details

$17

$28

$39

How much do biotech process development jobs pay per hour?

As of Jul 6, 2026, the average hourly pay for biotech process development in Texas is $28.57, according to ZipRecruiter salary data. Most workers in this role earn between $24.90 and $31.54 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 Texas? For Biotech Process Development jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Biotech Process Development jobs in Texas look for? The top searched job categories for Biotech Process Development jobs in Texas are:
What cities in Texas are hiring for Biotech Process Development jobs? Cities in Texas with the most Biotech Process Development job openings:
Biotech Process Development jobs near you
Infographic showing various Biotech Process Development job openings in Texas as of June 2026, with employment types broken down into 82% Full Time, 15% Part Time, 2% Contract, and 1% Nights. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $59,431 per year, or $28.6 per hour.
Radiochemist

Radiochemist

Radiomedix, Inc.

Houston, TX • On-site

Full-time

Posted 29 days ago

Job description

Radiochemist
RadioMedix Inc., a Biotechnology Company headquartered in Houston, Texas, is seeking an experienced Radiochemist to work in our Research and Development Team at our corporate office. The successful candidate will play a key role in process development, radioisotope and radiopharmaceutical manufacturing, and life-cycle management of GMP products. This position will focus on high-priority projects at RadioMedix that will be integral to upcoming clinical drug trials. This is a newly created position with potential for significant growth.
We're a growing company and we continue to add talent from a variety of fields. RadioMedix seeks to hire highly motivated and forward-thinking professionals interested in nuclear medicine research and development and influencing change within the nuclear medicine landscape.
Roles/Deliverables
The Radiochemist will provide technical expertise to support the development of methodologies and procedures for chemical and radiochemical handling, of remote handling systems, and of radiochemical separations. They will also support the development and validation of analytical and radioanalytical methods and procedures that will be used to demonstrate Manufacturing and Quality Control (QC) over radioisotope and radiopharmaceutical production processes. The Radiochemist will support the implementation of Laboratory Information Management Systems (LIMS) and quality assurance procedures under 21 CFR 211, and ICH guidelines.
Research
  • Develop radiopharmaceuticals to support RadioMedix's new product pipeline
  • Propose, develop, and conduct experiments to support design, scale-up, start-up, and ongoing production of radioisotopes
  • Develop and optimize radiolabeling procedures and analytical/radioanalytical methods
  • Utilize a broad spectrum of analytical techniques/instrumentation (i.e., ICP-MS, ICP-OES, HPLC, iTLC, alpha/beta spectroscopy, gamma spectroscopy, and wet chemistry techniques)
  • Develop associated analytical methods for characterization of radiolabeled products
  • Perform development and validation of RMX radiopharmaceuticals
  • Troubleshoot radiochemical reactions, radiochemical separations, and automated systems
  • Execute engineering runs and process validations
  • Technical writer and reviewer of validation documentation, Standard Operating Procedures (SOPs), and other quality documents
  • Train team members in laboratory procedures and equipment
  • Supervise the work of team members and assign tasks as needed
  • Provide leadership and mentoring to team members
  • Supper new product development, assist in management multiple projects, and contribute to team based investigations
  • Ensure compliance with environment, safety, health, and quality program requirements
Production/Manufacturing
  • Proficient in utilizing manipulators during production
  • Proficient in synthesizer machines (i.e., Trasis All-in-one, mini-All-in-one) for new product development
  • Provide training to team members in the use of synthesizer machines
  • Manufacture radiopharmaceuticals including Ga68PSMA
  • Calibrate manufacturing and quality control instrumentation
  • Perform OOS investigations and CAPAs
Opportunity for growth
  • Opportunity to grow the R&D team with room for advancement in the company
  • Cross-functional work to support current and new products as needed
  • Potential to a drug product manufacturing team
Minimum Requirements
  • Ph.D. in Chemistry, Biology, Microbiology, and or life sciences.
  • Radiochemistry experienced preferred
  • Minimum 10 year's experience in pharma/laboratory management and/or related pharma experience
  • Thorough knowledge of cGMPs, GLPs, and pharma manufacturing
  • Ability to collaborate with cross-functional teams including research, process development, quality assurance and quality control.
  • Demonstrated proficiency in root cause analysis as applied in a pharma environment
  • Excellent problem solving, communication, and decision-making skills
  • Computer skills, and knowledge of document management/quality systems
  • Experience working and communicating productively in a multidisciplinary team.
  • Perform all work in compliance with site safety and radiation protection guidelines.
  • Strong organizational and communication skills including technical writing, presentation, and interpersonal skills

Disclaimer
This position is not eligible for employer-sponsored work authorization. Candidates must be authorized to work in the United States on a permanent basis without the need for current or future sponsorship.

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