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Director Bioanalytical Jobs in Texas (NOW HIRING)

... and bioanalytical measurements. We are a leading global manufacturer and service provider of ... direct authority. * Orchestrates manufacturing, quality, regulatory, supply chain, and product ...

... and bioanalytical measurements. We are a leading global manufacturer and service provider of ... direct authority. * Orchestrates manufacturing, quality, regulatory, supply chain, and product ...

Director Bioanalytical information

See Texas salary details

$25.9K

$121.9K

$195.2K

How much do director bioanalytical jobs pay per year?

As of Sep 8, 2026, the average yearly pay for director bioanalytical in Texas is $121,933.00, according to ZipRecruiter salary data. Most workers in this role earn between $78,269.00 and $157,418.00 per year, depending on experience, location, and employer.

What is a director bioanalytical?

A Director Bioanalytical oversees bioanalytical strategy, laboratory operations, and regulatory compliance for drug development and research. They manage assay development, validation, and sample analysis to support preclinical and clinical studies. This role requires expertise in bioanalytical techniques such as LC-MS/MS, ELISA, and biomarker analysis. Additionally, they ensure compliance with GLP/GCP guidelines and collaborate with cross-functional teams to drive scientific decision-making.

What are the typical daily responsibilities of a director bioanalytical?

As a Director Bioanalytical, your daily responsibilities often include overseeing the planning and execution of bioanalytical studies, ensuring compliance with regulatory standards, and managing a team of scientists and support staff. You’ll review and interpret complex data, troubleshoot analytical challenges, and coordinate closely with project managers, regulatory affairs, and external partners. Additionally, you’ll be involved in developing and validating new analytical methods and contributing to strategic decisions that support drug development pipelines. This dynamic role combines hands-on scientific oversight with high-level team leadership and cross-functional collaboration.

What are the key skills and qualifications needed to thrive in the director bioanalytical position, and why are they important?

To thrive as a Director Bioanalytical, you need advanced expertise in bioanalytical chemistry, method development, and regulatory compliance, typically supported by a graduate degree in a related scientific field. Familiarity with analytical platforms such as LC-MS/MS, laboratory information management systems (LIMS), and relevant regulatory guidelines (FDA, EMA) is essential. Strong leadership, project management, and effective communication skills distinguish top candidates in this role. These abilities are vital to overseeing complex studies, ensuring data integrity, and leading multidisciplinary teams in a high-stakes environment.

What job categories do people searching Director Bioanalytical jobs in Texas look for?

The top searched job categories for Director Bioanalytical jobs in Texas are:

Infographic showing various Director Bioanalytical job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 12% Part Time, 3% Contract, and 1% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $121,933 per year, or $58.6 per hour.

Research Postdoctoral Fellow II

Texas Southern University

Houston, TX • On-site

$60 - $80/hr

Other

Posted 6 days ago


Job description

Job Title

Research Postdoctoral Fellow II – Official TSU Title

Job Description Summary

Under direct supervision of the U54 grant PI, this position conducts pharmaceutical science research in the Center for Biomedical and Health Research (CBMHR). Responsibilities include bioanalysis, drug absorption studies using Caco‑2 and intestinal perfusion models, drug metabolism using enzyme‑mediated models, metabolite structure identification, drug elimination and biodistribution using animal models, and providing services and technical support to internal and external users. This grant‑funded position supports the research and development activities of the university’s large center grants, including the NIH U54 RCMI‑CBMHR Center, CPRIT CCPF Center, the iO3 Center, and TSU’s Catalyst. The postdoctoral fellow assists in grant and paper writing, presents research at local, national and international meetings, and provides help in lab maintenance.

Responsibilities
  • Operate, maintain, and conduct bioanalysis using Waters Acquity UPLC, Sciex tripleQ, and high‑resolution LC‑MS/MS equipment in the RCMI‑CBMHR core facility.
  • Conduct drug absorption studies using the Caco‑2 cell culture, transporter vesicle membrane, and intestinal perfusion models.
  • Lead advanced drug metabolism research, including preparation and characterization of tissue microsomes, development of in‑vitro metabolism assays, and evaluation of metabolic pathways and enzyme kinetics; conduct metabolite structure identification using LC‑MS, NMR, etc.
  • Complete cell culture for in‑vitro ADME studies ensuring compliance with best practices, quality standards, and safety regulations.
  • Maintain all CBMHR instruments, develop and implement comprehensive record‑keeping and compliance frameworks for program participants, staff, equipment inventories, and compliance activities.
  • Prepare and review facility activity reports, research activity summaries, operational status documents, instrument usage statistics, and program status reports for users, university, and funding agencies.
  • Assist PIs in preparation of progress reports and grant deliverables, ensuring scientific accuracy and timely submission.
  • Publish data and publications in peer‑reviewed journals, present at conferences, and actively pursue external funding opportunities.
  • Provide advanced training, mentorship, and supervision to undergraduate and graduate students, technical staff, and junior scientists.
  • Perform other job‑related duties as assigned.
Employment Details

FTE: 1.0

Salary Range: $64,197.37 – $81,851.64

Hours of Work: 8:00 AM – 5:00 PM, Monday‑Friday

Education

Required: Doctoral degree in a biomedical science‑related field with experience in pharmaceutical research.

Required Licensing/Certification

None required.

Knowledge, Skills, and Abilities

Knowledge of:

  • Biostatistical analysis supporting biomedical/​pharmaceutical research.
  • Technical and functional principles and procedures.
  • Microsoft Office Professional or similar applications.

Skill in:

  • Details oriented.
  • Problem‑solving and decision‑making.
  • Multitasking and time management.
  • Verbal and written communication.

Ability to:

  • Operate software.
  • Maintain the security or integrity of critical infrastructure, including communications systems, computer networks, cybersecurity systems, electric grids, hazardous waste treatment, or water treatment systems.
Preferred Experience
  • At least 3 peer‑reviewed publications as primary author.
  • Experience with analytical instrumentation, ADME and PK research, animal handling, medicinal chemistry, etc.
Working/Environmental Conditions

Work performed in a routine office environment with no exposure to hazardous or unpleasant conditions. Physical demands are typically limited to sitting or standing for extended periods; occasional stooping, lifting or carrying light objects may be required.

UA EEO Statement

It is the policy of Texas Southern University to provide a work environment that is free from discrimination for all persons regardless of race, color, religion, sex, age, national origin, individuals with disability, sexual orientation, or protected veteran status in its programs, activities, admissions or employment policies. This policy of equal opportunity is strictly observed in all University employment‑related activities such as advertising, recruiting, interviewing, testing, employment training, compensation, promotion, termination, and employment benefits. This policy expressly prohibits harassment and discrimination in employment based on race, color, religion, gender, gender identity, genetic history, national origin, individuals with disability, age, citizenship status, or protected veteran status. This policy shall be adhered to in accordance with the provisions of all applicable federal, state and local laws, including, but not limited to, Title VII of the Civil Rights Act.

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