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Senior Assay Development Scientist Jobs in Spring, TX

SINOPEC Employee Position Overview Senior R&D Scientist The Senior R&D Scientist is responsible for advancing catalyst and catalytic process research at the SINOPEC-UOP Joint Research Center. This ...

Senior R and D Scientist

Katy, TX · On-site

$90K - $115K/yr

Senior R&D Scientist Department: SINOPEC-UOP Joint Research Center Employment: SINOPEC Employee Position Overview The Senior R&D Scientist is responsible for advancing catalyst and catalytic process ...

Senior R and D Scientist

Katy, TX · On-site

$120 - $180/hr

SINOPEC Employee Position Overview Senior R&D Scientist The Senior R&D Scientist is responsible for advancing catalyst and catalytic process research at the SINOPEC-UOP Joint Research Center. This ...

Senior Research Assistant

Houston, TX · On-site

$31.01 - $37.26/hr

... development and reducing the need for treatment. The Senior Research Assistant plays a critical ... Works closely with other lead scientists to execute the assays. Other duties as assigned Education ...

Senior Scientist

The Woodlands, TX · On-site

$81K - $111K/yr

The Senior Scientist for Chemical Enhanced Oil Recovery provides technical leadership for ... The position partners closely with internal R&D, technology, and commercial teams while mentoring ...

Senior Acoustic Scientist

Houston, TX · On-site

$87K - $119K/yr

Senior Acoustic Scientist Are you an expert with Sonic and UltraSonic? Do you enjoy developing ... Driving new manufacturing technology development and design for manufacturability To be successful ...

New

Senior Acoustic Scientist

Houston, TX · On-site

$87K - $119K/yr

Senior Acoustic Scientist Are you an expert with Sonic and UltraSonic? Do you enjoy developing ... Driving new manufacturing technology development and design for manufacturability To be successful ...

New

Senior Acoustic Scientist

Houston, TX · On-site

$140 - $190/hr

Senior Acoustic Scientist Are you an expert with Sonic and UltraSonic? Do you enjoy developing ... Driving new manufacturing technology development and design for manufacturability To be successful ...

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Showing results 1-20

Senior Assay Development Scientist information

See Spring, TX salary details

$59.2K

$98.4K

$146.4K

How much do senior assay development scientist jobs pay per year?

As of Sep 4, 2026, the average yearly pay for senior assay development scientist in Spring, TX is $98,373.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,400.00 and $111,200.00 per year, depending on experience, location, and employer.

What does a senior assay development scientist do?

A Senior Assay Development Scientist designs, optimizes, and validates biochemical or cell-based assays for research, diagnostics, or drug development. They lead assay development projects, troubleshoot technical challenges, and collaborate with cross-functional teams. Their role often includes analyzing experimental data, ensuring assay reproducibility, and maintaining compliance with regulatory standards. Additionally, they mentor junior scientists and contribute to scientific publications or regulatory submissions.

What are the key skills and qualifications needed to thrive as a senior assay development scientist?

A Senior Assay Development Scientist should possess advanced expertise in assay design, validation, and troubleshooting, supported by a degree in biochemistry, molecular biology, or a related field. Familiarity with laboratory automation platforms, high-throughput screening technologies, and software for data analysis such as Prism or SoftMax Pro is typically required. Strong project management, problem-solving, and cross-functional communication skills enhance effectiveness in leading projects and collaborating across departments. These skills are crucial for delivering robust, innovative assays that meet regulatory standards and support critical research or product development goals.

What are the typical challenges faced by a senior assay development scientist and how do they overcome them?

Senior Assay Development Scientists often encounter challenges such as optimizing assay sensitivity and specificity, troubleshooting inconsistent results, and meeting tight project timelines. To overcome these, they rely on deep scientific knowledge, rigorous method validation, and effective collaboration with other scientists, engineers, and quality assurance teams. Staying up to date on the latest technologies and regulatory requirements also helps address technical and compliance-related hurdles. By fostering open communication and drawing on multidisciplinary expertise within their teams, these professionals develop innovative solutions and ensure high-quality outcomes.

What are popular job titles related to Senior Assay Development Scientist jobs in Spring, TX?

For Senior Assay Development Scientist jobs in Spring, TX, the most frequently searched job titles are:

What cities near Spring, TX are hiring for Senior Assay Development Scientist jobs?

Cities near Spring, TX with the most Senior Assay Development Scientist job openings:

Associate Director, Assay Validation

Baylor Genetics

Houston, TX • On-site

$140 - $210/hr

Other

Re-posted 25 days ago


Key responsibilities

  • Lead the planning, design, and execution of analytical validation studies for sequencing-based assays.

  • Develop and maintain validation strategies, protocols, and reports that comply with regulatory and quality standards.

  • Analyze validation data and provide data-driven recommendations for assay optimization, issue resolution, and launch readiness.


Baylor Genetics rating

8.4

Company rating: 8.4 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

32nd of 121 rated laboratories


Job description

Location: Headquarters, Baylor Genetics, 2450 Holcombe Blvd, Houston, TX 77021, USA

Responsibilities
  • Lead the planning, design, and execution of analytical validation studies for sequencing‑based assays, including germline, somatic, and liquid biopsy applications.
  • Develop and maintain validation strategies, protocols, and reports that comply with CLIA, CAP, NYS, and internal quality standards.
  • Collaborate with Assay Development, Bioinformatics, Quality, and Product teams to align validation strategy with assay design, clinical claims, and product readiness.
  • Establish acceptance criteria, reference materials, and performance metrics to support analytical and clinical validation activities.
  • Serve as the subject matter expert for NGS validation methods, study design, assay performance characterization, and regulatory expectations.
  • Analyze validation data and provide data‑driven recommendations for assay optimization, issue resolution, and launch readiness.
  • Support regulatory or laboratory inspections and contribute to responses, documentation, or corrective action plans as needed.
  • Mentor scientists at different levels and contribute to building a scalable validation function within the R&D organization.
  • Maintain up‑to‑date knowledge of emerging trends, technologies, and regulatory guidance in NGS assay validation and clinical genomics.
  • Perform other duties as assigned to support team and organizational objectives.
  • Comply with all company policies, procedures, and applicable regulatory requirements.
Qualifications – Required
  • PhD in Molecular Biology, Genetics, Genomics, or a related discipline with 6+ years of relevant experience; or M.S. with 8+ years of experience in NGS assay development and validation.
  • Demonstrated track record leading validation of clinical NGS assays under CLIA, CAP, NYS, or equivalent regulatory frameworks.
  • Strong expertise in NGS library preparation, sequencing platforms, and assay performance characterization.
  • Deep understanding of analytical validation parameters, including accuracy, precision, limit of detection, specificity, reproducibility, and related statistical evaluation.
  • Experience collaborating with bioinformatics teams for pipeline verification and integrated assay validation.
  • Familiarity with quality management systems, design control, and documentation best practices.
  • Excellent problem‑solving, communication, and cross‑functional collaboration skills.
  • Proven ability to lead complex projects and influence without direct authority in a matrixed environment.
  • Equivalent combination of education and experience may be considered.
Preferred
  • Prior experience with germline clinical genetic testing or prenatal liquid biopsy testing.
  • Knowledge of NYS clinical test submission requirements or FDA IVD development processes.
  • Experience managing a small team.
  • Familiarity with automation or process scaling for NGS workflows.
Competencies
  • Scientific rigor and strong attention to detail.
  • Strategic thinking with hands‑on execution capability.
  • Collaborative mindset with strong communication across scientific and business functions.
  • Commitment to quality, compliance, and continuous improvement.
Physical Demands and Work Environment
  • Location: Houston, TX / Remote.
  • Work may be performed in an office, remote, and/or laboratory environment depending on business needs and assigned responsibilities.
  • May require exposure to standard laboratory conditions and adherence to applicable safety, quality, and regulatory requirements.
  • Must be able to use standard office equipment and computer systems for extended periods.
  • Travel requirements may vary based on business needs.
EEO Statement

Baylor Genetics is proud to be an equal opportunity employer committed to fostering an inclusive and diverse workplace. We welcome and encourage applicants from all backgrounds to apply. We do not discriminate on the basis of race, color, religion, national origin, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, pregnancy, childbirth, or any other status protected by applicable federal, state, or local law.

We are required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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