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Full Time Assay Development Scientist Jobs (NOW HIRING)

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How much do full time assay development scientist jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for full time assay development scientist in the United States is $38.99, according to ZipRecruiter salary data. Most workers in this role earn between $33.89 and $42.55 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Full Time Assay Development Scientist, and why are they important?

To thrive as a Full Time Assay Development Scientist, you need a strong background in biochemistry, molecular biology, or a related field, typically with an advanced degree (M.S. or Ph.D.) and experience in assay design and optimization. Familiarity with laboratory techniques such as ELISA, PCR, and data analysis software, as well as experience with laboratory information management systems (LIMS), is often required. Strong problem-solving skills, attention to detail, and effective communication are essential soft skills for collaborating with cross-functional teams and troubleshooting experiments. These skills are crucial for ensuring the development of robust, reliable assays that advance research and product development objectives.

What is the difference between Full Time Assay Development Scientist vs Research Associate?

AspectFull Time Assay Development ScientistResearch Associate
CredentialsBachelor's or Master's in Life Sciences, relevant experienceBachelor's or Master's in Life Sciences, entry-level experience
Work EnvironmentLaboratories focused on assay development and validationResearch labs supporting various projects, often assisting assay teams
Industry UsageCommon in biotech, pharma, and diagnostics companiesUsed across research institutions and biotech firms

The Full Time Assay Development Scientist typically has more specialized experience in designing and validating assays, working independently on development projects. In contrast, the Research Associate often supports research activities, assisting assay development under supervision. Both roles are essential in biotech and pharma industries, but the Scientist role involves greater responsibility and expertise in assay creation and optimization.

What are some common challenges faced by Full Time Assay Development Scientists during the transition from research to routine clinical or commercial assays?

Full Time Assay Development Scientists often encounter challenges when translating laboratory protocols into robust assays suitable for routine clinical or commercial use. These challenges can include optimizing assay reproducibility, ensuring consistent performance across different sample types, and meeting regulatory requirements. Scientists also need to collaborate closely with quality assurance, manufacturing, and regulatory teams to validate and document procedures. Overcoming these hurdles requires strong problem-solving skills, attention to detail, and effective cross-functional communication.

What is a Full Time Assay Development Scientist?

A Full Time Assay Development Scientist is a laboratory professional who specializes in designing, developing, and optimizing analytical assays for various scientific applications, such as drug discovery, diagnostics, or quality control. They work in research and development teams, conducting experiments, analyzing data, and troubleshooting assay protocols to ensure accuracy and reliability. Their role also involves documenting results, validating new methods, and collaborating with other scientists to support project goals. Typically, they have advanced degrees in biology, chemistry, or related fields and possess strong problem-solving and technical skills.
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What cities are hiring for Full Time Assay Development Scientist jobs? Cities with the most Full Time Assay Development Scientist job openings:
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What states have the most Full Time Assay Development Scientist jobs? States with the most job openings for Full Time Assay Development Scientist jobs include:

Analytical Development Senior Research Scientist, Imaging Assay Development

Vrtx

Boston, MA

$122K - $183K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 21 days ago


Job description

Job Description

General Summary:

We are seeking a highly motivated and experienced Senior Scientist to join our Analytical Development team. The successful candidate will play a critical role in the development, optimization, and transfer of imaging-based assays to automation platforms or quality control (QC) environments. This position requires a strong background in analytical development, imaging technologies, and assay automation, as well as a proven ability to work collaboratively in a cross-functional team environment.

Key Duties and Responsibilities:

  • Assay Development:

    • Design, develop, optimize, qualify/validate imaging-based assays to support drug development and manufacturing processes.
    • Evaluate and implement advanced imaging technologies to enhance assay sensitivity, specificity, and throughput.
    • Develop robust and reproducible methods for quantitative image analysis.
  • Technology Transfer:
    • Lead the transfer of imaging-based assays to automation platforms or QC environments, ensuring compliance with regulatory requirements and industry standards.
    • Collaborate with cross-functional teams, including automation engineers, quality assurance, and manufacturing, to ensure seamless assay implementation.
    • Provide technical support and training to QC teams for assay execution and troubleshooting.
  • Data Analysis and Interpretation:
    • Analyze and interpret complex imaging data to support decision-making in product development and quality control.
    • Develop and qualify/validate data analysis pipelines and algorithms for imaging-based assays.
  • Documentation and Compliance:
    • Author and review technical documents, including protocols, reports, and standard operating procedures (SOPs).
    • Ensure compliance with regulatory guidelines (e.g., FDA, ICH, USP) and internal quality standards.
  • Collaboration and Leadership:
    • Act as a subject matter expert (SME) for imaging-based assays within the organization.
    • Mentor and train junior scientists and research associates.
  • Collaborate with cross-functional teams, including research, process development, and quality assurance, to support project goals.

Knowledge and Skills:

Required:

  • Understanding of analytical development for biologics, cell and genetic therapy products
  • Image-based assay expertise: IHC, IF
  • Experience or knowledge in confocal microscopy, and image-based high throughput instruments (e.g. Opera, Operetta, CX7 and FlowCam)
  • Strong knowledge of imaging technologies, image acquisition, and analysis software (e.g., ImageJ, CellProfiler, or similar tools).
  • Technical expertise in mammalian cell culture, and cell based assays.
  • Ability to multi-task as necessary, managing competing priorities and advancing multiple projects within required timelines
  • Strong communication skills and a willingness to reach out across teams to accomplish program goals
  • Familiar with regulatory (FDA, ICH, USP, etc) guidance surrounding analytical assay development for cell based assays.
  • Experience working collaboratively across teams to achieve analytical development goals
  • Participation on global development teams(s) where contributions are made to form CMC strategy is preferred

Preferred:

  • Strong background in analytical method development, qualification, validation and tech transfer for cell therapy product.
  • A background in stem cell biology, experience with stem cell (ESC, iPSC) derived cell therapy product.
  • Familiar with regulatory guidance and experience with regulatory filing for CGT products

Other: Flexible team player excited to collaborate with internal and external partners.

Education and Experience:

  • Ph.D. in Biology, Cell biology, Biochemistry or a related field with 3-5+ years of relevant industry experience, or M.S. with 5+ years of relevant industry experience, or a BS/BA with 8+ years of relevant industry experience.
  • Proven expertise in developing and optimizing imaging-based assays (e.g., fluorescence microscopy, high-content imaging, or other imaging modalities).
  • Experience with assay transfer to automated platforms or QC environments is highly desirable.
  • Preferred: 3+ years of relevant industry experience in the cell and gene therapy analytical assay development.

Pay Range:

$122,400 - $183,600

Disclosure Statement:

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations. From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation:

On-Site Designated

Flex Eligibility Status:

In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertex's Policy on Flex @ Vertex Program and may be changed at any time.

#LI-Onsite

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at ApplicationAssistance@vrtx.com