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Bioassay Development Jobs (NOW HIRING)

Sr. Automation Engineer

Norwood, MA · On-site

$117K - $154K/yr

Lead the development and hardening of automated bioassay workflows, transforming early-stage prototypes into robust, scalable, GMP-ready systems * Collaborate with scientists to translate cell-based ...

Sr. Automation Engineer

Norwood, MA · On-site

$117K - $154K/yr

Lead the development and hardening of automated bioassay workflows, transforming early-stage prototypes into robust, scalable, GMP-ready systems * Collaborate with scientists to translate cell-based ...

Direct and oversee bioassay development, screening, and hit validation efforts. * Manage compound isolation, purification, and structure elucidation workflows in collaboration with analytical and ...

Job Summary At BioLegend, this position contributes to new product development by performing bioassays to evaluate recombinant proteins and neutralizing antibodies. Primary responsibilities include ...

Find your future at Revvity Job Summary At BioLegend, this position contributes to new product development by performing bioassays to evaluate recombinant proteins and neutralizing antibodies.

Find your future at Revvity Job Summary At BioLegend, this position contributes to new product development by performing bioassays to evaluate recombinant proteins and neutralizing antibodies.

Bioassay GMP scientist will interact with other departments to maintain continuous project flow ... Follow design and development process under current GMP guidelines * Prepare documents required for ...

Job Title Sr. Scientist, Bioassay Location(s) San Diego - BioLegend About Us Revvity is a developer ... Work across functional groups to facilitate new product development * Maintain scientific knowledge ...

Sr. Scientist I - Bioassay

Wilmington, NC · On-site

$83K - $114K/yr

The Sr. Scientist I, Bioassay may also be required to work on method development and method validation projects. The Senior Scientist I, Bioassay will demonstrate strong knowledge in cell-based ...

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Bioassay Development information

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$29K

$53.4K

$81K

How much do bioassay development jobs pay per year?

As of Jun 5, 2026, the average yearly pay for bioassay development in the United States is $53,418.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,500.00 and $60,000.00 per year, depending on experience, location, and employer.

What is bioassay development?

Bioassay development is the process of designing, optimizing, and validating biological tests (bioassays) that measure the potency, purity, or biological activity of a substance, such as a drug, vaccine, or biologic. These assays are crucial in pharmaceutical and biotechnology industries for quality control, regulatory approval, and research. The process involves selecting the appropriate biological system, establishing assay conditions, and ensuring reproducibility and accuracy of results.

What are some typical challenges faced during bioassay development, and how are they addressed within a team setting?

A common challenge in bioassay development is ensuring assay reproducibility and robustness across different batches and operators. Teams often address this by conducting thorough validation studies, standardizing protocols, and encouraging open communication to troubleshoot issues quickly. Collaboration between scientists, statisticians, and quality control personnel is essential to optimize assay conditions and interpret data accurately. Regular team meetings and documentation help keep everyone aligned and maintain high assay performance standards.

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

To thrive as a Bioassay Development Scientist, you need a strong background in molecular biology, biochemistry, and analytical techniques, typically supported by a degree in life sciences or a related field. Familiarity with laboratory automation, data analysis software (such as GraphPad Prism or SoftMax Pro), and regulatory guidelines like GLP/GMP is essential. Attention to detail, critical thinking, and strong collaboration skills help you design robust assays and solve complex problems effectively. These competencies are vital for generating reliable data, ensuring compliance, and advancing drug discovery or quality control processes.
More about Bioassay Development jobs
What states have the most Bioassay Development jobs? States with the most job openings for Bioassay Development jobs include:
Infographic showing various Bioassay Development job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 97% Full Time, and 2% Contract. Highlights an 98% Physical, 1% Hybrid, and 1% Remote job distribution, with an average salary of $53,418 per year, or $25.7 per hour.
Sr. Automation Engineer

Sr. Automation Engineer

Moderna Therapeutics

Norwood, MA • On-site

$117K - $154K/yr

Full-time

Medical, PTO

Posted 22 days ago


Moderna rating

8.8

Company rating: 8.8 out of 10

Based on 8 frontline employees who took The Breakroom Quiz

11th of 71 rated pharmaceutical


Job description

The Role:

Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.

Moderna is strengthening its presence in Norwood, Massachusetts, a cornerstone of our manufacturing and operational excellence. Our Norwood campus translates mRNA science into scalable impact, supporting the global delivery of our medicines. We welcome talent ready to drive innovation and make a meaningful difference for patients worldwide.

In this role, you will operate at the intersection of automation engineering and bioassay development, transforming early-stage automation into robust, scalable, GMP-ready systems that enable high-throughput, reliable bioassay execution.
As a Senior Engineer I, you will lead the technical execution of automation solutions that preserve biological integrity while meeting stringent regulatory, data integrity, and operational requirements.
Working as an individual contributor in a 100% onsite environment in Norwood, you will collaborate cross-functionally while leveraging advanced digital tools and Generative AI to optimize automation performance, enhance traceability, and drive scalable assay workflows.

Here's What You'll Do:

  • Lead the development and hardening of automated bioassay workflows, transforming early-stage prototypes into robust, scalable, GMP-ready systems

  • Collaborate with scientists to translate cell-based bioassays and sample preparation workflows into automation solutions, accounting for biological constraints such as cell health, sterility, and timing sensitivity

  • Design and implement automation strategies for cell handling workflows (e.g., maintenance, passaging, transfection, assay execution) to ensure reproducibility and assay integrity at scale

  • Own technical execution across projects, including requirements definition, system integration, testing, deployment, and sustainment

  • Partner cross-functionally with Analytical Development, Applied Technologies, Analytical Sciences & Technology, Digital, and QC Operations to enable successful transfer and deployment of systems into regulated environments

  • Develop automation solutions that meet GMP expectations, including data integrity, traceability, and audit readiness

  • Troubleshoot complex issues across biological performance, liquid handling, and system integration layers, including investigation of assay variability and automation-induced bias

  • Drive standardization and continuous improvement of automation platforms and workflows to support scalability across programs

The key Moderna Mindsets you'll need to succeed in the role:

"We digitize everywhere possible using the power of code to maximize our impact on patients."

"We act with urgency; Action today compounds the lives saved tomorrow."

Here's What You'll Bring to the Table (Basic Qualifications)

  • BS with 8 years of relevant experience, MS with 5 years of relevant experience or PhD in Engineering, Biology, Biochemistry, Bioengineering, or related discipline.

  • Hands-on experience supporting or working with cell-based bioassays or sample preparation workflows.

  • Experience working in or supporting regulated laboratory environments. (GLP/GMP)

  • Experience programming and developing with laboratory automation software/hardware and liquid handlers.

  • This position is site-based, requiring you to be at Moderna's site full-time. This position is not eligible for remote work.

Here's What You'll Bring to the Table (Preferred Qualifications)

  • Experience supporting or deploying automation systems into GMP or regulated environments, including:

    • Validation support (IQ/OQ/PQ)

    • Change control and lifecycle management

    • Documentation aligned with regulatory expectations

  • Experience developing and supporting automation for:

    • Mammalian cell culture workflows (maintenance, passaging, expansion)

    • Transfection or cell treatment processes

    • Plate-based bioassay sample preparation workflows (e.g. ELISA)

  • Experience with 3rd party automation hardware such as cobot arms, decappers, centrifuges, dispensers, sealers/peelers, etc.

  • Direct experience configuring and optimizing Hamilton STAR/Vantage automated liquid handling systems.

  • Experience with workcell based automation equipment controlled by scheduling software such as HighRes Cellario, Thermo CRS Momentum, etc.

  • Success Characteristics

  • Demonstrates strong ownership and accountability; delivers high-quality, reliable outcomes

  • Collaborates effectively across functions; proactively solves complex problems

Pay & Benefits

At Moderna, we believe that when you feel your best, you can do your best work. That's why our US benefits and global well-being resources are designed to support you-at work, at home, and everywhere in between.

  • Best-in-class healthcare coverage, plus voluntary benefit programs to support your unique needs

  • A holistic approach to well-being, with access to fitness, mindfulness, and mental health support

  • Family planning benefits, including fertility, adoption, and surrogacy support

  • Generous paid time off, including vacation, volunteer days, sabbatical, global recharge days, and a discretionary year-end shutdown

  • Savings and investment opportunities to help you plan for the future

  • Location-specific perks and extras

The salary range for this role is $121,600.00 - $194,500.00. This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An individual's position within the salary range will be based on several factors including, but not limited to, specific competencies, relevant education, qualifications, certifications, experience, skills, performance, and business or organizational needs. The successful candidate may be eligible for an annual discretionary bonus, other incentive compensation, or equity award, subject to company plan eligibility criteria and individual performance.

About Moderna

Since our founding in 2010, we have aspired to build the leading mRNA technology platform, the infrastructure to reimagine how medicines are created and delivered, and a world-class team. We believe in giving our people a platform to change medicine and an opportunity to change the world.

By living our mission, values, and mindsets every day, our people are the driving force behind our scientific progress and our culture. Together, we are creating a culture of belonging and building an organization that cares deeply for our patients, our employees, the environment, and our communities.

We are proud to have been recognized as a Science Magazine Top Biopharma Employer, a Fast Company Best Workplace for Innovators, and a Great Place to Work in the U.S.

If you want to make a difference and join a team that is changing the future of medicine, we invite you to visit modernatx.com/careers to learn more about our current opportunities.

Our Working Model

As we build our company, we have always believed an in-person culture is critical to our success. Moderna champions the significant benefits of in-office collaboration by embracing a 70/30 work model. This 70% in-office structure helps to foster a culture rich in innovation, teamwork, and direct mentorship. Join us in shaping a world where every interaction is an opportunity to learn, contribute, and make a meaningful impact.

Moderna is a smoke-free, alcohol-free, and drug-free work environment.

Equal Opportunities

Moderna 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 or citizenship, ethnicity, disability, military or protected veteran status, genetic information, sexual orientation, marital or familial status, or any other personal characteristic protected under applicable law.Moderna is a place where everyone can grow. If you meet the Basic Qualifications for the role and you would be excited to contribute to our mission every day, please apply!

Moderna is an E-Verify Employer in the United States. We consider qualified applicants regardless of criminal histories, consistent with legal requirements.

Accommodations

We're focused on attracting, retaining, developing, and advancing our employees. By cultivating a workplace that values diverse experiences, backgrounds, and ideas, we create an environment where every employee can contribute their best.

Moderna is committed to offering reasonable accommodations to qualified job applicants with disabilities. 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 contact the Accommodations team at leavesandaccommodations@modernatx.com.

Export Control Notice This position may involve access to technology or data that is subject to U.S. export control laws, including the Export Administration Regulations (EAR). As such, employment is contingent upon the applicant's ability to access export-controlled information in accordance with U.S. law. Due to the nature of the work and regulatory requirements, only individuals who qualify as U.S. persons (citizens, permanent residents, asylees, or refugees) are eligible for this position. For this role Moderna is unable to sponsor non-U.S. persons to apply for an export control license. #LI-TR2

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Moderna logo

About Moderna

Sourced by ZipRecruiter

In just over a decade, Moderna has evolved from a research-focused company in the messenger RNA (mRNA) field to a leading enterprise with a diverse clinical portfolio of vaccines and therapeutics. With a strong intellectual property portfolio and state-of-the-art manufacturing capabilities, Moderna collaborates with global partners to advance groundbreaking science and achieve rapid scaling of production. Notably, Moderna's mRNA platform has enabled the development of therapies for various diseases, including infectious diseases, immuno-oncology, and cardiovascular conditions. Recognized as a top biopharmaceutical employer, Moderna fosters an inclusive and smoke-free work environment. The company is dedicated to equal employment opportunities and non-discrimination, ensuring that all employees and applicants are treated with respect and without bias based on factors like race, gender, religion, disability, or sexual orientation. Moderna is also committed to providing reasonable accommodations for individuals with disabilities, in accordance with applicable laws. To know more, visit www.modernatx.com.

Industry

Manufacturing

Company size

501 - 1,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

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