ZipRecruiter

Log In

1

Ada Assay Development Jobs (NOW HIRING)

Actalent

PK/ADA Scientist

Auxvasse, MO · On-site

Demonstrated experience developing PK or ADA assays from scratch, including method development and validation. * In-depth knowledge of regulatory agency guidelines, general SOPs, and excellent ...

Actalent

PK/ADA Scientist

Auxvasse, MO · On-site

Demonstrated experience developing PK or ADA assays from scratch, including method development and validation. * In-depth knowledge of regulatory agency guidelines, general SOPs, and excellent ...

next page

Showing results 1-20

All JobsBusiness JobsCommunications JobsCommunications Specialist JobsAda Assay Development Jobs

Ada Assay Development information

See salary details

$20

$38

$61

How much do ada assay development jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for ada assay development in the United States is $38.66, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $46.15 per hour, depending on experience, location, and employer.

What is an ADA Assay Development scientist?

An Ada Assay Development scientist is a specialist who designs, develops, and validates assays—laboratory tests—for detecting and quantifying anti-drug antibodies (ADA) in biological samples. These assays are crucial in biopharmaceutical development to monitor immune responses against therapeutic proteins and ensure drug safety and efficacy. The role involves working with various technologies, optimizing assay conditions, and interpreting data to support regulatory submissions and clinical trials.

What are the key skills and qualifications needed to thrive as an ADA Assay Development scientist?

To excel in ADA Assay Development, you need a solid background in immunology, biochemistry, and assay design, usually supported by a degree in biological sciences or a related field. Familiarity with bioanalytical platforms such as ELISA, ECL, and Luminex, as well as knowledge of regulatory guidelines (e.g., FDA, EMA), is crucial. Strong analytical thinking, attention to detail, and effective communication are vital soft skills for interpreting results and collaborating across multidisciplinary teams. These competencies ensure the accurate detection of anti-drug antibodies, which is critical for drug safety and regulatory compliance.

What are the typical challenges faced by professionals working in ADA Assay Development, and how can they be addressed?

Professionals in ADA (Anti-Drug Antibody) assay development often encounter challenges such as optimizing assay sensitivity and specificity, minimizing matrix interference, and ensuring reproducibility across samples. Regulatory expectations for assay validation and documentation can also be demanding. Addressing these challenges involves staying updated with the latest industry guidelines, collaborating closely with cross-functional teams like bioanalytical scientists and regulatory affairs, and continuously refining assay protocols based on feedback and testing results.

What is the difference between Ada Assay Development vs Laboratory Technician?

AspectAda Assay DevelopmentLaboratory Technician
CredentialsBachelor's or higher in life sciences, specialized training in assay developmentAssociate's or bachelor's in science, technical training
Work EnvironmentResearch labs, biotech companies, pharmaceutical firmsClinical, research, or manufacturing labs
Industry UsageUsed in biotech, pharma, and research institutions for assay creationSupports lab operations, sample processing, and testing

While Ada Assay Development focuses on designing and optimizing assays for research and development, Laboratory Technicians perform routine testing and sample analysis. Both roles are essential in biotech and pharma industries but differ in scope, responsibilities, and required expertise.

What are popular job titles related to Ada Assay Development jobs?

For Ada Assay Development jobs, the most frequently searched job titles are:

Infographic showing various Ada Assay Development job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 92% In-person, and 8% Remote job distribution, with an average salary of $80,420 per year, or $38.7 per hour.

Scientist, Method Development - Ligand Binding Assays

Lincoln, NE • On-site

Celerion
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees
Learn more about Celerionexternal

$30.75 - $38.50/hr

Full-time

Re-posted 14 days ago

Celerion rating

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

Job description

Celerion is committed to swift, exceptional clinical research through translational medicine. Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.
Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!
Celerion is seeking a Scientist to join our Ligand Binding Assay Development team. The successful candidate will have strong problem-solving skills, scientific expertise and knowledge in Ligand Binding bioanalytical method development.
This full-time role is located at our Lincoln, NE facility.
As a Scientist, Method Development, you will provide scientific expertise and method development skills to the Ligand Binding Assay Development group at Celerion. A key component of the role is to provide innovation and change management required to remain on the cutting edge of Ligand Binding Bioanalytical Sciences.
Responsibilities:
  • Undertake original and innovative research and techniques that include developing ligand binding assays utilizing state-of-the-art technologies for the rapid and accurate analysis of protein/peptides/ antibodies in biological matrices
  • Perform assays (pharmacokinetics (PK), pharmacodynamics PD)/biomarkers, ADA) according to regulatory and quality systems
  • Analyze and interpret data, generate summary tables, and troubleshoot assay performance, as well as peer-review raw data for accuracy and completeness
  • Work effectively within a team and across teams to meet objectives under time constraints
  • Support the associate director in achieving challenging business objectives for the method development team. Includes innovation, change management, evaluation of new technology, and growth in market share, revenue, profit, and customer loyalty.
  • Develop methods by applying and interpreting scientific theories, concepts, techniques, and regulatory requirements in bioanalytical studies
  • Provide technical/scientific guidance and leadership to study teams, as well as other areas of the company to ensure project completion in a timely manner
  • Author scientific manuscripts for publication in peer-reviewed journals and present research findings through posters and oral presentations at scientific conferences
  • Participate and provide technical expertise during client calls and visits

Requirements:
  • Minimum of a Bachelor's degree in Biochemistry, Chemistry or Biology required. An advanced degree is preferred.
  • 5+ years of related scientific experience preferred; CRO/industry experience is a plus
  • The candidate must have proven proficiency in immunoassay development and be capable of working on multiple projects simultaneously
  • Strong hands-on experience in at least one of the following pharmacokinetics (PK), pharmacodynamics (PD)/biomarkers, ADA assay development
  • Understanding of FDA and ICH guidelines in method validation and sample analysis
  • Prior experience working in a regulated GLP-compliant environment is preferred
  • Experience in one or more immunoassay techniques (Ligand Binding assay: ELISA, MSD, Gyrolab, AlphaLISA)
  • Experience using Watson LIMS is preferred
  • Excellent verbal and technical writing skills and be capable of presenting to an audience of researchers from a variety of disciplines
  • Ability to work well with a team and with staff in other locations effectively

Celerion Values: Integrity Trust Teamwork Respect
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

What Celerion employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply