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Bioassay Development Jobs (NOW HIRING)

Alcami Corporation

Sr. Scientist I - Bioassay

Durham, NC · On-site

$82K - $113K/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 ...

Revvity

Sr. Scientist, Bioassay

San Diego, CA · On-site

$122K - $162K/yr

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 ...

Alcami Corporation

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 ...

Eurofins Scientific

Bioassay Analyst

Indianapolis, IN · On-site

... Development and Manufacturing Organisations. It also has a rapidly developing presence in highly ... Perform cell-based bioassays and surrogate bioassays such as ligand-binding ELISA assays in plate ...

Eurofins

Bioassay Analyst

Indianapolis, IN · On-site

... Development and Manufacturing Organisations. It also has a rapidly developing presence in highly ... Perform cell-based bioassays and surrogate bioassays such as ligand-binding ELISA assays in plate ...

Revvity

Sr. Scientist, Bioassay

San Diego, CA

$122K - $162K/yr

Job Summary BioLegend is seeking a Bioassay Scientist to join the Molecular and Cellular Biology ... Work across functional groups to facilitate new product development * Maintain scientific knowledge ...

Eurofins Scientific

Scientist - Bioassay

Columbia, MO

$33.50 - $42/hr

Eurofins BPT-Columbia is looking for a Scientist to join our growing Bioassay team located in ... Responsibilities include completing work for research and development under CGMP and/or GLP ...

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Bioassay Development information

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$29K

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How much do bioassay development jobs pay per year?

As of Jul 16, 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.
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What states have the most Bioassay Development jobs? States with the most job openings for Bioassay Development jobs include:
What job categories do people searching Bioassay Development jobs look for? The top searched job categories for Bioassay Development jobs are:
Bioassay Development jobs near you
Infographic showing various Bioassay Development job openings in the United States as of July 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 100% In-person job distribution, with an average salary of $53,418 per year, or $25.7 per hour.
Sr. Scientist I - Bioassay

Sr. Scientist I - Bioassay

Alcami Corporation

Durham, NC • On-site

$82K - $113K/yr

Full-time

Re-posted 3 days ago

Alcami rating

7.3

Company rating: 7.3 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

At Alcami, we deliver reliable solutions that unlock the potential of transformative medicines from discovery to commercialization, through trusted partnership with our clients, recognized industry expertise and proven regulatory track record.
Are you interested in joining our team?
Job Summary
The Senior Scientist I, Bioassay is accountable for driving results in a fast-paced environment by performing routine and non-routine testing in support of pharmaceutical product development and manufacturing. 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 potency assays, ELISA, real-time PCR, enzymatic activity assays, binding kinetic assays and other biochemical testing methods. Strong problem-solving and troubleshooting skills along with proficiency in analyzing data, laboratory documentation, data presentation and collaboration will help ensure success in this position.
On-Site Expectations
  • 100% on-site position.
  • 1st Shift: Monday - Friday, 8:30am - 5:30pm.

Responsibilities
  • Performs laboratory analysis of pharmaceutical and biopharmaceutical products utilizing analytical instrumentation, analyzes and documents data in accordance with Alcami SOPs.
  • Documents results in electronic laboratory notebook.
  • Performs one or more of the following techniques: cell-based potency assays, ELISA, real-time PCR, enzymatic activity assays, binding kinetic assays and other biochemical testing methods
  • Supports troubleshooting and problem solving activities for cell-based and biochemical tests.
  • Evaluates and interprets generated data.
  • Contributes to operational initiatives to support continued growth of the organization.
  • Develops and validates biological tests to determine purity, identity, and potency of pharmaceutical and biopharmaceutical products.
  • Writes standard operating procedures (SOPs), test procedures, specifications, and summary reports.
  • Maintains working knowledge of instrumentation, equipment, and scientific methodologies necessary to perform assigned tasks.
  • Assists in removal of hazardous waste, routine equipment cleaning, and restocking of consumable products and reagents.
  • Interacts with team members, management, and clients to discuss data and project progress.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Effectively uses various laboratory software packages (SoftMax, ProCal, Master Control, ELN, etc.).
  • Maintains a safe, clean, and organized work environment free of safety hazards.
  • Safely handles potent compounds.
  • Ensures timely completion and compliance with cGMP and all other relevant company training requirements.
  • Other duties as assigned.

Qualifications
  • Bachelor's degree and 8+ years of related experience.
  • OR Master's degree with 4+ years of related experience.
  • OR PhD with 2+ years of experience required.
  • 2+ years of experience in Pharmaceutical, CDMO, or cGMP required.

Knowledge, Skills, and Abilities
  • Working knowledge of peptides, monoclonal antibodies, recombinant proteins is required, and knowledge of cell therapy and gene therapy is preferred.
  • Expert knowledge of Cell-based Bioassays required.
  • Expert knowledge of ELISA/immunoassays required.
  • Strong knowledge of Enzymatic Activity Assays preferred.
  • Strong knowledge of Laboratory Documentation is required.
  • Strong knowledge of cGMP in a pharmaceutical or regulated environment is required.
  • Strong verbal communications and presentation skills required.
  • Strong time management and organization skills required.
  • Strong knowledge of Laboratory equipment and safety required.
  • Strong problem solving and trouble shooting ability required.
  • Proficiency with Microsoft Office (Word, Excel, PowerPoint) required.
  • Working knowledge of SoftMax preferred.

Travel Expectations
  • Up to 5% travel required.

Physical Demands and Work Environment
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this Job, the employee is regularly required to use hands to finger, handle, or feel; reach with hands and arms; talk or hear and smell. The employee is frequently required to sit. The employee is occasionally required to stand; walk and stoop, kneel, crouch, or crawl. The employee must regularly lift and/or move up to 10 pounds, frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, distance vision, color vision, peripheral vision, depth perception and ability to adjust focus. While performing the duties of this Job, the employee is occasionally exposed to moving mechanical parts and vibration. The noise level in the work environment is usually very quiet.
While performing the duties of this job, the employee is frequently exposed to moving mechanical parts, fumes or airborne particles and toxic or caustic chemicals. The employee is occasionally exposed to wet and/or humid conditions; high, precarious places; risk of electrical shock and vibration. The noise level in the work environment is usually moderate. The employee will be required to wear the appropriate personal protective equipment for specific job duties to be performed. Such personal protective equipment may include, but not limited to safety eyewear, hearing protection, various types of respirators/breathing apparatus, lab coats, full protective body coverings, various types of gloves, etc. Other tasks involving elevated work may require the use of a body harness and lanyard. Additionally, the employee may be required to operate an industrial vehicle.

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