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Bioassay Development Jobs in Pennsylvania (NOW HIRING)

The Research and Development Sciences (RaDS) value team in our company's Research & Development ... bioassays, as well as in vivo study data management, from animal management through safety ...

The individual is responsible for the technical aspects and programmatic oversite of the Bioassay ... for the development and maintenance of procedures related to radiological and radiological ...

Technician I Microbiology

Malvern, PA ยท On-site

$24.70/hr

... bioassays, viral clearance studies and stability and lot release programs, we support clients throughout the biologic development cycle, from the establishment and characterization of cell banks ...

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Bioassay Development information

See Pennsylvania salary details

$29.1K

$53.5K

$81.2K

How much do bioassay development jobs pay per year?

As of Aug 8, 2026, the average yearly pay for bioassay development in Pennsylvania is $53,546.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,600.00 and $60,100.00 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.
What job categories do people searching Bioassay Development jobs in Pennsylvania look for? The top searched job categories for Bioassay Development jobs in Pennsylvania are:
Infographic showing various Bioassay Development job openings in Pennsylvania as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 17% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $53,546 per year, or $25.7 per hour.

Scientist/Senior Scientist - Cell Bioassay/Potency

Frontage Laboratories

Exton, PA โ€ข On-site

$88K - $120K/yr

Full-time

Medical, Dental, Life, Retirement

Re-posted 9 days ago


Job description

Scientist/Senior Scientist - Cell Bioassay/Potency

Title: Scientist/Sr. Scientist, Cell Bioassay/Potency

Location: Exton, PA

Reports to: Sr Director BGC Therapy Operations

Full-time

Frontage Laboratories Inc. is an award winning, full-service, CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.


Position/Job Summary:

The Scientist/ Sr. Scientist will be a leading member in the Analytical Technologies group responsible for bioassay development, validation, transfer, and execution at Gritstone Bio. The bioassays include cell-based potency assay, ELISA, PCR-based assays, and virus infectivity assays, etc., that are used to support product characterization, release, stability study in GMP setting as well as other research projects for process, formulation, and manufacturing development. This position will contribute to the strategy of selecting and implementing bioassays to ensure our products are comprehensively characterized and under superb quality control. With dedication to troubleshooting and optimizing assays on bench, this position may lead a small group to achieve department goals. Excellent training and background in biological sciences, such as cell biology, molecular biology, biochemistry, immunology, virology, etc., is required.


Roles & Responsibilities:

  • Develop and apply molecular biological methods, immunoassays, and other state of the art analytical technologies to analyze and characterize cell and gene products, biotherapeutic proteins, their conjugates, and variants.
  • Independently select, develop, validate, and transfer biological assays including cell-based potency assays, ELIZA, qPCR-based assays, virus infectivity assays, etc.
  • Perform method development, validation, tech transfer, product characterization, impurity profiling, routine, and stability testing across varieties of biological products.
  • Prepare project proposals, protocols, reports, Certificate of Analysis, investigation reports, and generate cGMP documents.
  • Prepare and review notebooks in compliance with Frontage CMC SOPs.
  • Maintain qualification and compliance of instruments and conduct technical and instrumental troubleshooting.
  • Manage projects from initiation to completion and ensure the projects are on time and meeting pre-established quality standards.
  • Author method SOPs, development reports, qualification/validation reports to support method transfer to GMP QC
  • Perform analytical tests to support method development, DS/DP characterization, PD studies, lot release and stability testing of drug substance and drug products.
  • Development and optimization of analytical methods, in accordance with client requirements and associated protocol and procedures

Education, Experience & Skills Required:

Educational/Training Requirement:

  • PhD, MS or BS in Biological Science, Biochemical Engineering, or related discipline.


Experience:

  • PhD in Biological Science, Biochemical Engineering, or related discipline with 0-2 years’ relevant industrial GMP testing or analytical development experience for biologics or cell and gene therapy products, or
  • MS with 2-4 years’ GMP testing or analytical development experience for biologics or cell and gene therapy products, or
  • BS with 3-5 years’ GMP testing or analytical development experience for biologics or cell and gene therapy products.
  • Excellent organization and planning skills.
  • Experience in virus-vector based biotechnology or virology in general is preferred but not required.
  • Excellent communication skills, with the ability to work with individuals in wide ranging teams at all levels and the ability to lead and influence.

Salary and Benefits:

Frontage Laboratories offers a competitive compensation and benefits package including health and dental insurance, a 401(k) plan, disability insurance, and life insurance.

Frontage Laboratories Inc. is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, among other things, or status as a qualified individual with disability.