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Senior Method Transfer Scientist Jobs (NOW HIRING)

kindeva

Scientist III

Bridgeton, MO

The Analytical Development Scientist III functions as a senior technical expert within the QC organization, supporting analytical method transfer, verification, and validation activities for both ...

kindeva

Scientist III

Bridgeton, MO

The Analytical Development Scientist III functions as a senior technical expert within the QC organization, supporting analytical method transfer, verification, and validation activities for both ...

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Senior Method Transfer Scientist information

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$66.5K

$110.5K

$164.5K

How much do senior method transfer scientist jobs pay per year?

As of May 30, 2026, the average yearly pay for senior method transfer scientist in the United States is $110,545.00, according to ZipRecruiter salary data. Most workers in this role earn between $91,500.00 and $125,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Senior Method Transfer Scientist, and why are they important?

To thrive as a Senior Method Transfer Scientist, you need a strong background in analytical chemistry, method validation, and pharmaceutical sciences, typically supported by an advanced degree in a related field. Proficiency with laboratory instrumentation (such as HPLC, GC, and LC-MS), regulatory guidelines (e.g., ICH, FDA), and quality management systems is essential. Excellent project management, problem-solving, and communication skills help facilitate collaboration between cross-functional teams and external partners. These skills are crucial for ensuring seamless method transfers that meet regulatory standards and maintain product quality.

How does a Senior Method Transfer Scientist typically collaborate with cross-functional teams during technology transfer projects?

A Senior Method Transfer Scientist plays a key role in facilitating communication and coordination between analytical, manufacturing, and quality assurance teams during tech transfer projects. They are responsible for ensuring analytical methods are robustly transferred from development to manufacturing sites, often by organizing technical meetings, drafting transfer protocols, and troubleshooting discrepancies. Close collaboration is essential to address technical challenges and ensure regulatory compliance, making strong interpersonal and project management skills vital for success in this role.

What does a Senior Method Transfer Scientist do?

A Senior Method Transfer Scientist is responsible for overseeing the transfer of analytical methods between laboratories or from development to manufacturing settings, ensuring that the methods are robust, reproducible, and compliant with regulatory standards. They coordinate technical activities, troubleshoot issues during the transfer process, and document all procedures and results. This role often involves close collaboration with cross-functional teams, including quality assurance and regulatory affairs, to guarantee successful and efficient method implementation.

What is the difference between Senior Method Transfer Scientist vs Method Transfer Scientist?

AspectSenior Method Transfer ScientistMethod Transfer Scientist
Required CredentialsBachelor's or Master's in Pharmaceutical Sciences, Chemistry, or related field; 5+ years experienceBachelor's or Master's in relevant science; 2-5 years experience
Work EnvironmentPharmaceutical or biotech manufacturing, R&D labsSimilar settings, often involved in process development and manufacturing
Employer & Industry UsageUsed in large pharma, biotech companies, contract manufacturing organizationsCommon in similar industries, often as a stepping stone to senior roles

The Senior Method Transfer Scientist typically has more experience, responsibilities, and oversight in transferring manufacturing processes between sites or scales. The Method Transfer Scientist focuses on executing transfer activities under supervision, with less leadership responsibility. Both roles require strong technical knowledge, but the senior position involves greater project management and strategic planning.

Infographic showing various Senior Method Transfer Scientist job openings in the United States as of May 2026, with employment types broken down into 89% Full Time, and 11% Nights. Highlights an 100% In-person job distribution, with an average salary of $110,545 per year, or $53.1 per hour.
Scientist/Senior Scientist - Cell Bioassay/Potency

Scientist/Senior Scientist - Cell Bioassay/Potency

Frontage Laboratories

Exton, PA • On-site

$88.30K - $120.60K/yr

Full-time

Medical, Dental, Life, Retirement

Posted 5 hours 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.