Scientist, Analytical Development (Contract)

Vertex Pharmaceuticals; Boston (MA); On-site; USD 83,000 - 85,000; Full time

Job summary

Vertex Pharmaceuticals in Boston is seeking a Scientist, Analytical Development to support analytical strategy and method development for complex therapeutic programs, with emphasis on biologics and cell and gene therapy.

This role focuses on developing, optimizing, qualifying, and transferring analytical methods to characterize product quality, purity, identity, and stability, using HPLC, LC-MS, and biophysical techniques.

Qualifications

• Bachelor’s, Master’s, or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Molecular Biology, or a related scientific discipline
• Experience in analytical development and pharmaceutical/biotech development
• Strong hands-on experience with HPLC/UPLC and LC-MS
• Experience with biophysical characterization techniques (DLS, SEC-MALS, CE) is a plus
• Excellent data interpretation and cross-functional communication

Responsibilities

• Develop, qualify, and transfer analytical methods for characterization of therapeutic materials, intermediates, and final products
• Apply and troubleshoot analytical techniques including HPLC/UPLC, LC-MS, DLS, SEC-MALS, and CE
• Perform biophysical characterization to assess quality attributes such as purity, aggregation, size distribution, molecular weight
• Generate, analyze, interpret, and communicate analytical data to cross-functional teams
• Maintain documentation and support ELN usage

Skills

Analytical Chemistry

Biochemistry

Molecular Biology

Education

Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Molecular Biology (degree)

Tools

HPLC/UPLC

LC-MS

DLS

SEC-MALS

CE

Job description

Job Description

Scientist, Analytical Development

Position Summary

We are seeking a talented and highly motivated (Scientist), Analytical Development to support analytical strategy and method development for complex therapeutic programs, with an emphasis on biologics and cell and gene therapy. This individual will play a key role in developing, optimizing, qualifying, and transferring analytical methods used to characterize product quality, purity, identity, and stability.

The ideal candidate will have strong technical expertise in HPLC, LC-MS, and biophysical characterization techniques, including DLS, SEC-MALS, and CE, as well as the ability to work effectively in a cross-functional, fast-paced development environment.

Key Responsibilities

• Develop, optimize, qualify, and support transfer of analytical methods for characterization of therapeutic materials, intermediates, and final products
• Apply and troubleshoot analytical techniques including HPLC/UPLC, LC-MS, DLS, SEC-MALS, and CE
• Perform biophysical characterization to assess critical quality attributes such as purity, aggregation, size distribution, molecular weight, and heterogeneity
• Generate, analyze, interpret, and clearly communicate analytical data to cross-functional teams
• Support product and process development through analytical testing for comparability, formulation, stability, and process-related investigations
• Author and review technical documents including protocols, reports, method qualification summaries, and development reports
• Collaborate closely with partners in process development, manufacturing, quality, regulatory, and research functions
• Support collaboration activities with external contract organizations as needed
• Maintain accurate and complete documentation in accordance with applicable quality and compliance standards. Prior experience with Electronic Lab Notebook (ELN) documentation is preferred.

Required Qualifications

• Bachelor’s, Master’s, or PhD in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, Molecular Biology, or a related scientific discipline
• Relevant industry experience in analytical development, pharmaceutical development, biotechnology, or a related field
• Strong hand-on experience with HPLC/UPLC and LC-MS, including method development, optimization, and troubleshooting
• Prior experience with biophysical characterization techniques, including DLS, SEC-MALS, and CE is beneficial but not required
• Demonstrated ability to interpret complex analytical data and draw scientifically sound conclusions
• Strong written and verbal communication skills, with the ability to present findings clearly to technical and cross-functional audiences
• Strong organizational skills and ability to manage multiple priorities in a dynamic environment

Preferred Qualifications

• Experience supporting cell and gene therapy programs, biologics, or other advanced therapeutic modalities
• General knowledge of analytical considerations for complex biologics or cell and gene therapies
• Experience with analytical method qualification, comparability studies, stability studies, and technology transfer
• Familiarity with work in regulated environments, including GLP/GMP practices
• Proven ability to work collaboratively across multidisciplinary teams

Core Competencies

• Analytical rigor and scientific problem-solving
• Strong technical troubleshooting skills
• Attention to detail and commitment to data quality
• Effective cross-functional collaboration
• Clear communication and technical writing
• Ability to adapt in a fast-paced research and development environment

Pay Range

%60-$62/HR

Requisition Disclaimer

This job posting is for a temporary role with a third-party agency partner on assignment at Vertex Pharmaceuticals ("Vertex"). The individual selected for this role will be offered the role as an employee of a third-party agency partner; compensation, medical benefits, fringe benefits and other terms and conditions of employment shall be presented by the third-party agency partner upon offer. The pay rate range provided is a reasonable estimate of the anticipated compensation range for this job at the time of posting. The actual pay rate will be based on a number of factors, including skills, competencies, experience, location and/or being pursued and other job-related factors permitted by law.

No C2C or Third-Party Vendors