About this opportunity
Vertex Pharmaceuticals lists this Scientist, Analytical Development (Contract) opportunity in boston, Massachusetts. Review the employer’s description below for duties, qualifications and application requirements.
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
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Worksite address
boston, MA, 02298, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.