Scientist, Analytical Development (Contract)
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Vertex Pharmaceuticals
Boston, MA, US
Summary
The scientist will develop, optimize, and qualify analytical methods to characterize therapeutic materials, including biologics and cell and gene therapies. They will also interpret complex analytical data and collaborate with cross-functional teams to support product development and stability studies.
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 hands-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. In addition, this role will be eligible for overtime pay, in accordance with federal and state requirements
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No C2C or Third-Party Vendors
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases and has made significant advancements in cystic fibrosis, sickle cell disease, transfusion-dependent beta thalassemia, and acute pain — and continues to progress clinical and research programs in these diseases. We also have a robust clinical pipeline of investigational therapies across a range of modalities in other serious diseases where we have deep insight into causal human biology, including acute and neuropathic pain, APOL1-mediated kidney disease, IgA nephropathy, autosomal dominant polycystic kidney disease, type 1 diabetes and myotonic dystrophy type 1.
Our global headquarters is in Boston, and we have research and development (R&D) sites and commercial offices worldwide.
Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. We have also earned a spot on TIME Most Influential Companies, TIME Best Inventions, and Fast Company Most Innovative Companies lists. Our research and medicines have received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the Prix Galien, the Scrip Award and the Breakthrough Prize awards.
Read our community guidelines: https://www.vrtx.com/vertexs-community-guidelines/
Founded
1989
Company size
5,001-10,000 employees
Industry
Biotechnology
Org type
Public Company
Headquarters
Boston, MA
Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious diseases and has made significant advancements in cystic fibrosis, sickle cell disease, transfusion-dependent beta thalassemia, and acute pain — and continues to progress clinical and research programs in these diseases. We also have a robust clinical pipeline of investigational therapies across a range of modalities in other serious diseases where we have deep insight into causal human biology, including acute and neuropathic pain, APOL1-mediated kidney disease, IgA nephropathy, autosomal dominant polycystic kidney disease, type 1 diabetes and myotonic dystrophy type 1.
Our global headquarters is in Boston, and we have research and development (R&D) sites and commercial offices worldwide.
Vertex is consistently recognized as one of the industry’s top places to work by Science Magazine, The Boston Globe, Boston Business Journal and the San Diego Business Journal. We have also earned a spot on TIME Most Influential Companies, TIME Best Inventions, and Fast Company Most Innovative Companies lists. Our research and medicines have received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the Prix Galien, the Scrip Award and the Breakthrough Prize awards.
Read our community guidelines: https://www.vrtx.com/vertexs-community-guidelines/
Founded
1989
Company size
5,001-10,000 employees
Industry
Biotechnology
Org type
Public Company
Headquarters
Boston, MA