Senior Scientist, Analytical Development- Mutagenic Impurities

Posted 4 Days Ago
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Boston, MA
7+ Years Experience
Biotech • Pharmaceutical
The Role
Seeking a talented scientist to become a subject matter expert in mutagenic impurity control within the Drug Substance Control Strategy team. Responsibilities include developing test methods, collaborating with project teams, authoring publications, and maintaining accurate records. Must have a strong understanding of mutagenic impurities, organic chemistry, analytical techniques, and relevant work experience in analytical chemistry.
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Job Description

General Summary:

Vertex is seeking a talented scientist eager to help develop both cutting-edge small molecule pharmaceuticals and the science underpinning the analytical control of their syntheses.

This scientist will become a subject matter expert (SME) in mutagenic impurity within the Drug Substance Control Strategy team in Analytical Development this role will support small molecule drug development programs at Vertex.

The position will focus on understanding the pathways for mutagenic impurity formation and contributing to the design and execution of studies. The Sr. Scientist will also work on developing test methods for characterizing potential risk factors in collaboration with other members of analytical development, such as the control strategy, trace analysis, and chromatography SME teams. Additionally, the position will involve authoring internal and external publications to support the safe and rapid advancement of new drugs.

Candidates with an understanding of small molecule pharmaceutical process development, and modern analytical techniques will be best equipped to succeed in this role.

Key Duties and Responsibilities:

  • Serve as subject matter expert for mutagenic impurity control and advance science-driven understandings of their formation, prevention, and rejection.
  • Develop, troubleshoot, and execute a broad range of test methods to characterize mutagenic impurity risk factors in pharmaceutically relevant matrices.
  • Collaborate closely with project teams and partner organizations to deliver timely solutions across a portfolio of projects
  • Author and present results in both oral and written reports.
  • Maintains accurate records of experiments and results in an electronic laboratory notebook.
  • Complies with applicable SOPs.
  • Performs other duties as assigned.

Knowledge and Skills:

  • Understanding of current science on the formation and control of mutagenic impurities, particularly nitrosamines.
  • Foundational knowledge of organic chemistry is essential along with an understanding of drug substance and drug product process development.
  • Experience developing and running analyses relevant to small molecule characterization (HPLC, GC, IC, KF, etc.).
  • The ability to design and conduct experiments independently with minimal supervision is essential.
  • The ability to work successfully in both a team/matrix environment as well as independently is essential.
  • The ability to work in a fast-paced environment, manage priorities, and maintain timelines for multiple projects is essential.
  • Excellent written and verbal communication skills as demonstrated by symposia presentations and research publications in peer reviewed journals are required.

Education and Experience:

  • Degree in physical sciences or engineering is required along with relevant work experience in analytical chemistry.
  • Ph.D. and 2-5 year of relevant employment experience, or an MSc and 5+ years of relevant employment experience, or a BSc and 8+ years of relevant experience

In this On-Site designated role, you will work five days per week on-site with ad hoc flexibility.

#LI-Onsite

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, sex, gender identity or expression, age, religion, national origin, ancestry, ethnicity, disability, veteran status, genetic information, sexual orientation, marital status, or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager, or contact Talent Acquisition at [email protected].

The Company
HQ: Boston, MA
5,000 Employees
Hybrid Workplace
Year Founded: 1989

What We Do

Vertex is a global biotechnology company that invests in scientific innovation to create transformative medicines for people with serious and life-threatening diseases.

We discovered and developed the first medicines to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease. In addition to clinical development programs in CF, Vertex has more than a dozen ongoing research programs focused on the underlying mechanisms of other serious diseases.

Founded in 1989 in Cambridge, Massachusetts, our corporate headquarters is now located in Boston’s Innovation District, and our international headquarters is in London, United Kingdom. We currently employ approximately 3,500 people in the United States, Europe, Canada, Australia and Latin America with nearly two-thirds of our staff dedicated to research and development.

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. Our research and medicines have also received esteemed recognitions, including the Robert J. Beall Therapeutics Development Award, the French Prix Galien and the British Pharmacological Society awards.

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