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Vertex Pharmaceuticals

Senior Scientist Analytical Development – Molecular-based assays - Automation & Testing

Posted 4 Days Ago
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In-Office
Boston, MA
124K-187K Annually
Senior level
In-Office
Boston, MA
124K-187K Annually
Senior level
The Senior Scientist leads molecular-based assay development and automation for gene therapy programs, ensuring efficiency and compliance. Responsibilities include assay design, data analysis, and mentoring junior staff.
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Job Description

General Summary:

The Analytical Development Senior Research Scientist consistently demonstrates a high level of strategic planning and experimental execution, working within established timelines. Works with a high degree of independence and demonstrates the ability to lead a team, either formally or informally, to achieve experimental and organizational goals. Takes a leading role in writing documents (method documents, protocols, reports) and demonstrates high-level analytical skills and understanding of data interpretation. Actively seeks cross-functional roles to improve communication between groups and achieve efficiency in achieving organizational deliverables.

Key Duties and Responsibilities:

  • Evaluate and develop molecular-based assays to evaluate DNA, genome integrity, and RNA characteristics to support characterization and release assays for identity, purity, strength, and potency for Vertex cell and gene therapy programs.
  • Develop, qualify, and implement novel high-throughput (HTP) and/or automated assays for various molecular-based assays, such as ddPCR, qPCR, Nanostring, microarray, and NGS, for biologics or cell and gene therapy.
  • Provide manual and automated routine analytical testing for various assays related to cell and gene therapy to support process development, process characterization, and others
  • Work closely with Analytical Development and Research teams to translate the manual or LTP based into HTP and an automated method.
  • Perform HTP and automated assay qualification to establish specificity, sensitivity, linear range, precision, and accuracy of test methods.
  • Develop assay design criteria using Design of Experiments (DOE) and other contemporary development tools.
  • Transfer assays to QC or external partners as needed.
  • Serve as SME for molecular-based assays across cell and gene therapy programs.
  • Enhance data visualization, reporting, and decision making by incorporating novel data automation techniques with python, R, JMP and other software.
  • Troubleshoot, optimize, and trend assay performance. Manage analytical reagents inventory, including reference standard materials as per regulatory standards.
  • Maintain excellent written documentation of completed experiments (ELN, LIMS) and maintain knowledge share systems (MS-Teams and SharePoint).
  • Generate all training procedures for users to ensure the smooth operation of the test method.
  • Be a strong team player, contributing to group priorities and deliverables. Training and mentoring junior team members.
  • Involved in IND and BLA filings as needed
  • Manage and supervise 2-3 contractors

Required Knowledge and Skills:

  • Expertise in nucleic acid-based assays development, such as ddPCR, qPCR, Nanostring, FISH, scRNA sequencing, and other NGS methods for cell and gene therapy.
  • Expertise in robotic liquid handlers (Hamilton, TECAN, or other) and their operating software (VENUS, Fluent Gx, or other) for automated sample preparation.
  • Experience with multiplexing molecular assays.
  • Experience with various data analysis and visualization software such as Python, R, PowerBI, JMP
  • Proven understanding of cell culture techniques, especially for embryonic stem cells (ESC) and induced pluripotent stem cells (iPSC).
  • Experience with other cell and gene therapy assays, such as flow cytometry, immune-based, and cellular-based assays, is a plus.
  • Understanding of bioprocessing, cell and gene therapy process development, characterization, and manufacturing.
  • Ability to use literature to design proof-of-concept studies.
  • Experienced in writing technical documents, including development reports, qualification protocols, and qualification reports.
  • Excellent communication and presentation skills with the proven ability to solve complex problems and to work effectively as a member of a multidisciplinary team, detail-oriented, multitasking, goal-oriented, timeline-oriented, and a critical thinker.
  • Team player, innovative, collaborative, and an initiator.
  • Ability to work and collaborate in a fast-paced environment with a high level of independence to manage projects

Education and Experience:

  • PhD in Biochemistry, Chemical Engineering, Cell & Molecular Biology, or related discipline with 3+ years of industry or academic experience

#LI-onsite #LI-SV1

Pay Range:

$124,400 - $186,500

Disclosure Statement:

The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, experience, and other job-related factors permitted by law.

At Vertex, our Total Rewards offerings also include inclusive market-leading benefits to meet our employees wherever they are in their career, financial, family and wellbeing journey while providing flexibility and resources to support their growth and aspirations.  From medical, dental and vision benefits to generous paid time off (including a week-long company shutdown in the Summer and the Winter), educational assistance programs including student loan repayment, a generous commuting subsidy, matching charitable donations, 401(k) and so much more.

Flex Designation:

On-Site Designated

Flex Eligibility Status:

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

Note: The Flex status for this position is subject to Vertex’s Policy on Flex @ Vertex Program and may be changed at any time.

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]

Top Skills

Ddpcr
Fluent Gx
Jmp
Microarray
Nanostring
Ngs
Python
Qpcr
R
Robotic Liquid Handlers
Venus
HQ

Vertex Pharmaceuticals Boston, Massachusetts, USA Office

Vertex Pharmaceuticals Inc., 50 Northern Avenue, Boston, MA 02210, US, Boston, MA, United States, 02210

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