Analytical Development Senior Research Scientist, Clinical Manufacturing Investigations

Reposted 4 Days Ago
Be an Early Applicant
Boston, MA, USA
In-Office
122K-184K Annually
Mid level
Biotech • Pharmaceutical
The Role
The role involves leading technical investigations in clinical manufacturing, resolving quality issues, driving continuous improvement, and collaborating across teams in cell therapy programs.
Summary Generated by Built In

Job Description

General Summary:

Vertex is seeking a highly skilled and motivated Analytical Development Senior Research Scientist to join our team. This role is critical in ensuring the success of clinical manufacturing processes for our cell therapy programs by leading technical investigations, resolving quality events, and driving continuous improvement in analytical development. The ideal candidate will possess a strong scientific background, excellent problem-solving skills, and the ability to collaborate effectively across cross-functional teams.

Key Duties and Responsibilities:

  • Technical Support and Investigations:

    • Act as the primary point of contact for technical support related to clinical run investigations.

    • Troubleshoot technical issues, perform in-depth root cause analyses, and develop hypotheses to address challenges.

    • Design and execute hypothesis-driven test protocols to identify and resolve technical issues.

    • Prepare comprehensive technical reports summarizing findings, conclusions, and recommendations.

  • Investigation Leadership:

    • Lead and facilitate investigation meetings with cross-functional teams, including manufacturing, quality control, quality assurance, and analytical development.

    • Collaborate with technical Subject Matter Experts (SMEs) to develop and implement effective investigation strategies.

    • Drive timely resolution of technical issues to ensure the expedited release of drug products.

  • Cross-Functional Communication and CAPA Implementation:

    • Serve as a liaison between manufacturing, quality control, quality assurance, and analytical development teams to address and resolve quality events.

    • Develop and implement Corrective and Preventive Actions (CAPA) to mitigate risks and prevent recurrence of issues.

    • Ensure timely communication and alignment across all stakeholders to maintain compliance and operational efficiency.

  • Data Management and Analysis:

    • Oversee the management and analysis of analytical product characterization and method development datasets from clinical runs.

    • Utilize electronic systems for sample and data management, ensuring accurate data trending and reporting.

  • Flexibility and Commitment:

    • Provide support for critical projects, including occasional weekend or late-night work, to meet organizational deadlines and ensure project success.

Knowledge and Skills:

  • Technical Expertise:

    • Proficiency in a wide range of analytical platforms used for product characterization and release assays, particularly in the cell and gene therapy space.

    • Strong working knowledge of manufacturing and quality systems to support quality events, analytical investigations, and the development of corrective and preventive actions.

    • Experience with electronic systems for sample and data management, as well as data trending and analysis.

  • Skills and Competencies:

    • Exceptional problem-solving abilities with a methodical and analytical approach to technical challenges.

    • Strong cross-functional communication and collaboration skills to effectively engage with diverse teams.

    • Proficiency in good documentation practices to ensure compliance with regulatory and quality standards.

Education and Experience:

  • Ph.D. (or equivalent degree) and 2-5 years of relevant post-doctoral employment experience, or

  • Masters Degree (or equivalent degree) and 5+ years of relevant employment experience, or

  • Bachelors Degree (or equivalent degree) and 7+ years of relevant employment experience

Pay Range:

$122,400 - $183,600

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.

#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]

Skills Required

  • Ph.D. and 2-5 years relevant experience, or Masters Degree and 5+ years experience, or Bachelors Degree and 7+ years experience
  • Proficiency in analytical platforms for product characterization
  • Experience with electronic systems for data management
  • Strong problem-solving and analytical skills
  • Excellent cross-functional communication skills
  • Good documentation practices

Vertex Pharmaceuticals Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Vertex Pharmaceuticals and has not been reviewed or approved by Vertex Pharmaceuticals.

  • Parental & Family Support Policies provide 12 weeks of 100% paid bonding leave for all U.S. parents with additional fully paid time for birth parents. Family-forming supports include adoption and surrogacy assistance, fertility options like IVF and egg cryopreservation, breast‑milk shipping, subsidized childcare, backup care, and a DCFSA match.
  • Leave & Time Off Breadth Time off includes roughly four weeks of vacation, 13 holidays, sick time, and two companywide shutdowns (summer and year‑end). Some roles also include flexible or unlimited time off and paid volunteer time.
  • Retirement Support Programs include a 401(k) plan with employer contributions and an employee stock purchase plan. Filings describe employer contributions occurring in company stock, supporting long‑term ownership.

Vertex Pharmaceuticals Insights

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The Company
HQ: Boston, MA
5,000 Employees
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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