Analytical Development Senior Research Scientist, Clinical Manufacturing Investigations

Vertex Inc. • Boston, MA

2d • Onsite

About The Position

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.

Requirements

• 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.
• 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.
• 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

Responsibilities

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

Benefits

• annual bonus
• annual equity awards
• medical, dental and vision benefits
• 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)

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 501-1,000 employees