Analytical Development Senior Research Scientist, Clinical Manufacturing Investigations

Vertex Pharmaceuticals Inc

Boston, MA

JOB DETAILS
SALARY
$122,400–$183,600 Per Year
SKILLS
Analysis Skills, Analytical Development, Assays, Biotech and Pharmaceutical, Continuous Improvement, Corrective Action, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Data Analysis, Data Management, Data Quality, Data Sets, Drug Development, Drug Release, Gene Therapy, Identify Issues, Legal, Maintain Compliance, Manufacturing, Manufacturing Systems, Manufacturing/Industrial Processes, Problem Solving Skills, Process Improvement, Quality Assurance, Quality Control, Risk Management, Root Cause Analysis, Scientific Research, Team Player, Technical Leadership, Technical Support, Testing, Time Management, Trend Analysis
LOCATION
Boston, MA
POSTED
30+ days ago

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 ApplicationAssistance@vrtx.com

About the Company

V

Vertex Pharmaceuticals Inc

Vertex is a global biotechnology company that aims to discover, develop and commercialize innovative medicines so people with serious diseases can lead better lives. In addition to our clinical development programs focused on cystic fibrosis, Vertex has more than a dozen ongoing research programs aimed at other serious and life-threatening diseases. Founded in 1989 in Cambridge, Mass., Vertex today has research and development sites and commercial offices in the United States, Europe, Canada and Australia. For six years in a row, Science magazine has named Vertex one of its Top Employers in the life sciences. For additional information and the latest updates from the company, please visit www.vrtx.com
COMPANY SIZE
5,000 to 9,999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
FOUNDED
1989
WEBSITE
https://www.vrtx.com/