Manager, Analytical Science & Technology - ASAT (Contract)

Vertex, Inc.
Boston, MA, United States
11 days ago
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Role details

Contract type
Temporary contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Compensation
$85,000.0 - $120,000.0
Working hours
Regular working hours

Tech stack

Microsoft Excel Data Analysis Databases Data Validation Information Engineering Data Integrity Data Mining Data Visualization Instant Messaging Technology Minitab Power BI JMP (Statistical Software)
+2 more
Statistics Packages Spotfire

Job description

Manager, Analytical Science & Technology (ASAT), will support analytical lifecycle management activities for commercial Cell and Gene Therapy (CGT) products within the Commercial Manufacturing & Supply Chain (CMSC) organization. This role will focus on analytical data verification, trending, mining, and interpretation to support commercial manufacturing, product lifecycle management, regulatory submissions, and health authority interactions. The successful candidate will have a strong understanding of analytical testing methodologies and data analysis, with demonstrated experience supporting CTD/eCTD Module 3 documentation and regulatory submissions., * Lead analytical data verification, trending, and data mining activities across commercial manufacturing, stability, process validation, and product lifecycle management programs.

  • Compile, review, and analyze analytical datasets to identify trends, investigate anomalies, and support scientific conclusions.
  • Generate statistical analyses, data visualizations, summaries, and technical assessments to support internal decision-making and regulatory submissions.
  • Collaborate with Analytical Development, Quality, Manufacturing, Regulatory Affairs, MSAT, and external laboratories to collect, assess, and interpret analytical data.
  • Author and review technical reports, data summaries, scientific justifications, and regulatory support documents.
  • Support preparation, review, and lifecycle maintenance of CTD/eCTD Module 3 content, including analytical methods, specifications, validation summaries, stability data, comparability assessments, and post-approval changes., By applying for this position, you agree to the Atrium Terms and Conditions and you direct Atrium to share your application materials, which may include your CV/Resume, email address or phone number, with Vertex. For more information on how Vertex handles your personal data related to your job application, please see Vertex’s Agreeing to the Atrium Terms and Conditions, includes permission to use the email address and mobile phone number you provide during the application process or throughout the duration of your prospective or actual employment to notify you of job openings, profiles, articles, news, and other employment-related information, as well as to notify you of special promotions or additional products and services offered by us or our affiliates and partners (collectively, “Atrium Alerts”). Atrium Alerts may be sent by email, phone, or text message. Your personal information will be safely stored within the Atrium & Vertex databases. Atrium does not sell your personal information to third parties. Text message and data rates may apply. To OPT OUT of text messaging or to modify your communication preferences for Atrium Alerts at any time, please contact Atrium at . If you do not agree with the Atrium Terms and Conditions, you can still complete your application for this position by emailing your resume to our team at Please include the job title in the subject of your email. No C2C or Third-Party Vendors, The Product Manager, Marketing Technology is responsible for leading the development and optimization of marketing technology solutions that enhance customer experience across both…

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Requirements

  • Strong understanding of analytical methods commonly used for biologics and/or cell and gene therapy products.
  • Ability to critically evaluate analytical data and understand assay capabilities, limitations, variability, and performance characteristics.
  • Demonstrated experience with data verification, data integrity review, trend analysis, and data mining.
  • Strong technical writing with attention to detail and excellent organizational and communicational skills.
  • Experience using JMP, Excel, Power BI, Spotfire, Minitab, or similar analytical and statistical tools.
  • Familiarity with GMP requirements, data integrity principles, ICH guidelines, and global regulatory expectations.
  • Ability to manage multiple projects and prioritize competing deadlines in a fast-paced environment.

Education and Experience:

  • B.S or above in Biology, Biochemistry, Analytical Chemistry and related fields.
  • Minimum 5 years of experience in the pharmaceutical/biopharmaceutical industry or the equivalent combination of education and experience.

Benefits & conditions

  • $136,200-204,200 per year

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